Ampullary Neuroendocrine Tumor With Multiple Gastrointestinal Stromal Tumors in a Patient with Von Recklinghausen’s Disease Patient: A Case Report

Von Recklinghausen’s disease (VRD) is a hereditary disease that occurs because of mutation in NF1 gene located on chromosome 17. About 25% of VRD patients are reported to suffer from gastrointestinal lesions varying from hyperplasia of the gut neural tissue, endocrine tumors of the duodenum and the...

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Bibliographic Details
Main Authors: Rakesh Kumar Gupta, Utpal Anand, Kunal Parasar, Mamta Kumari, Punam Prasad Bhadani
Format: Article
Language:English
Published: Wolters Kluwer Medknow Publications 2019-01-01
Series:MAMC Journal of Medical Sciences
Subjects:
Online Access:http://www.mamcjms.in/article.asp?issn=2394-7438;year=2019;volume=5;issue=1;spage=24;epage=28;aulast=Gupta