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Neuroendocrine Tumors

Joseph Mort
  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.
AccessMedicine > Harrison's Principles of Internal Medicine, 20e > Neuroendocrine Tumors of the Gastrointestinal Tract and Pancreas
AccessMedicine > Harrison's Principles of Internal Medicine, 20e > Pheochromocytoma
AccessMedicine > Harrison's Principles of Internal Medicine, 20e > Multiple Endocrine Neoplasia
Case File
AccessMedicine > Pathophysiology of Disease Cases > Case 18 > Carcinoid Syndrome from Neuroendocrine Tumer (NET)


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