Journal of Cutaneous and Aesthetic Surgery

SHORT COMMUNICATION
Year
: 2020  |  Volume : 13  |  Issue : 4  |  Page : 353--356

Surgical management of oral mucocele: Experience with marsupialization


Chander Grover 
 Department of Dermatology & STD, University College of Medical Sciences & GTB Hospital, New Delhi, India

Correspondence Address:
Chander Grover
Department of Dermatology and STD, UCMS and GTB Hospital, Dilshad Garden, Delhi-110095.
India

Abstract

Oral mucoceles are a common and nagging problem. They are proposed to be a result of damage to the minor salivary gland structure, resulting in retention or extravasation of saliva which leads to these cystic lesions. The lesions may often resolve spontaneously but frequently recur, or even epithelialize over long periods of time. This study reports the results of surgical management of oral mucocele by marsupialization. Even though, a complete surgical removal is considered the treatment of choice for oral mucocele, it has associated disadvantages including a longer recovery period and potential for ductal damage, which can lead to scarring, recurrence, and development of further satellite lesions. As the study shows, marsupialization is a simple surgery which ensures faster healing, minimizes postoperative complications, and is associated with a minimal risk of recurrence or development of new lesions. Owing to the satisfactory response to marsupialization, it may be considered as first line therapy in the management of oral mucoceles.



How to cite this article:
Grover C. Surgical management of oral mucocele: Experience with marsupialization.J Cutan Aesthet Surg 2020;13:353-356


How to cite this URL:
Grover C. Surgical management of oral mucocele: Experience with marsupialization. J Cutan Aesthet Surg [serial online] 2020 [cited 2022 Jun 25 ];13:353-356
Available from: https://www.jcasonline.com/text.asp?2020/13/4/353/301493


Full Text



A mucocele is a glandular collection, commonly arising from the salivary glands, but it is also reported in other locations such as the lacrimal sac, paranasal sinuses, etc. The oral mucocele is a common lesion, seen in 0.4–0.9% of the general population. It is characterized by a rapid appearance, specific location, history of trauma, bluish color, and cystic consistency.[1] Almost 70% lesions arise in the lower labial mucosa.[2] Though asymptomatic, treatment is often requested due to the size of the lesions. We have been treating these lesions with the simple technique of marsupialization for the past 5 years, with good results.

Data from a total of 13 patients with 17 oral mucoceles treated over the past 5 years were retrospectively analyzed. There were eight males and five females in this group (M:F ratio being 1.6:1). The mean age at presentation was 17.9 years (range 8–30 yrs). Nine patients presented with a single large lesion causing discomfort, whereas four patients had two or more lesions requiring intervention. Of these, two patients had numerous lesions that were visualized better on magnification [Figure 1] and [Figure 2]. The lesion of interest was present in the labial mucosa [Figure 1] and [Figure 2] (15/17 or 88.2%) or buccal mucosa [Figure 3] (2/17 or 11.8%) cases. The average size of the lesion was 13.2 mm (range 5–25 mm). The majority of the lesions presented as a translucent cystic nodule [Figure 1] and [Figure 2] (6/17 or 35%), a bluish translucent cyst [Figure 4] (6/17 or 35%), or whitish papule or tag-like appearance [Figure 2] (5/17 or 29.3%) cases.{Figure 1} {Figure 2} {Figure 3} {Figure 4}

All the patients were treated with marsupialization. The area was cleaned with povidone iodine, with the patient clenching a piece of sterile gauze between his teeth. Local anesthesia, a combination of 2% lignocaine with adrenaline, was given [Figure 5]A. A chalazion clamp was then used to encircle and hold the mucocele [Figure 5]B. It helped by making the lesions prominent, provided grip over slippery mucosa, and also minimized bleeding. A cruciate incision (two incisions perpendicular to each other) was given over the most prominent part of the lesion [Figure 5]C, [D]. The incisions were deep enough to reach the cyst cavity, discharging the mucoid contents that were cleaned and emptied. Subsequently, the four triangular flaps of the cyst roof were snipped with a sharp scissors to de-roof the cavity [Figure 5]E, making the floor of the cyst a part of the oral mucosa. This formed a continuous surface from the exterior to the interior of the cyst [Figure 5]F. No sutures were applied, and hemostasis was secured with pressure or with a gauze soaked in adrenaline. The chalazion clamp was relieved, and the site was packed for 10–15 min to ensure there was no ongoing bleeding. The patient was prescribed antiseptic gargles for a week and nonsteroidal anti-inflammatory drug for 3–4 days. Softer diet was advised for the first 2–3 days, and patients were reviewed at 1 week to assess resolution and complete healing in all cases [Figure 6]A, [B]. Recurrence was observed in 2 out of 17 cases (11.7%), at 2–3 weeks, which was treated with a repeat of the same procedure by using a deeper incision, leading to complete resolution.{Figure 5} {Figure 6}

Oral mucocele is the most common benign lesion of the oral cavity,[3] frequently arising in the 2nd to 3rd decade, though it may occasionally be present at birth. Mucoceles are a result of traumatization (extravasation mucocele) or blockage of the salivary gland duct (retention mucocele).[1] Various acquired causes include trauma (lip/ cheek biting, piercing), mucosal inflammation, immunological reaction, chronic inflammation, infection, and duct obstruction due to sialolith or dense mucosa. Multiple lesions are generally a result of oral mucosal inflammation associated with Sjogren’s syndrome, sarcoidosis, HIV, lichen planus, lichenoid drug reaction, and chronic graft-versus-host disease. Some reports have implicated the use of tartar-control toothpastes, or even neoplasia. Advanced or larger lesions may be associated with granuloma or pseudo-capsule formation.

Clinically, the most common site of presentation is the lower lip, as was seen in our series.[3] The lesions are usually asymptomatic, with most of our patients presenting only with an awareness of a swelling or mild discomfort. Color variation depends on the size and surface proximity of the lesion. Superficial lesions tend to be bluish, whereas deeper lesions may have a mucosal color. The same was corroborated in our findings. Patients with white, keratotic papules were the ones with a longer standing history.

Mucoceles may resolve spontaneously, and this history was given by a majority of our patients, who, however, experienced a recurrence after varying periods. Superficial mucoceles are likely to recur periodically, with new lesions developing over time. This history is especially useful for ruling out differential diagnoses such as fibroma, lipoma, sialolith, phlebolith, salivary gland neoplasms, etc. Diagnosis can also be confirmed by simple aspiration or fine needle aspiration cytology (FNAC).

Various treatment modalities described in the literature include intralesional steroids (betamethasone or dexamethasone), sclerotherapy, ablation, or surgical removal.[5] Ablative therapy with laser or cryosurgery is useful for multiple lesions.[4] However, surgical removal is the most definitive and most commonly used treatment. We opted for conservative surgery, that is, marsupialization as compared with surgical excision (treatment of choice but with a longer downtime and more scarring),[5] or micro-marsupialization (involves retained sutures in the oral cavity for a week).[6] Marsupialization is useful for cysts where single draining may not be effective; at the same time, complete removal of surrounding structures is not desirable. It is well described for Gartner’s duct cyst, Bartholin’s cyst, pancreatic cysts, pilonidal cysts, dacryocystorhinostomy, or endoscopy. However, literature on oral mucoceles is limited. In oral mucoceles, suturing of edges is also not required as lesions are often small, and pressure hemostasis is achievable. Other advantages include lesser chances of recurrence, faster healing as not much epithelialization is required,[7] lesser risk of secondary infection as lesser raw surface is exposed, and the ability to deal with larger lesions without much collateral damage.[8]

Postoperative advice is similar to other mucosal surgeries, such as a soft- or liquid-based, bland diet and strict avoidance of hot beverages and tobacco. However, the extent of dietary modification required was quite minimal, with most patients resuming a normal diet by the 3rd to 4th day. For patients with multiple lesions, preventive advice includes avoidance of trauma, habits that irritate minor salivary glands (sucking, chewing on lips or tongue etc.), restoration of damaged teeth or orthodontic appliances, wearing mouthguards during contact sports, treating mucosal disease, and managing xerostomia. Potential complications include bleeding, damage to peripheral nerves, injury to Wharton’s duct, stenosis, obstructive sialadenitis, saliva leakage, injury to lingual nerve, temporary/ permanent paresthesia, postoperative hematoma, infection, or wound dehiscence. Fortunately, these are associated with more extensive surgery and did not occur in any of our cases.

To conclude, marsupialization is an effective surgical treatment for oral mucoceles requiring treatment. It is associated with lesser downtime, minimal adverse effects, and higher treatment success rates.

Declaration of patient consent

The authors certify that they have obtained all appropriate patient consent forms. In the form/forms, the patient(s) has/have given his/her/their consent for his/her/their images and other clinical information to be reported in the journal. The patients understand that their names and initials will not be published and due efforts will be made to conceal their identity, but anonymity cannot be guaranteed.

Financial support and sponsorship

Nil.

Conflicts of interest

There are no conflicts of interest.

References

1Ata-Ali J, Carrillo C, Bonet C, Balaguer J, Peñarrocha M, Peñarrocha M Oral mucocele: Review of the literature. J Clin Exp Dent 2010;2:e18-21.
2Suryavanshi R, Abdullah A, Singh N, Astekar M Oral mucocele in infant with an unusual presentation. BMJ Case Rep 2020;13:e234669.
3Błochowiak K, Farynowska J, Sokalski J, Wyganowska-Świątkowska M, Witmanowski H Benign tumours and tumour-like lesions in the oral cavity: A retrospective analysis. Postepy Dermatol Alergol 2019;36:744-51.
4De Falco D, Di Venere D, Maiorano E Diode laser excision of Blandin-Nuhn mucocele. Cureus 2020;12:e7441.
5Sinha R, Sarkar S, Khaitan T, Kabiraj A, Maji A Nonsurgical management of oral mucocele by intralesional corticosteroid therapy. Int J Dent2016;2016:2896748. doi: 10.1155/2016/2896748.
6Delbem AC, Cunha RF, Vieira AE, Ribeiro LL Treatment of mucus retention phenomena in children by the micro-marsupialization technique: Case reports. Pediatr Dent 2000;22:155-8.
7Morita Y, Sato K, Kawana M, Takahasi S, Ikarashi F Treatment of ranula—excision of the sublingual gland versus marsupialization. Auris Nasus Larynx 2003;30:311-4.
8Baurmash HD Marsupialization for treatment of oral ranula: A second look at the procedure. Journal of Oral and Maxillofacial Surgery 1992;50:1274-9.