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Involvement of the skull base and vault in chronic idiopathic hyperphosphatasia
Authors:Laura Mazzanti  Paolo Ambrosetto  Rolando Libri  Raffaele Pascarella  Antonio Balsamo  Gianni Tani
Affiliation:(1) 1st Paediatric Clinic, University of Bologna, Bologna, Italy, IT;(2) Neurology Clinic, University of Bologna, Bologna, Italy, IT;(3) Rizzoli Orthopaedic Institute, Bologna, Italy, IT;(4) Paediatric Radiology Service, S. Orsola Hospital, Bologna, Italy, IT;(5) Paediatric Radiology Service, University of Bologna, Via Massarenti 11, I-40 138 Bologna, Italy, IT
Abstract:Chronic idiopathic hyperphosphatasia (CIH) is a rare generalised skeletal dysplasia in childhood. The clinical, radiographic and cerebral MR findings in a 5-year-old girl with the severe infantile form of CIH are reported. In spite of cranial enlargement, the intracranial space and the skull base were markedly reduced, the whole brain was compressed and a Chiari I malformation was present. Normal flow in the dural venous sinuses was documented. The patient showed no detectable cranial nerve involvement or hydrocephalus. Cranial MR in this patient enabled us to confirm that CIH involves the skull base and vault. Received: 19 December 1997 Accepted: 17 April 1998
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