Neurofibroma of Maxillary Sinus: A Rare Case Report

2010 ◽  
Vol 3 (2) ◽  
pp. 123-125
Author(s):  
Arjun Dass ◽  
Surinder Singhal ◽  
Meenakshi G Bansal

Abstract Neurofibroma is a tumor of neuronal origin. Solitary neurofibroma of maxillary sinus is exceedingly rare tumor.

2016 ◽  
Vol 5 (3) ◽  
pp. 265
Author(s):  
Vagish KumarLaxman Shanbhag ◽  
Riaz Abdulla ◽  
Surendranathan Akhila ◽  
Maji Jose

2017 ◽  
Vol 29 (4) ◽  
pp. 341 ◽  
Author(s):  
Anuj Mishra ◽  
Abhishek Sinha ◽  
Anusha ◽  
PoojaM Sinha

2017 ◽  
Vol 5 (3) ◽  
pp. 129-134
Author(s):  
Dr.N.V.V.Satya Bhushan ◽  
◽  
Dr.U.Siva Kalyan ◽  
Dr.KhoChai Chiang ◽  
Dr.K.Bramara Kumari ◽  
...  

2013 ◽  
Vol 5 (2) ◽  
pp. 19-20
Author(s):  
SG Smitha ◽  
Smitha Soubhagya Gangaraj ◽  
Lakshmi Shantharam ◽  
Suguna Vijay

ABSTRACT Neurofibroma of soft palate is a rare tumor with this report being the fourth case reported in English literature. We are reporting this case of isolated neurofibroma of soft palate for its rarity. The mass was excised by intraoral approach without prior tracheostomy. Histopathological examination showed features of neurofibroma with secondary changes.


2020 ◽  
Vol 11 (S1) ◽  
pp. 73-77
Author(s):  
Abhinav Deshpande ◽  
Ankita Tamhane ◽  
Y. S. Deshpande ◽  
Radhika Pagey ◽  
Meena Pangarkar

Abstract Introduction Mesenteric fibromatosis-desmoid tumor of mesentery is a rare benign soft tissue tumor of mesentery. On CT, it mimics gastrointestinal stromal tumor (GIST). Case Report A 44-year-old female with small intestinal mass, preoperatively diagnosed radiologically and pathologically as GIST. Conclusion Mesenteric fibromatosis is a rare tumor often mistaken for GIST. Histopathology and immunohistochemistry is the key as management of both the tumors differs.


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