Coexistence of Gastrointestinal Stromal Tumors (GISTs) and Pheochromocytoma in Three Cases of Neurofibromatosis Type 1 (NF1) with a Review of the Literature
Author:
Affiliation:
1. Department of Endocrinology and Metabolism, Ataturk Training and Research Hospital, Turkey
2. Department of Medical Pathology, Ataturk Training and Research Hospital, Turkey
Publisher
Japanese Society of Internal Medicine
Subject
General Medicine,Internal Medicine
Link
https://www.jstage.jst.go.jp/article/internalmedicine/53/16/53_53.2012/_pdf
Reference28 articles.
1. 1. Fletcher CD, Berman JJ, Corless C, et al. Diagnosis of gastrointestinal stromal tumors: A consensus approach. Hum Pathol 33: 459-465, 2002.
2. 2. Costi R, Caruana P, Sarli L, et al. Ampullary adenocarcinoma in neurofibromatosis type 1. Case report and literature review. Mod Pathol 14: 1169-1174, 2001.
3. 3. NIH Consensus Development Conference Statement: Neurofibromatosis conference statement. Arch Neurol 45: 575-578, 1988.
4. 4. Fitzgerald PA. Adrenal Medulla and Paraganglia. In: Greenspan's Basic & Clinical Endocrinology. 9th ed. (s.364). Gardner DG, Shoback D, Eds. The McGraw-Hill, Minneapolis, MN, 2011.
5. 5. Basile U, Cavallaro G, Polistena A, et al. Gastrointestinal and retroperitoneal manifestations of type 1 neurofibromatosis. J Gastrointest Surg 14: 186-194, 2010.
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