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Lipomatosis encefalocraneocutánea: reporte de caso
Juan Pablo Muñoz-Montufar1, Jesús Darío Rayo-Mares1, Araceli Reyes-Cuayahuitl1
1Servicio de Neurología Pediátrica; Unidad Médica de Alta Especialidad Hospital de Pediatría Dr. Silvestre Freunk Freund, Centro Médico Nacional Siglo XXI, Instituto Mexicano del Seguro Social, México, México.
Abstract:
The encephalocraniocutaneous lipomatosis (ECCL), also known as Fishman or Haberland syndrome, is a rare neurocutaneous syndrome of unknown etiology. Clinically characterized by skin, eye and central nervous system lesions. We present the case of a 7-year-old female who presents to the outpatient clinic of Pediatric Neurology because of the presence of seizures detecting clinical and neuroimaging manifestations compatible with ECCL. The objective of this article is to present the case because of its rare presentation and the variety of alterations found in the tomography.
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