
![]() |
|||||||||||||
WJPR Citation
|
| All | Since 2020 | |
| Citation | 8502 | 4519 |
| h-index | 30 | 23 |
| i10-index | 227 | 96 |
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. [Full Text Article] [Download Certificate] |
