Phaeochromocytoma

Author: Rob Stafford / Editor:Tajek B Hassan / Reviewer: Emma Everitt, Rob Stafford / Codes: A1, O7 / Published: 13/09/2021

Description:

Describing the key features relevant to the history of phaeochromocytoma

After completing this session you will be able to:

  • Describe the key features relevant to the history of phaeochromocytoma
  • Describe the pathophysiological mechanism by which phaeochromocytoma causes its clinical features
  • Understand that phaeochromocytoma can mimic common emergency department presentations
  • Outline the generic aspects of the management of phaeochromocytoma

References:

  1. Platts JK, Drew PJ, Harvey JN. Death from phaeochromocytoma: lessons from a post-mortem survey. J R Coll Physicians Lond. 1995 Jul-Aug;29(4):299-306.
  2. Anderson GH Jr, Blakeman N, Streeten DH. The effect of age on prevalence of secondary forms of hypertension in 4429 consecutively referred patients. J Hypertens. 1994 May;12(5):609-615.
  3. Whalen RK, Althausen AF, Daniels GH. Extra-adrenal pheochromocytoma. J Urol. 1992 Jan;147(1):1-10.
  4.  Pacak K, Linehan WM, Eisenhofer G et al. Recent advances in genetics, diagnosis, localization, and treatment of pheochromocytoma. Ann Intern Med. 2001 Feb 20;134(4):315-329.
  5. Neumann HP, Berger DP, Sigmund G et al. Pheochromocytomas, multiple endocrine neoplasia type 2, and von Hippel-Lindau disease. N Engl J Med. 1993 Nov 18;329(21):1531-8. Erratum in: N Engl J Med 1994 Dec 1;331(22):1535.
  6. Ramrakha P, Moore K.  Oxford Handbook of Acute Medicine, Oxford,  2004.

Resources:

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