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±èÃæÇö/Choong Hyun Kim ¹é±¤Èì/±èÀç¹Î/±è¿µ¼ö/°í¿ë/¿À¼®Àü/±è±¤¸í/±è³²±Ô/Kwan Heum Paik/Jae Min Kim/Young Soo Kim/Yong Koh/Suck Chon Oh/Kwang Myung Kim/Nam Kyu Kim

Abstract

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In order to analyze clinical presentations and surgical outcome, we studied eleven
cases of cerebellar hemangioblastoma from among a series of 421 intracranial tumors
treated over a period of seven years.
The proportion of male patients was 2.7 time that of females and the age peak
appeared between 30 and 50 years(mean age : 37.7 years old). The common clinical
presentations were headache(73%), dizziness(55%), unilateral cerebellar dysfunction(45%),
and nausea or vomiting(36%). In our serious there were two cases of cranial nerve
palsy associated with von Hippel-Lindau(VHL) disease. Polycythemia that normalized
postoperatively appeared in two of eleven cases. Radiologic studies showed nine cystic
tumors, six in the cerebellar hemisphere and three in the cerebellar vermis, and three
solid tumors extended into the brain stem.
After aspiration of the cyst, careful removal of the mural nodule gave good results in
more than 70% of patients. Because the tumor extended into the brain stem, however,
three solid lesions were resected subtotally. Postoperative complications developed in four
patients, and in three of these, the lesion extended into the brain stem.
In conclusion, major clinical features were due to increased intracranial pressure, and
varying expression of cerebellar and cranial nerve deficits was characteristic. To
determine the resectability of lesions and to minimize surgical morbidity, extremely
careful clinical and neuroradiological observation is essential.

Å°¿öµå

Hemangioblastomas; Cerebellum; Headache; Polycythemia;

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