ADENOID CYSTIC CARCINOMA IN SINONASAL CAVITY – AN UNUSUAL SITE OF CASE PRESENTATION
Dr. Krishna Priya R., Sunderesh Kamal Chander U.*, Dr. Rajeswar K. and Dr. Sonti Sulochana
Abstract
Adenoid cystic carcinoma is a relatively rare tumor of epithelial cell
origin, most commonly arising from major or minor salivary glands,
and comprises 3 to 5% of all head and neck malignant tumors. The
peak incidence is from the fourth decade to the sixth decade, occurring
slightly more in females. It usually presents as a slowly growing, firm
mass, and patients most commonly report a constant, low-grade dull
ache that gradually worsens in severity. Here we reported a 55 years
old female presented with complaints of left nasal block, left sided
headache aggravated on cold food for 6 months. Local examination of
the nasal cavity revealed normal external framework and septum
showed mild DNS to the left with spur. Anterior rhinoscopy- DNS to
left with spur. Posterior rhinoscopy showed left nasal mass. CT
paranasal sinuses showed a polypoidal lesion mildly enhancing
irregular soft tissue density involving the left nasal cavity with erosion/resorption of adjacent
bones – likely to be malignant neoplastic etiology. On histopathological examination features
suggested Adenoid cystic carcinoma. Hence we presented this case report due to it’s site
rarity.
Keywords: Adenoid cystic carcinoma, Sinonasal malignancies, epithelial cell tumors, cribriform pattern tumor and hadron therapy.
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