TY - JOUR
T1 - Smooth muscle tumour of uncertain malignant potential (SMTUMP) in the nasal cavity
T2 - An incidental finding
AU - Nayak, Dipak Ranjan
AU - Ghanpur, Asheesh Dora
AU - Reddy, Apoorva N.
AU - Sharma, Swati
PY - 2016/1/1
Y1 - 2016/1/1
N2 - Sino-nasal smooth muscle tumours of uncertain malignant potential (SMTUMP) are very rare neoplasms of mesenchymal origin with features in between a benign leiomyoma and a leiomyosarcoma. We report a rare case of SMTUMP in a 44-year-old woman, who presented with vague symptoms of pharyngitis. Nasal endoscopy revealed a smooth mass in left nasal cavity. Contrast-enhanced CT and MRI scans showed features likely to be inverted papilloma or olfactory neuroblastoma or meningioma. Excision was planned and intraoperatively, frozen section revealed a probable spindle cell lesion. Final histopathological report following immunohistochemistry (IHC) & immunofluoresence (IF) confirmed it to be a SMTUMP. This patient underwent complete resection via endoscopic KTP laser assisted, anterior skull base surgery with no recurrence on follow-up.
AB - Sino-nasal smooth muscle tumours of uncertain malignant potential (SMTUMP) are very rare neoplasms of mesenchymal origin with features in between a benign leiomyoma and a leiomyosarcoma. We report a rare case of SMTUMP in a 44-year-old woman, who presented with vague symptoms of pharyngitis. Nasal endoscopy revealed a smooth mass in left nasal cavity. Contrast-enhanced CT and MRI scans showed features likely to be inverted papilloma or olfactory neuroblastoma or meningioma. Excision was planned and intraoperatively, frozen section revealed a probable spindle cell lesion. Final histopathological report following immunohistochemistry (IHC) & immunofluoresence (IF) confirmed it to be a SMTUMP. This patient underwent complete resection via endoscopic KTP laser assisted, anterior skull base surgery with no recurrence on follow-up.
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U2 - 10.1136/bcr-2016-217386
DO - 10.1136/bcr-2016-217386
M3 - Article
C2 - 27879303
AN - SCOPUS:85002131841
SN - 1757-790X
VL - 2016
JO - BMJ Case Reports
JF - BMJ Case Reports
M1 - 217386
ER -