Acquired encephaloceles and epilepsy in osteopetrosis.

Autor: Mandl ES; Department of Neurosurgery, VU University Medical Center, Amsterdam, The Netherlands. es.mandl@vumc.nl, Buis DR, Heimans JJ, Peerdeman SM
Jazyk: angličtina
Zdroj: Acta neurochirurgica [Acta Neurochir (Wien)] 2007 Jan; Vol. 149 (1), pp. 79-81; discussion 81. Date of Electronic Publication: 2006 Dec 28.
DOI: 10.1007/s00701-006-1070-4
Abstrakt: Osteopetrosis is a condition in which there is a defect in bone resorption by osteoclasts. With thickening of the skull and skull base, the cranial capacity becomes compromised and skull foramina gradually occlude, resulting in a wide range of neurological symptoms and signs. We present a case of autosomal dominant osteopetrosis with temporal lobe epilepsy and nasal obstruction due to acquired bifrontal encephaloceles associated with a decreased intracranial capacity. Neurosurgical reconstruction of the frontal skull base alleviated the symptoms of epilepsy and nasal obstruction.
Databáze: MEDLINE