Eur J Pediatr Surg 2008; 18(3): 198-201
DOI: 10.1055/s-2008-1038536
Case Report

© Georg Thieme Verlag KG Stuttgart · New York

Chiari Malformation Caused by Craniometaphyseal Dysplasia: Case Report and Review of Literature

C. Cai1 , 2 , Q. Zhang2 , C. Shen1 , G. Sun3 , C. Wang4
  • 1Department of Neurosurgery, General Hospital of Tianjin Medical University, Tianjin, China
  • 2Department of Neurosurgery, Tianjin Children's Hospital, Tianjin, China
  • 3Department of Endocrinology, Tianjin Children's Hospital, Tianjin, China
  • 4Department of Radiology, Tianjin Children's Hospital, Tianjin, China
Further Information

Publication History

received December 6, 2007

accepted after revision February 12, 2008

Publication Date:
21 May 2008 (online)

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Abstract

Chiari malformation is commonly considered a congenital condition. To our knowledge, reports of progressively symptomatic Chiari Ι malformation with craniometaphyseal dysplasia are rare. The authors present a case of progressively symptomatic Chiari Ι malformation occurring in an 11-month-old infant with craniometaphyseal dysplasia. The patient presented with a typical facial appearance and radiological skeletal survey. Posterior fossa decompression was performed. In the meantime, the patient was given Rocaltrol® (calcitriol) and adopted a low calcium diet. His neurological symptoms were markedly improved after surgery. The clinical presentations, radiographical features and prognosis of the patient are discussed with reference to the literature.

References

Prof. Changhong Shen

Department of Neurosurgery
General Hospital of Tianjin Medical University

No. 54, Anshan Road, Heping District

300052 Tianjin

China

Email: tjpns@yahoo.com.cn