2020
DOI: 10.1097/mpa.0000000000001618
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The Case of an Asymptomatic Pheochromocytoma Masquerading as a Pancreatic Neuroendocrine Tumor

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Cited by 2 publications
(1 citation statement)
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“…This can be further complicated by the fact that around 10% of pancreatic neuroendocrine tumors are associated with hereditary syndromes like multiple endocrine neoplasia type I (MEN1), von Hippel-Lindau syndrome, neurofibromatosis type 1, and tuberous sclerosis complex (TSC). Preoperative diagnosis can be done through fine-needle aspiration and biopsy, but PGLs and PANNET can have similar morphologic characteristics, leading to misdiagnosis (5)(6)(7)(8). Accurate diagnosis is crucial for proper pre-and post-treatment decision-making (9).…”
Section: Introductionmentioning
confidence: 99%
“…This can be further complicated by the fact that around 10% of pancreatic neuroendocrine tumors are associated with hereditary syndromes like multiple endocrine neoplasia type I (MEN1), von Hippel-Lindau syndrome, neurofibromatosis type 1, and tuberous sclerosis complex (TSC). Preoperative diagnosis can be done through fine-needle aspiration and biopsy, but PGLs and PANNET can have similar morphologic characteristics, leading to misdiagnosis (5)(6)(7)(8). Accurate diagnosis is crucial for proper pre-and post-treatment decision-making (9).…”
Section: Introductionmentioning
confidence: 99%