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J Korean Neurosurg Soc. 2014 Jul;56(1):61-65. English. Case Report. https://doi.org/10.3340/jkns.2014.56.1.61
Sung KS , Song YJ .
Department of Neurosurgery, College of Medicine, Dong-A University, Busan, Korea. ns2000@donga.ac.kr
Abstract

Neurocutaneous melanosis (NCM) is a rare congenital syndrome consisting of benign or malignant melanotic tumors of the central nervous system with large or numerous cutaneous melanocytic nevi. The Dandy-Walker complex (DWC) is characterized by an enlarged posterior fossa with high insertion of the tentorium, hypoplasia or aplasia of the cerebellar vermis, and cystic dilatation of the fourth ventricle. These each two conditions are rare, but NCM associated with DWC is even more rare. Most patients of NCM with DWC present neurological symptoms early in life such as intracranial hemorrhage, hydrocephalus, and malignant transformation of the melanocytes. We report a 14-year-old male patient who was finally diagnosed as NCM in association with DWC with extensive intracerebral and spinal cord involvement.

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