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Neuroendocrine Tumors

AUTHOR:
Joseph Mort
LEARNING OBJECTIVES:
  1. Know the pathologic conditions and inheritance pattern associated with MEN1, MEN2A, and MEN2B.
  2. Recognize the clinical presentation of pheochromocytoma.
  3. Know the treatment of pheochromocytoma and the correct order of medication administration to prevent cardiovascular complications.
  4. List the different types of GI/pancreatic neuroendocrine tumors and explain their clinical presentation through consideration of their secretory products.
  5. List the features of carcinoid syndrome and explain the anatomic requirement that must be met for a patient to develop this condition.
Section
AccessMedicine > Huppert’s Notes: Pathophysiology and Clinical Pearls for Internal Medicine > OTHER CONDITIONS THAT AFFECT THE SMALL BOWEL > Carcinoid syndrome
Section
AccessMedicine > Huppert’s Notes: Pathophysiology and Clinical Pearls for Internal Medicine > GASTROINTESTINAL MALIGNANCIES > Pancreatic neuroendocrine tumors (PNET)
Section
AccessMedicine > Huppert’s Notes: Pathophysiology and Clinical Pearls for Internal Medicine > ADRENAL GLAND > Pheochromocytoma
Chapter
AccessMedicine > The MD Anderson Manual of Medical Oncology, 4e > Neuroendocrine Tumors
Chapter
AccessMedicine > Current Medical Diagnosis & Treatment 2024 > Pheochromocytoma & Paraganglioma
Case File
AccessMedicine > Pathophysiology of Disease Cases > Case 18 > Carcinoid Syndrome from Neuroendocrine Tumer (NET)
Case File
AccessMedicine > Pathophysiology of Disease Cases > Case 66 > Pheochromocytoma
Section
AccessMedicine > The Infographic Guide to Medicine > Endocrinology > Multiple Endocrine Neoplasia
Section
AccessMedicine > The Infographic Guide to Medicine > Endocrinology > Adrenal Neoplasm

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