Head and neck
Published: 2024-05-14
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Systematic review of minimally-invasive reconstructive options for oral cavity defects

Department of Otolaryngology-Head and Neck Surgery, Hospital of Bolzano (SABES-ASDAA), Teaching Hospital of the Paracelsus Medical Private University (PMU), Bolzano, Italy
Department of Otolaryngology-Head and Neck Surgery, Hospital of Bolzano (SABES-ASDAA), Teaching Hospital of the Paracelsus Medical Private University (PMU), Bolzano, Italy
Department of Otolaryngology-Head and Neck Surgery, University Hospital of Verona, Verona, Italy
Department of Otolaryngology-Head and Neck Surgery, Hospital of Bolzano (SABES-ASDAA), Teaching Hospital of the Paracelsus Medical Private University (PMU), Bolzano, Italy
Department of Otolaryngology-Head and Neck Surgery, University Hospital of Verona, Verona, Italy. Corresponding author - virginia.dallari@gmail.com
Department of Otolaryngology-Head and Neck Surgery, University Hospital of Ferrara, Ferrara, Italy
Department of Otolaryngology-Head and Neck Surgery, Hospital of Bolzano (SABES-ASDAA), Teaching Hospital of the Paracelsus Medical Private University (PMU), Bolzano, Italy
Department of Otolaryngology-Head and Neck Surgery, Hospital of Bolzano (SABES-ASDAA), Teaching Hospital of the Paracelsus Medical Private University (PMU), Bolzano, Italy
Department of Otolaryngology-Head and Neck Surgery, Hospital of Bolzano (SABES-ASDAA), Teaching Hospital of the Paracelsus Medical Private University (PMU), Bolzano, Italy
Department of Otolaryngology-Head and Neck Surgery, Niguarda Hospital, Milan, Italy
Department of Otolaryngology-Head and Neck Surgery, Hospital of Bolzano (SABES-ASDAA), Teaching Hospital of the Paracelsus Medical Private University (PMU), Bolzano, Italy
oral cavity cancer oral cavity reconstruction local flaps Bichat’s flap palatal flap nasolabial flap

Abstract

The oral cavity is a primary site for malignant neoplasms of the head and neck region. Surgery, with or without adjuvant therapy, offers the highest probability of cure by focusing on radical tumour removal and organ function restoration. Reconstructive options are represented by local and free flaps, while small defects can be managed without reconstruction. For medium-sized defects without bone involvement, local flaps can be a good alternative to free flaps in selected patients. The purposes of this article are to analyse the main minimally-invasive reconstructive techniques in oral cancer surgery through a systematic review of the literature and develop a reconstructive algorithm based on the site and size of the defect. We defined minimally-invasive reconstruction as any reconstructive option not involving flap dissection from the neck or other distant areas from the oral cavity. Options considered include: local myo-mucosal or mucosal flaps (based on the facial or buccal arteries, and palatal flap), Bichat’s fat pad flap, and nasolabial flap. Use of biological or synthetic materials is also described. In selected patients with small to moderate-sized defects, the possibility of reconstruction with local flaps can be a viable option.

Introduction

The oral cavity is a primary site for malignant neoplasms in the head and neck region, with the majority being squamous cell carcinoma. Surgery, with or without adjuvant (chemo)radiotherapy, offers the highest probability of cure 1,2. Surgical goals include radical tumour removal and restoration of organ function. Key functional aspects encompass speech, tongue mobility, swallowing, oral competence, and separation of the oral cavity from the nose and neck 3.

Reconstructive options are represented by local, loco-regional, and free flaps. Small defects can be managed without reconstruction 4. In these cases, the use of synthetic materials promote healing and aid postoperative pain control. For medium-sized defects without bone involvement, local flaps are good reconstructive alternatives to microvascular free flaps. For locally advanced tumours, free flaps are the most viable option 5, while loco-regional flaps (such as the pectoralis major or temporalis flap) are used in selected cases, for example, in patients not eligible for reconstruction with a microvascular flap or salvage reconstruction. The purpose of this article is to analyse the main minimally-invasive reconstructive techniques in oral cancer surgery through a systematic review of the literature and develop an algorithm based on the defect’s site and size.

Methods

This systematic review was designed using the PICO search strategy for qualitative questions and written in accordance with the PRISMA statement. We defined minimally-invasive reconstruction as any reconstructive option not involving flap dissection from the neck or other distant areas from the oral cavity. We included the following options: local myo-mucosal or mucosal flaps (flaps based on the facial or buccal arteries, and palatal flaps), Bichat’s fat pad flap, local skin flaps (nasolabial flap), and reconstructive options using biological or synthetic materials.

The literature search was conducted on October 1, 2023, in the PubMed database using the following search strings (“famm flap”[All Fields]) OR (“facial artery musculo-mucosal flap”[All Fields] OR “facial artery musculo-mucosal”[All Fields] OR “facial artery musculo-mucosal famm flap”[All Fields] OR “facial artery musculo-mucosal flap”[All Fields] OR “facial artery musculo-mucosal”[All Fields] OR “facial artery myo-mucosal flap”[All Fields] OR “facial artery myo-mucosal island flap”[All Fields] OR “facial artery myo-mucosal island”[All Fields] OR “facial artery musculo-mucosal flaps”[All Fields] OR “facial artery musculo-mucosal famm”[All Fields] OR “facial artery myo-mucosal”[All Fields]) AND ((((“cancer”[All Fields])) OR (neoplasm) OR (carcinoma)))); ((((((((((“buccinator flap”[All Fields] OR “buccinator flap procedure”[All Fields] OR “buccinator muscle”[All Fields] OR “buccinator musculo-mucosal flap”[All Fields] OR “buccinator musculo-mucosal”[All Fields] OR “buccinator musculo-mucosal flaps”[All Fields] OR “buccinator musculo-mucosal flap”[All Fields] OR “buccinator musculo-mucosal”[All Fields] OR “buccinator myo-mucosal”[All Fields] OR “buccinator myo-mucosal flap”[All Fields] OR “buccinator musculo-mucosal island”[All Fields] OR “Bozola flap”[All Fields])))))))))) AND ((((“cancer”[All Fields])) OR (neoplasm) OR (carcinoma)))); ((((“palatal muco-periosteal flap”[All Fields] OR “palatal muco-periosteal flaps”[All Fields])) OR (“palatal flap”[All Fields])))) AND ((((“cancer”[All Fields])) OR (neoplasm) OR (carcinoma)))); “nasolabial flap”[All Fields] OR “nasolabial flap reconstruction”[All Fields] OR “nasolabial flaps”[All Fields] AND ((((“cancer”[All Fields])) OR (neoplasm) OR (carcinoma)))) AND (Oral Cavity);(((((“Bichat”[All Fields]) OR (“buccal fat pad”[All Fields])) OR (“Bichat fat pad”[All Fields])))) AND ((((“cancer”[All Fields])) OR (neoplasm) OR (carcinoma)))) AND (Oral Cavity))))).

The reference lists of the articles identified were reviewed and cross-referenced to identify any additional relevant articles.

The inclusion criteria for the studies were as follows:

  1. original articles published after January 1, 2000;
  2. articles including patients reconstructed with one of the following techniques: local mucosal or myo-mucosal flaps, local skin flaps, and Bichat’s flap;
  3. articles written in English, Italian, or German;
  4. articles comprising at least 5 patients who met the inclusion criteria;
  5. patients aged 16 years or older undergoing oncologic surgery of the oral cavity;
  6. presence of adequate data on defect location, reconstruction, and outcomes.

The exclusion criteria used were as follows:

  1. articles written in a language other than Italian, English, or German;
  2. case reports or case series with fewer than 5 patients, meta-analyses, or systematic literature reviews;
  3. articles on anatomical dissections;
  4. patients with oral cavity defects due to non-oncologic surgery (traumatic, benign pathology, infectious diseases);
  5. lack of sufficient data.

In the initial phase of the study, abstracts were selected for inclusion by two different authors (LG and VD). Full texts of the selected abstracts were then reviewed in detail. Only publications that clearly described the purpose and objectives, inclusion and exclusion criteria, with clear statistical data, reporting information on the surgical defect, success rates, and postoperative complications, were included. Eligibility for inclusion of the full-text articles was independently assessed by the same two above mentioned authors and, in case of uncertainty, discussed and decided by consensus.

For each reconstructive option, we collected key characteristics, various surgical flap preparation techniques, defect dimensions and locations, and any specific indications or contraindications.

Results

With the selected search criteria, 280 articles were found in the PubMed database. Six abstracts were added from the bibliography of the articles included, for a total of 286 articles examined. Seven articles were discarded because written in a language other than English, Italian, or German. The remaining 279 abstracts were reviewed by 2 different authors. After excluding case reports, case series with fewer than 5 patients, and patients operated on for non-malignant conditions, 67 articles published from January 1, 2000 until the search date were included for full-text review. Of these, 25 articles were discarded for the above-mentioned exclusion criteria. In the end, a total of 42 studies were included in our systematic review, as depicted in the PRISMA flow diagram (Fig. 1).

A total of 1322 patients were included. We categorised the articles into multiple groups based on the described local flap: facial artery-based flaps (facial artery myo-mucosal and Zhao flaps), buccinator flap (Bozola), palatal flap, nasolabial flap, and Bichat’s fat pad flap. Additionally, we considered reconstructive options with synthetic materials and non-reconstruction (Tab. I).

Myo-mucosal flaps pedicled on the facial artery

Regarding myo-mucosal flaps based on the facial artery, 15 articles with a total of 353 patients were included (Tab. II). Various techniques for harvesting buccinator flap were described: facial artery myo-mucosal (FAMM) flap, reverse flow FAMM flap with superior pedicle, facial artery myo-mucosal island flap (FAMMIF) or Zhao flap. The majority of patients presented with a defect in the oral floor, followed by the tongue, and, in some cases, reconstruction involved both the hard and soft palate. Defect sizes were specified in 5 articles (ranging from an average of 3.7x2.1 cm to 5.4x3.1 cm). In 6 articles, the defect size was described but precise measurements were not reported (but all defects were defined as small to medium-sized). Use of bite blocks in the early postoperative days was described in 2 articles. One study documented 4 cases of patients with double FAMM flaps.

Myo-mucosal flap based on the buccal artery

With regard to buccinator muscle flap, 5 articles were included, covering a total of 138 patients. The majority of patients presented defects in the tongue, oral cavity, palate, and buccal mucosa. Defect sizes were specified in only 2 of 5 articles, and ranged from 2 to 5 cm (Tab. III).

Palatal flap

Regarding the palatal flap, 6 articles were selected, involving a total of 175 patients. Most had a defect in the hard palate, while one study described its use for retromolar trigone and another for reconstruction of complex defects of the oral cavity. The defect sizes were specified in only one study (Tab. IV).

Fibroadipose Bichat’s flap

Regarding Bichat’s flap, 8 articles were included, involving a total of 156 patients. Most patients had a defect in the hard palate or buccal mucosa, while some patients had defects in other oral cavity sites such as the retromolar trigone. The defect sizes were specified in 6 of 8 articles, ranging from 3x1.5 cm to 5.5x4 cm (Tab. V).

Local skin flap: the nasolabial flap

Regarding local skin flaps, the only flap that met the inclusion criteria was the nasolabial flap. Eight articles related to such a surgical technique were included in the review, involving a total of 500 patients. Most patients had a defect in the tongue and oral pelvis, followed by the upper and lower gingiva, lip, buccal mucosa, vestibule, palate, and retromolar trigone. The defect sizes were specified in only 4 of 8 articles (Tab. VI).

Discussion

The reconstruction of defects resulting from oral cavity oncologic surgery is often imperative, not only for aesthetic reasons but primarily for functional purposes. The primary goal of reconstruction is to ensure the separation of the oral cavity from other anatomical spaces, avoiding salivary fistula and infection 4. Secondly, it aims to restore the function of the affected subsite, ensuring an acceptable quality of life. The optimal method for oral cavity reconstruction depends on various factors such as site, type, and amount of tissue to be replaced. The gold standard in reconstructing complex oral cavity defects is currently achieved through microvascular free flaps. However, this may not always be the best option due to donor site morbidity, need to explore the neck for vessels receiving the anastomosis, and, especially, the prolonged operative times, which may not be tolerable for patients with compromised systemic conditions and significant comorbidities. Additionally, it requires considerable expertise and often a double surgical team. In selected cases of patients with medium- or small-sized mucosal defects that do not require extensive reconstruction, where there is no need for resection connecting the oral cavity and the neck, or for patients who cannot tolerate prolonged anaesthesia, a viable reconstructive option is provided by local flaps 5. We will discuss the results obtained from the literature review, highlighting the advantages and disadvantages of each of these flaps.

Myo-mucosal flap pedicled on the facial artery

The initial account of a FAMM flap for head and neck reconstruction was reported by Pribaz and colleagues 6. Zhao et al. subsequently introduced a variation of this flap design, known as the FAMMIF 7. In the literature, there is much confusion regarding the nomenclature of these two flaps, and often the abbreviations are used ambiguously. The FAMM flap is an axial flap centred around the facial artery, featuring an oblique orientation that extends from the retromolar trigone to the ipsilateral gingiva-labial sulcus at the level of the alar margin. It can be pedicled either in a downward direction (with anterograde arterial flow) or upward (with reverse arterial flow or RFAMM), depending on the specific reconstructive requirements (Fig. 2) 7.

RFAMM can be employed to close defects in the anterior hard palate, maxillary alveolus, nasal septum, and upper lip. In contrast, when the FAMM flap is pedicled in a downward direction, it is particularly suitable to close defects in the posterior hard palate, soft palate, lower lip, mandibular alveolar region, and vestibule 8.

The FAMMIF is a variant of the FAMM flap, firstly described by Zhao in 1999. Employing this approach allows for the elevation of nearly the entire cheek mucosa as an independent island flap. While the angiosome of the buccal artery is removed, it is consistently incorporated into the flap to enhance peripheral vascularisation 9. This flap is a valuable choice to reconstruct defects in the palate, pharynx, tongue, and floor of the mouth. It consists of mucosal, submucosal, and buccinator muscle tissues. The FAMMIF is particularly suitable to address small to moderate defects in the oral cavity and oropharynx, while larger or composite defects still primarily rely on revascularised free flaps as the gold standard reconstructive option 10. More specifically, the FAMMIF is recommended for small to moderate defects (following the resection of T1-T2 tumours). In general, the FAMMIF is well-suited for addressing defects ranging from 4 to 10 cm in size, especially when there is the need for reconstructing with thin, flexible mucosal tissue closely matching the texture of the tissue removed 10.

It is worth considering a significant adaptation of the FAMMIF flap: the tunneled facial artery myo-mucosal island flap (t-FAMMIF). It is harvested on the inner side of the cheek, traverses a neck tunnel, and then enters the pharynx or oral cavity through a second tunnel. It offers an extensive range of rotation, making it possible to reconstruct nearly every region within the oral cavity and oropharynx, including those on the opposite side 9.

The FAMM flap offers numerous advantages. To begin with, it is a thin and flexible flap that adheres to the “replace like with like” principle. It involves a relatively brief dissection phase. The donor site morbidity is minimal, and it does not result in any external scar. Furthermore, prior radiation therapy in the area of the flap is not a contraindication for its use, since it maintains its integrity even after radiation 11.

Nevertheless, it also presents certain drawbacks. In dentate patients, the FAMM flap necessitates tooth extraction or use of a bite block during the healing process and a second surgical procedure for pedicle section 9,10. Regarding the t-FAMMIF, thoroughly dissecting the facial vessels and establishing tunnels between the mandible and cheek, as well as between the neck and the oral cavity, enable the flap to be repositioned independently from the dentition, eliminating the necessity for additional procedures to divide the pedicle 10. Additionally, while the FAMM has a broad range of rotation and a favourable length-to-base ratio (5:1), these factors can still pose limitations for more extensive and anterior tongue reconstructions, as well as for defects on the contralateral side 11.

Neither FAMM nor FAMMIF are recommended when there is widespread dysplasia in the oral cavity. However, as reported by Ferrari et al., if it is performed carefully and adjuvant radiotherapy is administered as usual when indicated, neck dissection with preservation of the facial artery and vein does not alter the rate of regional recurrences, confirming the oncologic safety of these flaps in oral cavity reconstruction 12. Both flaps address surgical defects within a short timeframe. There is no need for specific microvascular training or preoperative vascular evaluation. Moreover, morbidity is generally low, with flap dehiscence being the most commonly observed postoperative complication 10.

Myo-mucosal flap based on the buccal artery

The buccinator myo-mucosal flap is an axially vascularised flap that can be based on the facial or buccal arteries. It comprises the buccal mucosa and buccinator muscle, a thin muscle that forms the scaffolding of the cheek. It originates from the external surface of the alveolar processes of the mandible and maxillary bone last three molars. Posteriorly, it originates from the pterygomandibular raphe and attaches anteriorly to the orbicularis oris muscle. Laterally, it contacts the ramus of the mandible, masseter, medial pterygoid muscle, Bichat’s bulla, and the buccopharyngeal fascia. Medially, it is covered by the cheek submucosa and mucosa 30.

Regarding its vascularisation, the buccal, facial, and posterosuperior alveolar arteries constitute the main blood supply to the muscle. The buccal artery is a branch of the internal maxillary artery and vascularises the posterior half of the muscle. It runs antero-inferiorly under the lateral pterygoid muscle to reach the posterior half of the muscle, where it anastomoses with the posterior vestibular branch of the facial artery. The facial artery runs around the lower border of the mandible at the anterior margin of the masseter muscle. It supplies numerous branches to the buccinator muscle, the largest of which is the posterior buccal, which vascularises the posterior half of the muscle. The facial artery gives one to three inferior buccal branches to supply the lower half of the muscle, then continues in an anterosuperior direction to give off 3-5 small anterior buccal branches to the anterior half of the muscle. The posterosuperior alveolar artery, collateral of the internal maxillary artery, supplies two small branches to the muscle, which enter it posteriorly and superiorly, and the infraorbital artery gives off some small branches that enter it antero-superiorly. All these arteries form a complex vascular system on the lateral surface of the muscle and within its fibres 7.

Venous drainage occurs through the pterygoid plexus and the internal maxillary vein, which lies posterior, superior, and superficial to the buccinator muscle and drains into the buccal vein through the deep facial vein. Anteriorly, the deep facial vein drains into the external (or anterior) facial vein. Sensory innervation occurs through the long buccal nerve, a branch of the maxillary nerve, which runs with the buccal branch of the internal maxillary artery. The motor innervation of the buccinator muscle consists of the temporal and cervical divisions of the facial nerve, which form a plexus near the buccal fat pad. Stensen’s duct also has a critical anatomical relationship with the buccinator muscle, crossing it at the second upper molar.

The buccinator muscle flap can have an anterior, posterior, or superior base depending on the predominant vascularisation 31. The anatomical limits of the flap are the parotid duct superiorly, the oral commissure anteriorly, and the pterygomandibular raphe posteriorly. The lower limit depends on the amount of tissue required, but it is possible to raise a flap up to 7x5 cm 32.

This flap is flexible, versatile, and, unlike most free flaps, provides mucosal rather than exclusively cutaneous coverage. Furthermore, the donor site can be directly closed for defects smaller than 2.5 cm.

Posteriorly based buccinator flap (Bozola)

Bozola et al. 30 first described an axial myo-mucosal flap based posteriorly on the buccal artery. Once the buccal artery has been identified by Doppler ultrasound, the buccal mucosa and the buccinator muscle are incised at the level of the buccopharyngeal fascia and the flap raised in an anteroposterior direction in the loose areolar plane between the buccinator muscle and the buccopharyngeal fascia. The buccopharyngeal fascia is preserved because it prevents herniation of the buccal fat pad and avoids injury to the facial nerve branches. The small branches of the facial artery are ligated, as are the anterior venous tributaries of the pterygoid plexus. The dissection proceeds posteriorly to the pterygomandibular raphe anteriorly, where the main neurovascular bundle enters the flap 30.

A variant of the previously described flap is the posteriorly-based island pedicled buccinator flap, in which the mucosa is incised circumferentially and separated from the adjacent mucosa. However, the flap remains attached to the underlying pedicle, which feeds it via the buccal artery. This modification increases the mobility of the flap. This concept derives from subcutaneous island pedicled skin flaps 33,34.

Buccinator-based myo-mucosal flaps are not suitable for coverage of oral defects larger than 7 cm. Stensen’s duct pierces the buccinator muscle slightly above its centre. Considering a safe distance of 0.5-1 cm from this orifice, only half of the muscle and overlying mucosa can be used for reconstruction. Relocating the Stensen’s duct adds more mucosa, but requires significantly more expertise. Primary donor site closure is possible in defects < 2.5 cm. More significant donor sites defects are managed by mobilising the buccal fat pad, which is progressively re-epithelialised. Other options are represented by skin graft or masseter muscle flap.

However, these flaps are remarkably elastic and malleable and can be stretched to accommodate complex-shaped defects. The arc of rotation of the posteriorly based flaps pedicled on the buccal artery allows reaching the velar, palatine, lateral pharyngeal, and retromolar trigone sites. The buccinator myo-mucosal flap, in its variants, has notable advantages compared to reconstruction with free flaps. It is ideal for surgical units with no experience in microvascular free flaps and fragile patients who cannot tolerate excessively long surgical times 32,33.

Palatal flap

Benign or malignant tumours of the oral cavity, nasal fossa, or paranasal sinuses sometimes require resection of the hard palate to varying degrees. There are different classifications of maxillectomies, mainly based on the extent of resection according to a vertical, horizontal, or transverse orientation 36.

The palatal flap is an axial flap receiving its vascular supply from the greater palatine artery which, emerging from the greater palatine foramen, runs anteriorly to join the nasopalatine vessels at the level of the incisive foramen (Fig. 3) 37.

It provides adequate volume and length with a high success rate due to the robustness of palatal muco-periosteum. This promotes local healing with its own vascular supply and is indicated for the reconstruction of small defects, involving less than one-third of the hard palate with oro-antral fistula, as well as for the reconstruction of partial resections of the soft palate, tonsillar region and medial portion of the retromolar trigone 38-40.

The advantages of the palatal flap are many, including proximity, local availability with minimal donor site morbidity, complete re-epithelisation in 4-6 weeks, little shrinkage, tensile strength with reliable blood supply, preservation of local sensitivity and good mobility. In irradiated patients healing will proceed at a slower pace, taking 6-8 weeks to complete. Limitations are mainly the small size and the limited possibility of axial rotation. The latter is facilitated the greater the length of the flap and if an amount of soft tissue is preserved around the pedicle to increase its torsional strength. Furthermore, by dissecting and skeletonising the greater palatine neurovascular pedicle at its emergence, an additional length of approximately 1 cm can be achieved 41,42. Complications are rare and include haemorrhage and partial or complete necrosis of the flap.

For defects greater than one-third of the palate, the palatal flap can be combined with a buccal inversion flap, and then lifted and inverted to rebuild the mucosa of the nasal floor. The advantage of two-layer closure is the epithelial coverage on both sides of the communication. This is consequently associated to a reduction of flap contraction and risk of infection 39.

In most cases the size of the palatal defects decreases during healing, thanks to its marginal re-epithelisation and temporary prosthetic obturator to close the oro-antral fistula. Therefore, choosing a two-stage closure allows tissue gain and, in selected cases, the possibility of closing even major defects with a palatal flap 39,40.

A disadvantage of the local palatal flap is that it is not applicable in case of defects larger than 50% of the palatal surface. These should therefore be treated by means of obturators or loco-regional or revascularised flaps 43-45.

Bichat’s flap

One of the most effective tools in the reconstruction of intraoral defects is the Bichat‘s fat pad or, as it is commonly known, the buccal fat pad (BFP). First described by Bichat in 1801 as ‘Bichat’s lobule’, the BFP lies in the masticatory space, separating the muscles from each other and acting as a cushion 46,47. It is an anatomically distinct entity characterised by a biconvex, encapsulated shape. The BFP has a central body and four separate processes: buccal, pterygoid, pterygopalatine, and temporal 48,49.

The popularity of BFP as a graft material for closure of intraoral defects, especially oro-antral and oro-nasal fistulas, is mainly due to its ease of access and considerable vascular supply 47,53,54. It is therefore very important to preserve the thin capsule of the flap during harvesting, so as not to damage its delicate blood vessels and compromise its viability 55.

Re-epithelisation of the BFP flap usually occurs within 4 weeks, with excellent functional and aesthetic results 47,53,54. These attributes make it an ideal option for the reconstruction of specific defects, particularly those small to medium-sized, located in the maxilla, extending to the retromolar trigone and palate 55. The size of the defect is crucial in deciding on the use of the BFP. For maxillary defects, the ideal size for such a reconstructive tool should be approximately 4 cm while, for buccal or retromolar defects, it can be up to 6 cm 49-51.

In conclusion, the main advantages of BFP include its ease of harvest and high adaptability with very low morbidity and minimal failure rates. However, its main limitations are that its use is limited to small to medium defects without providing significant volume. Additionally, it is contraindicated in patients with malar hypoplasia 47,56-59.

Nasolabial flap

The nasolabial flap is a widely used flap to reconstruct head defects. The most used approaches are the pedicled subcutaneous nasolabial flap with an upper or lower base, and the pedicled island nasolabial flap on the facial artery and vein (Fig. 4). For the reconstruction of intra-oral defects, a lower-based flap is generally preferred 70.

The skin of the nasolabial fold is supplied from below by multiple branches that arise from the alar branch of the superior labial artery, which in turn arises from the facial artery, and by branches that arrive from the angular artery, which also derives from the facial artery. Laterally, the skin is supplied by the infraorbital artery, a branch of the ophthalmic artery, and by a branch originating from the temporal artery: the transverse facial artery. Thanks to this extensive blood supply, it is possible to design a flap with an inferior or superior base that has as its pedicle the facial or the infraorbital and transverse facial arteries, respectively 71. The skin that can be harvested extends from the medial canthus of the eye to the lower edge of the jaw, and this area is generally hairless if we exclude the lower part of the cheek in men 72. To transpose the flap into the oral cavity, it is necessary to create an access through the buccinator muscle and pass the flap through it. The surgeon can, therefore, decide to transfer the flap in a single-step operation; in this case, it is preferable to de-epithelialise the base of the flap, thus allowing primary closure of the donor region, or to perform the reconstruction in two steps, initially suturing the flap at the intraoral level and, approximately three weeks later, sectioning the pedicle thus allowing complete closure of the donor site 73.

A widespread variant of the nasolabial flap is represented by the island nasolabial flap, which involves the identification of the facial artery and vein and their skeletonisation up to their origin. In this way, the intrinsic problems of the nasolabial flap are overcome, i.e. the presence of a short pedicle that does not allow reaching defects distant from the donor site and the risk of damaging the pedicle in dentate patients. The pedicle in this flap is very long and allows the reconstruction of defects even contralateral to the harvesting site, reaching the recipient site via a tunnel through the oral floor 62.

The nasolabial flap represents a good alternative to reconstruct small and medium-sized intra-oral defects. Different data are reported in the literature: according to some authors, a single nasolabial flap can cover defects of approximately 3 cm, while others repaired defects of up to 5x5 cm 66,74. However, in case of more extensive defects, performing a double nasolabial flap is also possible. The patient of choice for this flap is elderly, where the skin redundancy and laxity allow large flaps to be taken, still allowing a primary closure of the donor region. Moreover, in the edentulous patient the probability of injuring the pedicle is inferior 72. However, the presence of teeth is not an absolute contraindication, as the nasolabial flap can be used in all cases of reconstruction of the buccal mucosa ipsilateral to the harvesting site. In contrast, in cases of reconstruction of the oral floor or tongue, an island nasolabial flap can be used, as previously described 69,73.

As emerges from this analysis, the nasolabial flap is burdened by few serious complications and, in selected cases, can be a valid reconstructive alternative for oral cavity defects.

Biological and synthetic materials and non-reconstruction

In some situations, using flaps to reconstruct the oral cavity may not be possible or may result in over-treatment for minor defects. In such circumstances, one can rely on various materials and strategies. When faced with bone defects in the oral cavity, bone replacement and reconstruction are essential to restore structure and function. Various bone filling and replacement materials are available, although they are not routinely used in surgical practice. Hydroxyapatite and tricalcium phosphate are similar to the mineral component of bone and are used to fill minor bone defects, but are gradually reabsorbed over time. In addition to these, synthetic materials based on ceramics or polymeric resins can be exploited to fill bone spaces and improve the stability of dental prostheses or implants. In case of mucosal or soft tissues defects, specific filling materials are crucial. Some options include the use of synthetic materials such as expanded polytetrafluoroethylene, which can be used to create a mechanical barrier and promote soft tissue regeneration. In the context of future regenerative medicine, laboratory cultivation of epithelial and connective cells will probably create new tissues to routinely reconstruct mucosal defects 75.

Alternatively, other biological materials can also be used, such as bovine pericardium 76 or other biological matrices of bovine collagen 77, which can represent a simple and rapid solution for defects of limited thickness. Another type of material that can be used is a matrix of thrombin and fibrinogen which combines repair with the capacity for haemostasis 78. This matrix can be helpful for small defects and associated with reconstruction by other methods (such as local flaps or primary closure).

The choice of materials is closely related to the size and location of the defect, the patient’s functional and cosmetic needs, as well as the availability of resources and surgical skills. Accurate evaluation of each case is essential to determine the most appropriate strategy. In general, non-reconstruction should be limited to cases in which the defects are small-sized, while the use of synthetic or biological materials to replace the patient’s normal oral mucosa may favour and accelerate the healing process with better functional outcomes.

Proposal for a reconstructive algorithm

Based on the data gathered in our systematic review, we formulated a reconstructive algorithm for minimally-invasive reconstructive options, taking into account the site and size of the defect. Specifically, local options are preferable when defects are not extensive and do not involve multiple tissue types 79, such as bone segments or large muscular volumes (Fig. 5). Furthermore, mucosal defects to be reconstructed by local flaps should have small to medium dimensions, typically not exceeding 20 cm2, although some authors have reported exceptional cases of larger defects successfully reconstructed with these techniques.

This reconstructive approach is ideally suited for patients who do not require neck dissection for oncological reasons, thereby avoiding the associated morbidity linked to neck dissection for isolating vessels needed for vascular anastomosis, as required for microvascular flaps, or creating tunnels for the passage of pedicle in the case of locoregional flaps (e.g., pectoralis major or temporal flaps). It also proves to be a crucial option for patients who are not suitable for lengthy surgeries, such as those necessary for microvascular flap reconstruction.

Careful consideration should be given to the option of non-reconstructing the defect and protecting it with biological materials or allowing healing through secondary intention. This choice is preferable in cases involving a small, predominantly mucosal defect, such as in the genial mucosa or tongue, affecting only the intrinsic musculature, where the risk of salivary fistula or worsening functional outcomes is not anticipated.

Using data extracted from the present analysis, we systematically categorised different flaps based on the type of defect they were employed for. Subsequently, we formulated a proposed decisional algorithm outlining the use of local flaps, structured around the specific defect site (Tab. VII, Fig. 6).

Conclusions

In selected patients with small to moderate-sized defects, the possibility of reconstruction with local flaps can be a viable option. This is particularly true for patients who are not suitable for microvascular surgery and for those in whom neck dissection is not necessary, and in cases where harvesting a flap from a donor site outside the head and neck region would increase morbidity not only at this level but also in the neck, either due to the passage of the pedicle or the preparation of vessels for microvascular anastomoses. Throughout the decision-making process, it is crucial to consider the choice of not reconstructing the defect, opting for healing by secondary intention, or using biological materials for coverage, especially when the defect is solely mucosal and does not entail risks of oro-cutaneous or oro-antral fistulas or predictable functional deficits.

Acknowledgements

The authors would like to thank Michele Barbara for the valuable invitation to participate in and contribute to this work.

Conflict of interest statement

The authors declare no conflict of interest.

Funding

This research did not receive any specific grant from funding agencies in the public, commercial, or not-for-profit sectors.

Author contributions

LC, EF, SB, MA, VD, CA, GN, AN, FZ: conceived the study, collected the data and wrote the paper; RA: corrected the paper; LG: conceived the study and wrote and corrected the paper.

Ethical consideration

The research was conducted ethically, with all study procedures being performed in accordance with the requirements of the World Medical Association’s Declaration of Helsinki.

Figures and tables

Figure 1.PRISMA flow diagram of the review.

Figure 2.Myo-mucosal flap pedicled on the facial artery branches.ECA: external carotid artery; FA: facial artery; IMA: internal maxillary artery; SD: Stensen’s duct.

Figure 3.Palatal flap pedicled on the greater palatine artery.

Figure 4.The nasolabial flap pedicled on the facial artery and vein.

Figure 5.Decisional algorithm for use of minimally-invasive options in oral cavity reconstruction.

Figure 6.Decisional algorithm for use of minimally-invasive options in oral cavity reconstruction.FAMM: facial artery myo-mucosal; t-FAMMIF: tunneled facial artery myo-mucosal island flap; RFAMM: reverse flow FAMM; FAMMIF: facial artery myo-mucosal island flap.

Reconstructive option Number of articles Number of patients
Mucosal/myo-mucosal local flaps
    Based on the facial artery 15 353
    Based on the buccal artery 5 138
    Palatal flap 6 175
Bichat’s flap 8 156
Local skin flaps
    Nasolabial flap 8 500
Total 42 1322
Table I.Number of articles included and study population.
Author Year No. of patients Brief summary Defect site Defect size
Massarelli 13 2023 44 Use of FAMMIF for the reconstruction of defects resulting from malignant tumours of the tongue in cN0 patients yields good functional and QoL outcomes Tongue Medium-sized defects, up to hemiglossectomy
Navarro Cuéllar 14 2021 22 Use of FAMM for the reconstruction of defects resulting from malignant tumours of the tongue and oral floor, simultaneously placing dental implants Tongue and oral floor From 3.7 × 2.1 cm to 6.3 × 4.2 cm
Janardhan 15 2020 16 Comparison between the use of FAMM and nasolabial flaps for reconstructing defects resulting from malignant tumours of the oral cavity. Submucosal oral fibrosis and/or carcinogenesis of the local tissue support the use of the nasolabial flap in the oral cavity Tongue, palate, and oral floor Defects for T1-2 of the tongue, palate, and oral floor
Benjamin 8 2020 21 Use of FAMM for the reconstruction of defects resulting from T1-2 of the tongue and oral floor. Good functional and QoL outcomes. For dentate patients, a bite block was used in the early postoperative days Tongue and oral floor Small and medium-sized defects
Joseph 16 2020 20 Comparison between t-FAMMIF (20 patients) and fascio-cutaneous free flaps (20 patients) in the reconstruction of defects resulting from malignant tumours of the lingual margin Lateral oral tongue Lingual margin lesions not exceeding 4 cm
Massarelli 17 2018 14 t-FAMMIF used for the reconstruction of defects resulting from malignant tumours of the soft palate. Good functional outcomes for both swallowing and speech, as well as for QoL Soft palate Total or subtotal defects of the soft palate
Moro 11 2018 5 t-FAMMIF used in the reconstruction of the lingual margin following excision of malignant tumours. Good reconstructive outcomes Tongue Not specified
Baek 18 2017 19 A pedicled island perforator flap based on the facial artery and veins used for the reconstruction of defects in the tongue, oral floor, and hard palate Tongue, oral floor, and hard palate Medium-sized defects 5.4 × 3.1 cm
Jowett 19 2017 6 Inferiorly pedicled FAMM flap used for malignant tumours of the tongue and oral floor. Good outcomes both aesthetically and in terms of speech articulation. Silicone bite block used during the first postoperative week in dentate patients Tongue and oral floor Medium-sized defects 5.2 x 3.1 cm
Ferrari 12 2016 50 Study on the oncological safety of patients reconstructed with FAMMIF (preservation of facial vessels in cN0) Tongue and oral floor Defects for T1-3 of the tongue and oral floor
van Weert 20 2015 9 Inferiorly based FAMM flap used for defects resulting from T1-2 of the oral floor Oral floor Small to medium-sized defects of the anterior oral floor, including marginal mandibulectomy
O’Leary 21 2011 22 Use of FAMM in various defects for malignant tumours of the oral cavity Oral floor, retromolar trigone, and palate Not specified
Bianchi 22 2009 16 10 FAMM and 6 FAMMIF used for reconstruction of defects resulting from malignant tumours of the oral cavity Tongue, oral floor, and palate Not specified
Ayad 23 2008 57 Inferiorly pedicled FAMM (anterograde flow) used for patients with malignant tumours of the oral floor. Double FAMM used in 4 patients Oral floor 2-3 cm
Joshi 24 2005 12 FAMM used for the reconstruction of defects resulting from the removal of malignant tumours of the oral cavity Oral floor, dental alveoli, and palate Not specified
FAMMIF: facial artery myo-mucosal island flap; t-FAMMIF: tunneled facial artery myo-mucosal island flap; FAMM: facial artery myo-mucosal flap; QoL: quality of life.
Table II.Myo-mucosal flap pedicled on the facial artery.
Author Year No. of patients Brief summary Defect site Defect size
Ferri 25 2020 55 Comparison between patients undergoing pull-through resection and reconstruction with free flap vs patients submitted to transoral resection and reconstruction with buccinator flap. The latter reconstructive option yields superior functional outcomes in terms of tongue motility, Sydney swallowing score, and EORTC QLQ-C30 Tongue and oral floor Not specified
Ahn 26 2017 22 Patients undergoing resections for cT2-3 oral cavity tumours and reconstructed with various types of buccinator flaps. Mean harvesting time was 28.6 minutes, with only one flap necrosis out of 22 cases. Speech and swallowing returned to normal in the postoperative period Oral cavity Mean size 5.3 cm (range, 4-6.7 cm) in length and 3.8 cm (range, 2-5 cm) in width.
Bardazzi 27 2017 27 Posteriorly-based buccinator flap for reconstruction of tongue defects, covering the donor site with buccal fat. Satisfactory functional outcomes Tongue Not specified
Ferrari 28 2012 19 Use of Bozola flap for reconstruction of the palate, cheek, posterolateral region of the tongue, and oral floor. It resulted in patients fully regaining their swallowing capacity and speech after reconstruction Hard palate, cheek, oral floor Mean 4 cm
Ferrari 29 2011 15 Assessment of complications at the donor site in case of island myo-mucosal flap from the buccinator muscle. Evaluation based on mouth opening, symmetry of the oral commissure, restoration of the inner vestibule, mucosal coverage of the cheek, and aesthetics. It was demonstrated that for moderate-sized defects of the tongue and oral floor, donor site complications are negligible since it can be primarily closed for defects smaller than 2.5 cm Tongue and oral floor Not specified
Table III.Myo-mucosal flap based on the buccal artery.
Author Year No. of patients Brief summary Defect site Defect size
Jung 39 2013 5 Delayed closure of the palatal defect using buccal inversion and palatal rotation flaps after maxillectomy Hard palate Not specified
Salins 38 2009 53 Reconstruction of the retromolar region Retromolar region Not specified
Anavi 37 2003 63 Palatal rotation-advancement flap for delayed repair of oro-antral fistula Hard palate 2.3-1.6 cm
Lee 40 2002 21 Repair of oro-antral communication in molar region by random palatal flap Hard palate Not specified
Ducic 40 2001 28 Reconstruction with palatal flaps in conjunction with microvascular free tissue transfer Complex oro-mandibular defects Not specified
Genden 41 2001 5 Palatal island flap for reconstruction of palatal and retromolar trigone Hard palate and retromolar region Not specified
Table IV.Palatal flap.
Author Year No. of patients Brief summary Defect site Defect size
Chaudhary 51 2014 15 Use of the Bichat’s flap for maxillary reconstruction Hard palate, alveolar crest 2-5 cm
Toshihiro 54 2013 23 Description of the technique, advantages and results for reconstruction of the oral cavity after oncological resection Oral cavity 1.5-3 cm
Colella 60 2004 15 Description of the technique, advantages and results for reconstruction of the oral cavity after oncologic resection Oral cavity 2-4x5 cm
Zhong 61 2004 38 (3 < 16 yo) Use of the Bichat’s flap for bone graft coverage after maxillectomy Hard palate Not specified
Dean 59 2000 32 Description of the technique, advantages and results for reconstruction of the oral cavity after oncologic resection Oral cavity and lateral wall of the oropharynx 4 cm
Baumann 52 2000 12 Use of the Bichat’s flap for reconstruction of the hard palate Hard palate 5.5-4 cm
Table V.Bichat’s flap.
Author Year No. of patients Brief summary Defect site Defect size
Sharma 62 2021 11 Reconstruction with island nasolabial flap following resection of T2-3 of the tongue Tongue 7 cm greater extension
Shetty 63 2020 128 Reconstruction after resection of T1-3 cancer of the oral cavity. Evaluation of QoL (University of Washington QoL Questionnaire), objective evaluation of buccal opening and nasolabial scar (Vancouver scar scale). Useful flap for the reconstruction of small and medium-sized oral defects, with good QoL, significant improvement in mouth opening, and acceptable aesthetic results 38 buccal mucosa, 15 oral commissure, 9 upper gum, 64 lower gum and retromolar trigone, 1 palate Not specified
Lazaridou 69 2016 49 Comparison between patients with pedicled nasolabial and nasolabial island flaps in the reconstruction of oral cavity defects after carcinoma in terms of complications, sensitivity, and quality of life. The island flap has shown a higher rate of complications, as well as a reduced quality of life due to dental problems. Recovery of tactile sensation of the flap was incomplete in approximately half of patients 29 oral floor, 4 tongue, 11 gum, 5 buccal mucosa Not specified
Alonso-Rodriguez 64 2014 16 Reconstruction of oral cavity defects after resection of T1-4a carcinomas of the oral cavity. Good functional and aesthetic results. Complications: 2 wound dehiscences, 2 haematomas, 1 oro-cutaneous fistula 5 tongue, 8 upper and lower gum, 3 oral floor 5 cm
El-Marakby 65 2012 20 Reconstruction of defects after resection of T1-2 carcinomas of the oral cavity. 90% of patients were satisfied with aesthetic results, 70% of patients were satisfied with functional result (chewing, speaking, swallowing). Complications: 1 haemorrhage, 1 ectropion, 1 wound dehiscence Oral floor, buccal mucosa 2-4.5 cm
Singh 68 2012 26 Patients affected by T2-3 N0-1 carcinomas of the oral cavity. Good functional and aesthetic results. In some patients the facial artery was ligated during neck dissection, without flap necrosis. Three patients had wound dehiscences, 1 oro-cutaneous fistula, and 1 wound infection 11 buccal mucosa, 4 gum, 4 tongue, 4 oral commissure Not specified
Maurer 66 2002 26 Reconstruction after T1-2 resection of the oral cavity. Satisfactory functional and aesthetic results for all patients. In 19 patients it was possible to relocate the dental prosthesis Oral floor, buccal mucosa Not specified
Varghese 67 2001 224 Reconstruction after resection of T1-4 oral cavity cancers. In 211 patients a two-step, while in 13 edentulous patients a one-step reconstruction were accomplished. All patients recovered swallowing for both solids and liquids. Among 182 patients with lip reconstruction, 135 had good, 42 intelligible, and 5 unintelligible speech. All these 5 patients had undergone subtotal glossectomy with total or partial flap loss. Complications: total flap necrosis in 15 patients and partial flap necrosis in 13 patients Oral cavity 6 cm
Table VI.Nasolabial flap.
Defect site Possible options
Oral tongue FAMM t-FAMMIF Nasolabial
Floor of the mouth FAMM t-FAMMIF Nasolabial
Buccal mucosa Bichat Nasolabial
Soft palate FAMM Buccinator Palatal
Hard palate RFAMM Buccinator Palatal Bichat Nasolabial
Retromolar trigone FAMM Buccinator Palatal Bichat Nasolabial
Superior lip RFAMM Nasolabial
Inferior lip FAMM Nasolabial
Oropharynx (tonsil) FAMMIF Buccinator Palatal
FAMM: facial artery myo-mucosal; t-FAMMIF: tunneled facial artery myo-mucosal island flap; RFAMM: reverse flow FAMM; FAMMIF: facial artery myo-mucosal island flap.
Table VII.Recipient sites and corresponding local flaps.

References

  1. Ettinger KS, Ganry L, Fernandes RP. Oral cavity cancer. Oral Maxillofac Surg Clin North Am. 2019; 31:13-29. DOI
  2. Gazzini L, Fazio E, Dallari V. Impact of the COVID-19 pandemic on head and neck cancer diagnosis: data from a single referral center, South Tyrol, northern Italy. Eur Arch Otorhinolaryngol. 2022; 279:3159-3166. DOI
  3. Pipkorn P, Rosenquist K, Zenga J.. Functional considerations in oral cavity reconstruction. Curr Opin Otolaryngol Head Neck Surg. 2018; 26:326-333. DOI
  4. Quadri P, McMullen C.. Oral cavity reconstruction. Otolaryngol Clin North Am. 2023; 56:671-686. DOI
  5. Chuanjun C, Zhiyuan Z, Shaopu G. Speech after partial glossectomy: a comparison between reconstruction and nonreconstruction patients. J Oral Maxillofac Surg. 2002; 60:404-407. DOI
  6. Pribaz J, Stephens W, Crespo L. A new intraoral flap: facial artery musculomucosal (FAMM) flap. Plast Reconstr Surg. 1992; 90:421-429. DOI
  7. Zhao Z, Li S, Yan Y. New buccinator myomucosal island flap: anatomic study and clinical application. Plast Reconstr Surg. 1999; 104:55-64.
  8. Benjamin M, Aliano K, Davenport T. Functional outcomes regarding facial artery musculomucosal flap for reconstruction of partial glossectomy defects. Ann Plast Surg. 2020; 85:S76-S79. DOI
  9. Massarelli O, Vaira LA, Biglio A. Rational and simplified nomenclature for buccinator myomucosal flaps. Oral Maxillofac Surg. 2017; 21:453-459. DOI
  10. Copelli C, Manfuso A, Di Maio P. Myomucosal island flap in the reconstruction of oral cavity defects: description of the surgical technique. Head Neck. 2023; 45:745-751. DOI
  11. Moro A, Saponaro G, Doneddu P. The arterialized facial artery musculo-mucosal island flap for post-oncological tongue reconstruction. J Craniofac Surg. 2018; 29:2021-2025. DOI
  12. Ferrari S, Ferri A, Bianchi B. Oncologic safety of facial artery myomucosal flaps in oral cavity reconstruction. Head Neck. 2016; 38:E1200-E1202. DOI
  13. Massarelli O, Vaira LA, Crimi S. Tongue reconstruction with buccinator myomucosal island flaps: technical considerations, oncologic safety, functional outcomes and QoL assessment. A retrospective observational study. J Pers Med. 2023; 13:879-885. DOI
  14. Navarro Cuéllar C, Tousidonis Rial M, Antúnez-Conde R. Functional outcomes with facial artery musculo-mucosal (FAMM) flap and dental implants for reconstruction of floor of the mouth and tongue defects in oncologic patients. J Clin Med. 2021; 10:3625-3630. DOI
  15. Janardhan D, George CK, Thomas S. Island NLF or island FAMM flap in reconstruction of oral malignancy defects?. Indian J Surg Oncol. 2020; 11:188-191. DOI
  16. Joseph ST, Mohan MT, Tharayil J.. Comparison of islanded facial artery myomucosal flap with fasciocutaneous free flaps in the reconstruction of lateral oral tongue defects. Int J Oral Maxillofac Surg. 2020; 49:1000-1006. DOI
  17. Massarelli O, Vaira LA, Gobbi R. Soft palate functional reconstruction with buccinator myomucosal island flaps. Int J Oral Maxillofac Surg. 2018; 47:316-323. DOI
  18. Baek CH, Kim BY, Park WR. Modification of facial artery myomucosal flap: a novel perforator flap for upper aerodigestive tract reconstruction after head and neck cancer ablation. Clin Otolaryngol. 2017; 42:880-885. DOI
  19. Jowett N, Hadlock TA, Sela E. Facial mimetic, cosmetic, and functional standardized assessment of the facial artery musculomucosal (FAMM) flap. Auris Nasus Larynx. 2017; 44:220-226. DOI
  20. van Weert S, Leemans CR. The facial artery musculomucosal flap revisited. Surgical technique and critical functional appraisal: our experience in nine patients. Clin Otolaryngol. 2015; 40:48-52. DOI
  21. O’Leary P, Bundgaard T.. Good results in patients with defects after intraoral tumour excision using facial artery musculo-mucosal flap. Dan Med Bull. 2011; 58:A4264.
  22. Bianchi B, Ferri A, Ferrari S. Myomucosal cheek flaps: applications in intraoral reconstruction using three different techniques. Oral Surg Oral Med Oral Pathol Oral Radiol Endod. 2009; 108:353-359. DOI
  23. Ayad T, Kolb F, De Monés E. Reconstruction of floor of mouth defects by the facial artery musculo-mucosal flap following cancer ablation. Head Neck. 2008; 30:437-445. DOI
  24. Joshi A, Rajendraprasad JS, Shetty K.. Reconstruction of intraoral defects using facial artery musculomucosal flap. Br J Plast Surg. 2005; 58:1061-1066. DOI
  25. Ferri A, Perlangeli G, Montalto N. Transoral resection with buccinator flap reconstruction vs. pull-through resection and free flap reconstruction for the management of T1/T2 cancer of the tongue and floor of the mouth. J Craniomaxillofac Surg. 2020; 48:514-520. DOI
  26. Ahn D, Lee GJ, Sohn JH. Reconstruction of oral cavity defect using versatile buccinator myomucosal flaps in the treatment of cT2-3, N0 oral cavity squamous cell carcinoma: feasibility, morbidity, and functional/oncological outcomes. Oral Oncol. 2017; 75:95-99. DOI
  27. Bardazzi A, Beltramini GA, Autelitano L. Use of buccinator myomucosal flap in tongue reconstruction. J Craniofac Surg. 2017; 28:1084-1087. DOI
  28. Ferrari S, Copelli C, Bianchi B. The Bozola flap in oral cavity reconstruction. Oral Oncol. 2012; 48:379-82. DOI
  29. Ferrari S, Ferri A, Bianchi B. Donor site morbidity using the buccinator myomucosal island flap. Oral Surg Oral Med Oral Pathol Oral Radiol Endod. 2011; 111:306-11. DOI
  30. Bozola AR, Gasques JA, Carriquiry CE. The buccinator musculomucosal flap: anatomic study and clinical application. Plast Reconstr Surg. 1989; 84:250-257. DOI
  31. Tezel E. Buccal mucosal flaps: a review. Plast Reconstr Surg. 2002; 109:735-741. DOI
  32. Carstens MH, Stofman GM, Hurwitz DJ. The buccinator myomucosal island pedicle flap: anatomic study and case report. Plast Reconstr Surg. 1991; 88:39-50.
  33. Kimyai-Asadi A, Goldberg LH. Island pedicle flap. Dermatol Clin. 2005; 23:113-127. DOI
  34. Nakajima T, Yoshimura Y, Kami T.. The subcutaneous pedicle flap: widening of its applications. Ann Plast Surg. 1987; 19:103-116. DOI
  35. Van Lierop AC, Fagan JJ. Buccinator myomucosal flap: clinical results and review of anatomy, surgical technique and applications. J Laryngol Otol. 2008; 122:181-187. DOI
  36. Bidra AS, Jacob RF, Taylor TD. Classification of maxillectomy defects: a systematic review and criteria necessary for a universal description. J Prosthet Dent. 2012; 107:261-270. DOI
  37. Anavi Y, Gal G, Silfen R. Palatal rotation-advancement flap for delayed repair of oroantral fistula: a retrospective evaluation of 63 cases. Oral Surg Oral Med Oral Pathol Oral Radiol Endod. 2003; 96:527-534. DOI
  38. Salins PC, Benjamin P.. Anatomic basis for reconstitution of retromolar region: significance of palatal flap. J Oral Maxillofac Surg. 2009; 67:1141-1148. DOI
  39. Jung S, Kook MS, Park HJ. Delayed closure of the palatal defect using buccal inversion and palatal rotation flaps after maxillectomy. J Craniofac Surg. 2013; 24:660-664. DOI
  40. Lee JJ, Kok SH, Chang HH. Repair of oroantral communications in the third molar region by random palatal flap. Int J Oral Maxillofac Surg. 2002; 31:677-680. DOI
  41. Genden EM, Lee BB, Urken ML. The palatal island flap for reconstruction of palatal and retromolar trigone defects revisited. Arch Otolaryngol Head Neck Surg. 2001; 127:837-841.
  42. Ducic Y, Herford AS. The use of palatal island flaps as an adjunct to microvascular free tissue transfer for reconstruction of complex oromandibular defects. Laryngoscope. 2001; 111:1666-1669. DOI
  43. Sakuraba M, Kimata Y, Ota Y. Simple maxillary reconstruction using free tissue transfer and prostheses. Plast Reconstr Surg. 2003; 111:594-600. DOI
  44. Dalgorf D, Higgins K.. Reconstruction of the midface and maxilla. Curr Opin Otolaryngol Head Neck Surg. 2008; 16:303-311. DOI
  45. Pandolfi PJ, Yavuzer R, Jackson IT. Three-layer closure of an oroantral-cutaneous defect. Int J Oral Maxillofac Surg. 2000; 29:24-26. DOI
  46. Samman N, Cheung LK, Tideman H.. The buccal fat pad in oral reconstruction. Int J Oral Maxillofac Surg. 1993; 22:2-6. DOI
  47. Rapidis AD, Alexandridis CA, Eleftheriadis E. The use of the buccal fat pad for reconstruction of oral defects: review of the literature and report of 15 cases. J Oral Maxillofac Surg. 2000; 58:158-163. DOI
  48. Zhang HM, Yan YP, Qi KM. Anatomical structure of the buccal fat pad and its clinical adaptations. Plast Reconstr Surg. 2002; 109:2509-2520. DOI
  49. Tideman H, Bosanquet A, Scott J.. Use of the buccal fat pad as a pedicled graft. J Oral Maxillofac Surg. 1986; 44:435-440. DOI
  50. Neder A. Use of buccal fat pad for grafts. Oral Surg Oral Med Oral Pathol. 1983; 55:349-350. DOI
  51. Chaudhary B, Gong Z, Lin Z. Reconstruction of intraoral maxillary defect with buccal fat pad. J Craniofac Surg. 2014; 25:2174-2177. DOI
  52. Baumann A, Ewers R.. Application of the buccal fat pad in oral reconstruction. J Oral Maxillofac Surg. 2000; 58:389-393. DOI
  53. el-Hakim IE, el-Fakharany AM. The use of the pedicled buccal fat pad (BFP) and palatal rotating flaps in closure of oroantral communication and palatal defects. J Laryngol Otol. 1999; 113:834-838. DOI
  54. Toshihiro Y, Nariai Y, Takamura Y. Applicability of buccal fat pad grafting for oral reconstruction. Int J Oral Maxillofac Surg. 2013; 42:604-610. DOI
  55. Hao SP. Reconstruction of oral defects with the pedicled buccal fat pad flap. Otolaryngol Head Neck Surg. 2000; 122:863-867. DOI
  56. Tostevin PM, Ellis H.. The buccal pad of fat: a review. Clin Anat. 1995; 8:403-406. DOI
  57. Katre MI, Deshmukh SD, Dhanajkar PS. Buccal fat pad: a forgotten option of reconstruction in oral cancer. Indian J Otolaryngol Head Neck Surg. 2019; 71:248-252. DOI
  58. Stuzin JM, Wagstrom L, Kawamoto HK. The anatomy and clinical applications of the buccal fat pad. Plast Reconstr Surg. 1990; 85:29-37. DOI
  59. Dean A, Alamillos F, Garcia-Lopez A. The buccal fat pad flap in oral reconstruction. Head Neck. 2001; 23:383-388. DOI
  60. Colella G, Tartaro G, Giudice A.. The buccal fat pad in oral reconstruction. Br J Plast Surg. 2004; 57:326-329. DOI
  61. Zhong LP, Chen GF, Fan LJ. Immediate reconstruction of maxilla with bone grafts supported by pedicled buccal fat pad graft. Oral Surg Oral Med Oral Pathol Oral Radiol Endod. 2004; 97:147-154. DOI
  62. Sharma V, Pandey S, Gandhi AK. Island nasolabial flap for tongue reconstruction: locoregional flap of choice and an alternative to free flap for tongue cancer. Indian J Surg Oncol. 2021; 12:94-99. DOI
  63. Shetty RK, Pradhan S, Kannan R. Clinical profile and quality of life assessment of oral cancer patients following nasolabial flap reconstruction surgery. Indian J Otolaryngol Head Neck Surg. 2020; 72:200-207. DOI
  64. Alonso-Rodríguez E, Cebrián-Carretero JL, Morán-Soto MJ. Versatility of nasolabial flaps in oral cavity reconstructions. Med Oral Patol Oral Cir Bucal. 2014; 19:E525-E530. DOI
  65. El-Marakby HH, Fouad FA, Ali AH. One stage reconstruction of the floor of the mouth with a subcutaneous pedicled nasolabial flap. J Egypt Natl Canc Inst. 2012; 24:71-76. DOI
  66. Maurer P, Eckert AW, Schubert J.. Functional rehabilitation following resection of the floor of the mouth: the nasolabial flap revisited. J Craniomaxillofac Surg. 2002; 30:369-372. DOI
  67. Varghese BT, Sebastian P, Cherian T. Nasolabial flaps in oral reconstruction: an analysis of 224 cases. Br J Plast Surg. 2001; 54:499-503. DOI
  68. Singh S, Singh RK, Pandey M.. Nasolabial flap reconstruction in oral cancer. World J Surg Oncol. 2012; 10:227-230. DOI
  69. Maria L, Ioannis D, Konstantinos V. Histological changes in nasolabial cutaneous flaps employed in intraoral reconstruction. J Maxillofac Oral Surg. 2017; 16:292-299. DOI
  70. Ducic Y, Burye M.. Nasolabial flap reconstruction of oral cavity defects: a report of 18 cases. J Oral Maxillofac Surg. 2000; 58:1104-1109. DOI
  71. Cormack GC, Lamberty BGH. The arterial anatomy of skin flaps. Churchill Livingstone: Edinburgh; 1994.
  72. Kallappa S, Shah N.. Outcome of nasolabial flap in the reconstruction of head and neck defects. Indian J Surg Oncol. 2019; 10:577-581. DOI
  73. Fernandes R. Local and regional flaps in head and neck reconstruction: a practical approach. John Wiley &amp; Sons: New York, NY; 2015. DOI
  74. Eckardt AM, Kokemüller H, Tavassol F. Reconstruction of oral mucosal defects using the nasolabial flap: clinical experience with 22 patients. Head Neck Oncol. 2011; 3:28-34. DOI
  75. Toledano M, Toledano-Osorio M, Carrasco-Carmona Á. State of the art on biomaterials for soft tissue augmentation in the oral cavity. Part II: synthetic polymers-based biomaterials. Polymers (Basel). 2020; 12:1845-1850. DOI
  76. Tirelli G, Tofanelli M, Piccinato A. An alternative to skin graft for superficial surgical defect in oral cancer surgery. Braz J Otorhinolaryngol. 2021; 87:678-682. DOI
  77. Srivastava A, Maniakas A, Myers J. Reconstruction of intraoral oncologic surgical defects with Integra® bilayer wound matrix. Clin Case Rep. 2020; 9:213-219. DOI
  78. Cuesta-González FJ, Arranz-Obispo CD, Pozuelo-Arquimbau L. Functional outcomes after glossectomies: pilot study on use of a thrombin-fibrinogen biosponge (TachoSil). Oral Surg Oral Med Oral Pathol Oral Radiol. 2019; 127:24-29. DOI
  79. Gazzini L, Fazio E, Dallari V. Beyond the boundaries of compartmental hemiglossectomy: a proposal for an anatomically based classification of surgical approaches to advanced oral tongue squamous cell carcinoma. Eur Arch Otorhinolaryngol. 2023; 280:3015-3022. DOI

Affiliations

Luca Calabrese

Department of Otolaryngology-Head and Neck Surgery, Hospital of Bolzano (SABES-ASDAA), Teaching Hospital of the Paracelsus Medical Private University (PMU), Bolzano, Italy

Enrico Fazio

Department of Otolaryngology-Head and Neck Surgery, Hospital of Bolzano (SABES-ASDAA), Teaching Hospital of the Paracelsus Medical Private University (PMU), Bolzano, Italy

Sara Bassani

Department of Otolaryngology-Head and Neck Surgery, University Hospital of Verona, Verona, Italy

Monir Abousiam

Department of Otolaryngology-Head and Neck Surgery, Hospital of Bolzano (SABES-ASDAA), Teaching Hospital of the Paracelsus Medical Private University (PMU), Bolzano, Italy

Virginia Dallari

Department of Otolaryngology-Head and Neck Surgery, University Hospital of Verona, Verona, Italy. Corresponding author - virginia.dallari@gmail.com

Cecilia Albi

Department of Otolaryngology-Head and Neck Surgery, University Hospital of Ferrara, Ferrara, Italy

Giuseppe Nucera

Department of Otolaryngology-Head and Neck Surgery, Hospital of Bolzano (SABES-ASDAA), Teaching Hospital of the Paracelsus Medical Private University (PMU), Bolzano, Italy

Aurel Nebiaj

Department of Otolaryngology-Head and Neck Surgery, Hospital of Bolzano (SABES-ASDAA), Teaching Hospital of the Paracelsus Medical Private University (PMU), Bolzano, Italy

Francesca Zanghi

Department of Otolaryngology-Head and Neck Surgery, Hospital of Bolzano (SABES-ASDAA), Teaching Hospital of the Paracelsus Medical Private University (PMU), Bolzano, Italy

Remo Accorona

Department of Otolaryngology-Head and Neck Surgery, Niguarda Hospital, Milan, Italy

Luca Gazzini

Department of Otolaryngology-Head and Neck Surgery, Hospital of Bolzano (SABES-ASDAA), Teaching Hospital of the Paracelsus Medical Private University (PMU), Bolzano, Italy

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© Società Italiana di Otorinolaringoiatria e chirurgia cervico facciale , 2024

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