• Carlos Alfredo Mena-Cedillos, Adriana M Valencia-Herrera, Alma Iris Arroyo-Pineda, M Angeles Salgado-Jiménez, Rubén Espinoza-Montero, Armando Bernardo Martínez-Avalos, and Antonio Perales-Arroyo.
• Department of Dermatology, Federico Gómez Children's Hospital of Mexico, Mexico City, Mexico.
• Pediatr Dermatol. 2002 May 1;19(3):237-42.

AbstractNeurocutaneous melanosis is a rare congenital neurocutaneous syndrome in which benign and malignant melanocytic tumors of the leptomeninges with large or numerous congenital melanocytic nevi develop. The Dandy-Walker malformation occurs as a broad posterior fossa with high insertion of the tentorium, hypoplasia or aplasia of the cerebellar vermis, and cystic dilation of the fourth ventricle communicating with the posterior fossa. Association of these entities is very unusual and only 10 previous reports were found in the literature. Our patient had multiple, medium-size to small melanocytic nevi present since birth. At 5 years of age the patient has intracranial pressure secondary to hydrocephalus. A diagnosis of Dandy-Walker malformation and suspected neurocutaneous melanosis was established after a skull computed tomography (CT) scan. Three months later the patient developed a right frontal tumor shown on the CT scan. The histologic finding was nevomelanocytic infiltration with strong pleomorphism. The tumor grew rapidly, producing neurogenic shock and death. The postmortem report indicated malignant melanoma.

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