[Intracranial haemorrhage associated with phaeochromocytoma]

Rev Neurol (Paris). 2004 Oct;160(10):945-8. doi: 10.1016/s0035-3787(04)71078-4.
[Article in French]

Abstract

Introduction: Pheochromocytoma is rarely disclosed by intracranial hemorrhage. We report two cases.

Observation: The first 26-year-old patient developed subarachnoid hemorrhage due to a ruptured aneurysm of the middle cerebral artery. The second patient, aged 44 years, had a temporal hematoma. Diagnosis was suggested in both patients by hypertension and elevated urinary catecholamines and confirmed by imaging and MIBG scintigraphy. Adrenal gland tumors, on both glands in the first patient and on the right gland in the second were successfully removed; cranial hypertension totally regressed. Von Hippel Lindau disease was diagnosed by molecular genetics in the first patient. Paroxysmal hypertension could explain the brain hemorrhage in the first patient and may have favored aneurysmal rupture in the second.

Conclusion: The relationships between pheochromocytoma and cerebral aneurysm are discussed.

Publication types

  • Clinical Trial

MeSH terms

  • Adrenal Gland Neoplasms / complications*
  • Adrenal Gland Neoplasms / diagnostic imaging
  • Adrenal Gland Neoplasms / surgery
  • Adrenalectomy
  • Adult
  • Catecholamines / urine
  • Cerebral Angiography
  • Cerebral Hemorrhage / complications*
  • Cerebral Hemorrhage / surgery
  • Hematoma / etiology
  • Humans
  • Hypertension / complications
  • Intracranial Aneurysm / complications
  • Magnetic Resonance Imaging
  • Male
  • Middle Cerebral Artery / pathology
  • Neurosurgical Procedures
  • Pheochromocytoma / complications*
  • Pheochromocytoma / diagnostic imaging
  • Pheochromocytoma / surgery
  • Radionuclide Imaging
  • Subarachnoid Hemorrhage / etiology
  • Subarachnoid Hemorrhage / pathology
  • Tomography, X-Ray Computed
  • von Hippel-Lindau Disease / diagnosis
  • von Hippel-Lindau Disease / etiology
  • von Hippel-Lindau Disease / genetics

Substances

  • Catecholamines