Isolated Angiitis in the Hypothalamus Mimicking Brain Tumor

    • TSUTSUMI Satoshi
    • Departments of Neurological Surgery, Juntendo University Urayasu Hospital
    • ITO Masanori
    • Departments of Neurological Surgery, Juntendo University Urayasu Hospital
    • KANEDA Kazuhiko
    • Departments of Internal Medicine, Juntendo University Urayasu Hospital

Abstract

A 64-year-old female presented with exaggerating somnolence without contributory medical and lifestyle histories. She was not aware of any preceding infection or headache. Cerebral magnetic resonance imaging demonstrated an isolated enhanced mass in the hypothalamus without meningeal enhancement. Blood and cerebrospinal fluid examinations showed no significant findings except for hypernatremia and hyperprolactinemia. She underwent an open biopsy via the interhemispheric route. Histological examination revealed marked perivascular lymphocytic aggregation with polyclonal immunostaining both for B and T lymphocytes. No findings suggestive of underlying malignancy were recognized. Extensive work-up aiming at systemic vasculitis and lymphoma revealed no signs of extracranial lesion, so the most probable diagnosis was isolated angiitis in the hypothalamus. Angiitis may originate from the hypothalamus and should be considered in the differential diagnosis of hypothalamic lesion mimicking brain tumor on neuroimaging.

Journal

神経外科   [List of Volumes]

神経外科 48(1), 33-36, 2008-01-15  [Table of Contents]

The Japan Neurosurgical Society

References:  21

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Codes

  • NII Article ID (NAID) :
    110006546737
  • NII NACSIS-CAT ID (NCID) :
    AN00358613
  • Text Lang :
    ENG
  • Article Type :
    NOT
  • ISSN :
    04708105
  • Databases :
    CJP  NII-ELS  J-STAGE