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Mucopolysaccharidosis I and intracranial tumor in a patient with high-pressure hydrocephalus.

作者信息

Stöckler S, Kleinert R, Ebner F, Paschke E

机构信息

Department of Pediatrics, University of Graz, Austria.

出版信息

Pediatr Radiol. 1993;23(5):353-4. doi: 10.1007/BF02011955.

Abstract

In a 19-month-old patient with mucopolysaccharidosis I (Pfaundler-Hurler, MPS I/H) high-pressure hydrocephalus required the implantation of a ventriculo-peritoneal shunt. Despite a reduction in both ventricular volume and intracranial pressure, clinical symptoms suggesting compression of the brain stem persisted. Brain MRI revealed a tumor within the posterior cranial fossa. Cytologic examination of the cerebrospinal fluid was suggestive of a poorly differentiated ependymoma. High-pressure hydrocephalus is a common complication in MPS I/H. As changes in mucopolysaccharide metabolism may be associated with an increased risk of developing neoplasms, the possibility of an intracranial tumor should be considered in patients with MPS I/H and high-pressure hydrocephalus.

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