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Hypertension Secondary to Pheochromocytoma

  • William M. Manger
  • Ray W. GiffordJr.
Part of the Developments in Cardiovascular Medicine book series (DICM, volume 16)

Abstract

The clinical expressions of pheochromocytoma are often dramatic and explosive, and are so variable that it has rightly earned the title of the ‘great mimic’ [1]. One cannot determine histologically whether a pheochromocytoma is benign or malignant. Although only 10% of these neoplasms are pathologically malignant, as evidenced by metastasis or invasion of adjacent tissue, lethal complications from the effects of excessive circulating catecholamines (epinephrine and norepinephrine) almost invariably result if the disease is not appropriately treated. All patients with manifestations even remotely suggestive of pheochromocytoma must be screened for this disease.

Keywords

Medullary Thyroid Carcinoma Multiple Endocrine Neoplasia Type Multiple Endocrine Neoplasia Urinary Catecholamine Sustained Hypertension 
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.

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Copyright information

© Martinus Nijhoff Publishers, The Hague 1982

Authors and Affiliations

  • William M. Manger
  • Ray W. GiffordJr.

There are no affiliations available

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