Display Settings:

Format

Send to:

Choose Destination
See comment in PubMed Commons below
BMJ Case Rep. 2013 Jan 22;2013. pii: bcr2012007989. doi: 10.1136/bcr-2012-007989.

Contiguous haemangioblastomas of the brain and spine in a patient of Von Hippel-Lindau disease.

Author information

  • 1Department of Neurosurgery, Bangabandhu Sheikh Mujib Medical University, Dhaka, Bangladesh. bijoun14@yahoo.com

Abstract

Von Hippel-Lindau (VHL) disease is an inherited, autosomal-dominant syndrome caused by heterozygous germline mutations in the VHL gene, and predisposing to the development of benign and malignant tumours and cysts in multiple organ systems involving eyes, kidneys, pancreas, liver and central nervous system. The responsible tumour suppressor gene for VHL disease is in chromosome 3p25. We are presenting a case of a patient with both cerebellar as well as spinal haemangioblastoma in addition to polycystic pancreas. We operated on both the spinal and the cerebellar haemangioblastomas and the patient had made a very good recovery. We present this case for its rarity along with the literature review.

PMID:
23345492
[PubMed - indexed for MEDLINE]
PubMed Commons home

PubMed Commons

0 comments
How to join PubMed Commons

    Supplemental Content

    Full text links

    Icon for HighWire
    Loading ...
    Write to the Help Desk