Case Report
DOI: http://dx.doi.org/10.18203/issn.2454-5929.ijohns20160965
Mucocele of the nasal septum post inferior turbunectomy
Department of Otorhinolaryngology, OHUD Hospital, Madinah, Saudi Arabia
Received: 22 February 2016
Accepted: 27 March 2016
*Correspondence:
Dr. Roa Talal Halawani,
E-mail: Roa_halawani@yahoo.com
Copyright: © the author(s), publisher and licensee Medip Academy. This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial License, which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
ABSTRACT
Paranasal mucocele is a benign cystic lesion. Mostly in the fronto-ethmoidal sinuses. Mucocele of the nasal septum is extremely rare. We report a septum mucocele in a 20-year-old male presenting with bilateral nasal obstruction occurred after inferior turbunectomy. Clinical and radiological features are presented and discussed.
Keywords: Mucocele, Nasal Septum, Inferior turbunectomy
INTRODUCTION
Paranasal sinuses mucoceles are benign, expansile cystic masses covered by respiratory epithelium, resulting from accumulation and retention of mucus secretion. These lesions are thought to be secondary to an obstruction of the sinus ostium caused by an inflammation, trauma, fibrosis or previous surgery.1 Symptoms of the paranasal sinus mucoceles may vary depending on the size and location of the mucocele. Mucocele of the nasal septum is extremely rare and first reported in 2002 by Gall and Witterick and 6 cases have been reported so far in the literature.2-5,7
CASE REPORT
A 20-year-old male patient visited our outpatient clinic complaining of bilateral nasal obstruction, rhinorrhea and nasal discharge for one year duration, He also reported nasal pain and headache. He gave history of nasal surgery inform of endoscopic partial inferior turbunectomy 3 months prior to his present complain. Anterior rhinoscopy revealed bilateral septal swelling prominently left side, lead to septum deviation to the right side. Endoscopic examination couldn’t be done because there was no space to pass the scope from either side of the nasal cavity. The rest of the otolaryngologic examination including cranial nerve examination and ophthalmic examination was normal.
Radiological investigation was done, Computed tomography (CT) with contrast (Figure.1) and magnetic resonance imaging (MRI) to role out intracranial involvement (Figure 2 and 3) showed a large midline septal mass without intracranial extension.
The patient underwent endoscopic drainage and total excision of the mass under general anaesthesia. The mucocele was filled with mucoid fluid and was drained out, there were no remnants of cartilage or bony septum identified within the septal mucocele, it was excised completely and sent for histopathological evaluation. Nasal pack was applied and taken out after one day. The lesion was confirmed by histopathology as a benign cyst consistent with mucous cyst. During the 6-month-follow-up there was no recurrence confirmed by serial endoscopies and the patient has no complain.
DISCUSSION
Langenback first described mucoceles in 1819, but it was Rollet who introduced the term mucocele in 1896 and Turner differentiated the frontal from the ethmoidal lesion.1
Paranasal mucoceles are benign lesions with the potential for adjacent bony remodeling and resorption. They have a slow growing pattern but they can destroy neighboring structures by compression and expansion. They can take many years for them to become symptomatic.2
Mucoceles primarily occur in the frontal sinuses (60-65%), but may also be found in ethmoid sinuses (20-25%), maxillary sinuses (10%) and sphenoid sinuses (1-2%).6 Paranasal sinuses mucoceles may be found in atypical locations, such as nasal eptum ,nasolacrimal duct, intersinus cell, orbital floor, root of the nose, pterygomaxillary space and middle turbinate in a concha bullosa.2-8
The exact etiology and pathogenesis of mucoceles still remain uncertain. Usually mucoceles are post-inflammatory complications (allergy, chronic infection, chronic inflammatory condition, mucociliary dysfunction) but less usually, may be secondary to neoplastic obstruction (osteoma, juvenile nasoangiofibroma, carcinoma), inflammatory processes (caldwell- Luc procedure) and post-traumatic processes (iatrogenic accidents), generally with long-term progression. Traumas and pneumatoceles were seen as most common etiologic factors for mucocele of the nasal septum. Trauma can be surgical, such as nasal surgery with or without septoplasty like our patient we are presenting, and non-surgical such as foreign body.4,6,7
Nasal septal mucocele are usually diagnosed before destroying the surrounding tissues, due to the relatively early symptomatic because of anatomic localization. High resolution computedtomography scan (HRCT) is the preferred diagnostic imaging modality. On HRCT, mucoceles appear as a homogenous round or oval mass with surrounding bony erosion. The differentiation between a mucocele versus an expansile mass may be made with magnetic resonance imaging (MRI). MRI is helpful in clarifying soft tissue extension to the cranium and orbit. It also helps in differentiating from other soft tissue masses with potentially similar presentation such as meningocele, rhab-domyosarcoma, hemangioma, and neuroblastoma.4-9
The cyst is mainly lined by pseudostratified ciliated columnar or cuboidal epithelium but sometimes it may be lined with areas of squamous epithelium. There is cellular infiltrate comprising neutrophils, lymphocytes, plasma cells, and eosinophils. Subepithelial lymphoid aggregates and vascularity are also seen. Osseous elements are woven bone, lamellar bone, osteoblasts, and osteoclasts.8 Our histopathology report showed a nasal tissue with cystic space lined by flattened epithelium with focal areas showing hyperplasia of respiratory epithelium with chronic inflammatory cells.
All six reported cases have been successfully treated via surgery with endoscopical approach. Gall et al, Hermann et al and Lei et al performed partial excision and marsupialization in their cases. Yılmaz et al and Taşkın et al reported that they excised the mucocele completely. There was no reported complication or recurrence after treatment in literature for nasal mucoceles.4-7 In our case we excised the septal mucocele endoscopically this technique allows the operation to be performed under direct visualization with minimum mucosal trauma and bleeding.
CONCLUSION
Mucocele of the nasal septum is rare but should be considered as one of the differential diagnosis of midline intra nasal masses. Previous nasal surgery with or without septoplasty (foreign body removed, sinus surgery and rhinoplasy) has been reported as case of septal mucocele. Our case demonstrates unique location for a mucocele following inferior turbunectomy.
Funding: No funding sources
Conflict of interest: None declared
Ethical approval: Not required
REFERENCES
- 1. Evans C. Aetiology and treatment of fronto-ethmoidal mucocele. J Laryngol Otol. 1981, 95:361-75.
- 2. Lund VJ, Milroy CM. Fronto-ethmoidal mucocoeles: a histopathological analysis. J Laryngol Otol. 1991;105(11):921-3.
- 3. Har-El G. Endoscopic management of 108 sinus mucoceles. Laryngoscope. 2001;111:2131-4.
- 4. Gall R, Witterick I. Mucocele of the nasal septum. J Otolaryngol. 2002;31(4):246-7.
- 5. Marambaia O, Gomes AM, Marambaia PP, Pinheiro M, Almeida FSC. Tratamento endoscópico das mucoceles frontoetmoidais. Rev Bras Otorrinoloaringol. 2008;74(Supl 1).
- 6. Tinoco P, Pereira JC, Filho LRC, Silva FBD. Tratamento nasoendoscópico da mucocele de seio esfenoidal. Arq Int Otorrinolaringol. 2009;13(3):336-9.
- 7. Taskin U, Korkut YA, Aydin S, Oktay FM. Atypical presentation of primary giant nasal septal mucopyocele. J Craniofac Sur. 2012;23(1):e5-7.
- 8. de Carvalho BV, Lopes IDC, Corrêa JD, Ramos LFM, Motta EGPC, Diniz RLFC. Typical and atypical presentations of paranasal sinus mucocele at computed tomography Radiol Bras. 2013;46(6):372-5.
- 9. Aslan G, Ugur MB, Başsüllü N. Giant mucocele originating from the middle concha in a 5-year-old child: a case report. Journal of Medical Case Reports. 2013;7:246.