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Who is at risk for a pheochromocytoma?

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  • These tumors are more common in people with inherited disorders or conditions, including: Multiple endocrine neoplasia, type II
  • Von Hippel-Lindau disease
  • Neurofibromatosis 1 (NF1)
  • Hereditary paraganglioma syndrome

From: What Is Pheochromocytoma? WebMD Medical Reference

SOURCES:

National Organization for Rare Diseases: “Pheochromocytoma.”

Medscape: “Pheochromocytoma Treatment & Management.”

Johns Hopkins Medicine: “Adrenal Glands.”

UpToDate.com : “Clinical presentation and diagnosis of pheochromocytoma.”

OncoLink (Penn Medicine): “All About Pheochromocytoma.”

Zuber, S. , June 2012. Endocrinology and Metabolism Clinics of North America

Dana Farber Cancer Institute: “Ask the cancer genetics team: inherited tendency for pheochromocytomas.”

University of Maryland Medical Center: “Adrenal Glands.”

Medscape: “Pediatric Pheochromocytoma Treatment & Management.”

Reviewed by Laura J. Martin on July 11, 2018

SOURCES:

National Organization for Rare Diseases: “Pheochromocytoma.”

Medscape: “Pheochromocytoma Treatment & Management.”

Johns Hopkins Medicine: “Adrenal Glands.”

UpToDate.com : “Clinical presentation and diagnosis of pheochromocytoma.”

OncoLink (Penn Medicine): “All About Pheochromocytoma.”

Zuber, S. , June 2012. Endocrinology and Metabolism Clinics of North America

Dana Farber Cancer Institute: “Ask the cancer genetics team: inherited tendency for pheochromocytomas.”

University of Maryland Medical Center: “Adrenal Glands.”

Medscape: “Pediatric Pheochromocytoma Treatment & Management.”

Reviewed by Laura J. Martin on July 11, 2018

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How do doctors diagnose a pheochromocytoma?

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