Pancreatic Gastrinoma, Gastrointestinal Stromal Tumor (GIST), Pheochromocytoma, and Hürthle Cell Neoplasm in a Patient with Neurofibromatosis Type 1: A Case Report and Literature Review

Arif A. Arif; Peter T.W. Kim; Adrienne Melck; Andrew Churg; Zachary Schwartz; Heather C. Stuart

doi:10.12659/AJCR.927761

16 January 2021 : Case report Canada

Pancreatic Gastrinoma, Gastrointestinal Stromal Tumor (GIST), Pheochromocytoma, and Hürthle Cell Neoplasm in a Patient with Neurofibromatosis Type 1: A Case Report and Literature Review

Rare coexistence of disease or pathology

Arif A. Arif^1ADEF, Peter T.W. Kim^2ABDE, Adrienne Melck^2ABDE, Andrew Churg^3ABDE, Zachary Schwartz^4ABDE, Heather C. Stuart^2ABDEFG*

DOI: 10.12659/AJCR.927761

Am J Case Rep 2021; 22:e927761

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Figure 1. Computed tomography scan of the abdomen, showing a 1.7-cm left adrenal mass, a 3.7-cm pancreatic mass with partial calcification, and 1 of numerous cutaneous neurofibromas (annotated in yellow).

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Pancreatic Gastrinoma, Gastrointestinal Stromal Tumor (GIST), Pheochromocytoma, and Hürthle Cell Neoplasm in a Patient with Neurofibromatosis Type 1: A Case Report and Literature Review

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