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

• 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: Ampullary neuroendocrine tumor; gastrointestinal stromal tumor; NF1 gene; Von Recklinghausen’s disease
• Online Access: http://www.mamcjms.in/article.asp?issn=2394-7438;year=2019;volume=5;issue=1;spage=24;epage=28;aulast=Gupta

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 periampullary region, and gastrointestinal stromal tumors. Herein, we describe a case of ampullary neuroendocrine tumor with unique histology and immunohistochemistry in a 35-year-old male patient with VRD, detailed review of literature.