From WikiCNS
Jump to: navigation, search
Checkmark.gif This article has been reviewed by the NeuroWiki Editorial Board

  1. 10% of patients with vonHippel Lindau (VHL) have pheochromocytoma while 23% of patients diagnosed initially as having pheochromocytoma will have either the VHL complex or multiple endocrine neoplasia (MEN) IIa
  2. 10% of pheochromocytomas are malignant
  3. symptoms due to catecholamine (epinephrine and norepinepherine) secretion and include: episodic headaches, excessive sweating, palpitation, nervousness, and tremor; headaches in a patient with VHL may be due to cerebellar tumor with increased intracranial pressure or to catecholamine excess from the pheochromocytoma; blood pressure may rise greatly during procedure for pheochromocytoma
  4. best screening test: urinary metanephrine assay; may also screen with vanillylmandelic acid (VMA) and catecholamines
  5. treatment: resection with a 90% cure rate
Personal tools