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 3. Functional and nuclear imaging. (A) I123 MIBG SPECT/CT axial image of the abdomen showing an MIBG avid nodule correlating to the left adrenal mass. (B) 68Ga-DOTATOC PET/CT coronal section showing DOTATOC avidity in the pancreatic head and a left thyroid nodule (yellow arrows).

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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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