Upload
karina-mega-w
View
214
Download
0
Embed Size (px)
Citation preview
7/24/2019 Journal THT ArchIntSurg53184-4250901_114829
1/3
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]
[Downloaded free from http://www.archintsurg.org on Thursday, February 18, 2016, IP: 120.191.167.231]
7/24/2019 Journal THT ArchIntSurg53184-4250901_114829
2/3
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
7/24/2019 Journal THT ArchIntSurg53184-4250901_114829
3/3
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.
References
1. Thorup C, Sebbesen L, Dan H, Leetmaa M, Andersen M,Buchwald C, et al.Carcinoma of the nasal cavity andparanasal sinuses in Denmark 1995-2004. Acta Oncol2010;49:389-94.
2. Wildbrett P, Horras N, Lode H, Warzok R, Heidecke CD,
Barthlen W. Mucoepidermoid carcinoma of the lung in a
6-year-old boy. Afr J Paediatr Surg 2012;9:159-62.
3. Weinstein IR, Nagai I, Yamanaka H. Mucoepidermoid tumor
of the maxilla. Report of a case. Oral Surg Oral Med Oral
Pathol 1967;23:1-11.
4. Barce llos AN, Carvatho CP, Teixeira DC, Machad AP,
Barreiros AC, Barcellos TN. A rare case of MEC of the nasal
septum. Int Arch Otorhinolaryngol 2008;25:582-6.5. Gnepp DR, Heffner DK. Mucosal origin of sinonasal tract
adenomatous neoplasms. Mod Pathol 1989;2:365-71.
6. Thomas GR, Regalado JJ, McClinton M. A rare case of
mucoepidermoid carcinoma of the nasal cavity. Ear Nose
Throat J 2002;81:519-22.
7. Wolfish EB, Nelson BL Thompson LD. Sinonasal tract MEC: A
clinico-pathologic and immunophenotypic study of 19 cases
combined with a comprehensive review of the literature.
Head Neck Pathol 2011;12:1-17.
8. Kazelson DJ, Schindel J. MEC of the air passages: Report of
three cases. Laryngoscope 1979;89:115-21.
9. Ezsis A, Sugar AW, Milling MA, Ashley KF. Centra l
mucoepidermoid carcinoma in a child. J Oral Maxillofac
Surg 1994;52:512-5.
10. Simpson RJ, Hoang KG, Hyams VJ, Jarcho w RC.
Mucoepidermoid carcinoma of the maxillary sinus.
Otolaryngol Head Neck Surg 1988;99:419-23.
[Downloaded free from http://www.archintsurg.org on Thursday, February 18, 2016, IP: 120.191.167.231]