DSpace Repository

Isolated polypoid ganglioneuroma of gall bladder-a case report

Show simple item record

dc.contributor.author Grampurohit, Vandana U.
dc.contributor.author Rao, Ravikala V.
dc.contributor.author Dinesh, U. S.
dc.date.accessioned 2012-08-25T09:00:47Z
dc.date.available 2012-08-25T09:00:47Z
dc.date.issued 2011
dc.identifier.citation Al Ameen Journal of Medical Science. 2011; 4(3): 295-298. en_US
dc.identifier.issn 0974-1143
dc.identifier.uri http://hdl.handle.net/123456789/33
dc.description.abstract A ganglioneuroma is a very rare neoplasm in the gastrointestinal tract and a benign neoplasm of sympathetic nervous system. They predominantly affect the colon and rectum and are rare to arise in gall bladder. Gastrointestinal ganglioneuromas occur as rare isolated (solitary) polypoid lesions or more commonly as ganglioneuromatous polyposis and diffuse ganglioneuromatosis. Isolated polypoid lesions are clinically asymptomatic and incidentally detected during endoscopy or surgery. We report a case of a 42-year-female who presented clinically with features of chronic cholecystitis and was operated. There was no association of any hereditary disease. Incidentally the cholecystectomy specimen showed a small sessile polypoid lesion. Histopathological examination showed the lesion to be polypoid ganglioneuroma arising in gall bladder. The isolated polypoid ganglioneuroma is invariably benign. They do not have increased risk of von Recklinghausen’s disease or multiple endocrine neoplasia IIB and show no evidence of recurrence with excellent prognosis after total excision. en_US
dc.language.iso en en_US
dc.publisher Al Ameen Medical College, Bijapur en_US
dc.subject Gall bladder en_US
dc.subject Isolated en_US
dc.subject Polypoid en_US
dc.subject Ganglioneuroma en_US
dc.title Isolated polypoid ganglioneuroma of gall bladder-a case report en_US
dc.type Article en_US


Files in this item

This item appears in the following Collection(s)

Show simple item record

Search DSpace


Advanced Search

Browse

My Account