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    184 2015 Archives of International Surgery | Published by Wolters Kluwer - Medknow

    Mucoepidermoid carcinoma of the nasal cavitymimicking a simple nasal polyp

    ABSTRACT

    Mucoepidermoid carcinoma (MEC) of the sinonasal area is very rare and frequently misclassified. We report a 43-year-old woman

    who presented with persistent nasal blockage, epistaxis, progressive right cheek swelling and ipsilateral proptosis. The affected

    eyes vision was low, to identifying only fingers at 6 m. She also had hypoesthesia over the right cheek and distortion of the

    ipsilateral external nasal pyramid. There was also a fleshy mass filling the right nasal cavity, causing the deviation of the nasal

    septum to the contra-lateral side. A diagnosis of a malignant nasal mass was made. Following the nasal polypoidal mass biopsy a

    histological diagnosis of MEC was made. The patient had complete evaluation including computed tomography scan of the sinuses

    and underwent extensive surgical resection and postoperative radiotherapy. The patient is doing well on follow-up.

    Key words:Mucoepidermoid carcinoma, nasal polyp, sinonasal carcinoma

    Tokan Silas Baduku, Saadatu Ladan1, Mainasara Mohammed1, Joshua Jibrin1

    Department of Radiology, Kaduna State University, Kaduna, 1National Ear Care Centre, Kaduna, Nigeria

    Address for correspondence:Dr. Tokan Silas Baduku,

    Department of Radiology, Kaduna State University, Kaduna, Nigeria.E-mail: [email protected]

    Access this article online

    Quick Response Code:Website:

    www.archintsurg.org

    DOI:

    10.4103/2278-9596.167519

    Case Report

    Treatment options include surgery, radiation therapy, and

    chemotherapy. A combination of these will produce more

    excellent results.

    We present the case of a 43-year-old female with sinonasal

    MEC that mimicked a simple nasal polyp, but histology

    gave a diagnosis. She was successfully operated upon andsubsequently referred for radiotherapy.

    Case Report

    A 43-year-old female presented with a 4-year history

    of recurrent rhinorrhea, and 3-year history of bilateral

    alternating nasal blockage, worse in the right nasal

    cavity, which had become persistent 6 months prior to

    the presentation. She had associated blood-tinged nasal

    discharge, postnasal drip, hyposmia, and hyponasal

    Introduction

    Mucoepidermoid carcinoma (MEC) is a common malignant

    neoplasm of the salivary gland, with the parotid being the

    main site of occurrence.[1]However, the sinonasal location

    of this tumor is extremely rare,[2]constituting only 0.6%

    of all MECs.[3]

    Mucoepidermoid carcinoma is defined bythe WHO as a malignancy consisting of mucous-secreting

    squamous and intermediate cell types, usually arising

    from the squamous, mucus-secreting cells of the salivary

    glands, but can also be found in other organs such as the

    lacrimal sac, larynx, lungs, thyroid, and the sinonasal

    tract.[1]The management of MEC depends on its grade,

    location and the extent of spread. Early diagnosis gives a

    better prognosis. Also, a low-grade tumor will generally

    have a good prognosis compared with a high-grade tumor.

    How to cite this article:Baduku TS, Ladan S, Mohammed M, Jibrin J.

    Mucoepidermoid carcinoma of the nasal cavity mimicking a simple nasal

    polyp. Arch Int Surg 2015;5:184-6.

    This is an open access article distributed under the terms of theCreative Commons Attribution-NonCommercial-ShareAlike 3.0

    License, which allows others to remix, tweak, and build upon the

    work non-commercially, as long as the author is credited and the

    new creations are licensed under the identical terms.

    For reprints contact:[email protected]

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    Baduku, et al.: Mucoepidermoid carcinoma of the nasal cavity

    Archives of International Surgery / July-September 2015 / Vol 5 / Issue 3 185

    speech. She is a known hypertensive on antihypertensive

    medication and neither smokes cigarette nor ingests

    alcohol. Initial assessment revealed insensitive polypoidal

    masses filling both nasal cavities that were not friable and

    had no contact bleeding.

    She was sent to the Radiology Department for sinus

    radiographs and computed tomography (CT) sinuses

    during which she absconded for 2 years after which

    she reappeared. She represented with persistent nasal

    blockage, epistaxis, progressive right cheek swelling and

    ipsilateral proptosis. The affected eyes vision was low, to

    identifying only fingers at 6 m. She also had hypoesthesia

    over the right cheek and distortion of the ipsilateral

    external nasal pyramid. There was also a fleshy mass

    filling the right nasal cavity, causing the deviation of the

    nasal septum to the left. There was also tenderness over

    the right maxillary dentition, but no loose teeth, or palatal

    bulge were demonstrated. No cervical lymphadenopathywas seen.

    Plain radiographs showed opacification of all the paranasal

    sinuses and the nasal cavities, more extensive to the right.

    CT showed isodense, poor contrast enhancing masses

    infiltrating the sinuses and the nasal cavities. There was

    an erosion of the frontal, maxillary and nasal bones on the

    right side, with mid-line deviation to the contra-lateral side

    [Figure 1]. The retro-antral fat, pterygoids and the base of

    skull were intact.

    The patient had a wide exenteration of the tumor via anendoscopic approach and was referred for radiotherapy.

    Histology showed an infiltrating tumor growing in singles,

    sheets, tubules and trabeculae. It was composed of

    epithelial cells with dark round nuclei, variable amounts of

    amphophilic to clear cytoplasm. The stroma was lionized

    and collagenous. The conclusion was a mucoepidermoid

    carcinoma (MEC).

    She was referred to the oncology unit where she had

    radiochemotherapy. Follow-up visits to our clinic for the

    last 8 months showed a stable middle-aged woman. She

    is still being followed-up.

    Discussion

    Sinonasal malignancies account for

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    Baduku, et al.: Mucoepidermoid carcinoma of the nasal cavity

    186 Archives of International Surgery / July-September 2015 / Vol 5 / Issue 3

    presented with these symptoms probably because of

    delayed presentation.

    Conclusion

    Sinonasal MEC is a rare tumor entity. Though rare, it should

    be considered among the differentials of nasopharyngeal

    tumors. Histology is required to confirm the diagnosis

    while the tumor responds well to surgical resection and

    radiochemotherapy.

    Financial support and sponsorship

    Nil.

    Conicts of interest

    There are no conflicts of interest.

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