J Korean Neurosurg Soc.  1997 Apr;26(4):571-577.

Von Hippel-Lindau Disease Manifestating as Recurrent Cerebellar Hemangioblastoma: A Case Report

• Yoo KU
• Jung CK
• Lee IW
• Choi CM
• Yang JH
• Park CK
• Lee SW
• Kang JK

Abstract

Cerebellar hemangioblastoma comprises 2% of all brain tumors and 7% 10% of all posterior fossa tumors. It can arise in isolation("sporadic cases") or as a major manifestation of von Hippel-Lindau(VHL) disease, a well known autosomal dominant inherited tumor syndrome. Only 5-30% of these tumors are due to VHL disease. However, cerebellar hemangioblastoma occurs in younger patients, is often multiple and recurrent, and has a poorer prognosis than sporadic cases. We present a case of a 26-year-old woman with a right cerebellar hemangioblastoma, which recurred from a left cerebellar hemangioblastoma resected four years previously. Further evaluation established the diagnosis of VHL disease by demonstrating a cystadenoma in the pancreas and an omental cyst. Recently, the von Hippel-Lindau disease gene has been identified as a tumor suppressor gene and has been mapped to the short arm of chromosome 3(3p 25-26). Its absence or a defect in its structure is responsible for predisposition to the disease.

Keyword

Recurrent Hemangioblastoma; von Hippel-Lindau disease; Tumor suppressor gene; Cystadenoma; Omental cyst

MeSH Terms

Adult
Arm
Brain Neoplasms
Cystadenoma
Diagnosis
Female
Genes, Tumor Suppressor
Hemangioblastoma*
Humans
Infratentorial Neoplasms
Pancreas
Prognosis
von Hippel-Lindau Disease*