Neuropediatrics 2005; 36(5): 328-331
DOI: 10.1055/s-2005-872814
Short Communication

Georg Thieme Verlag KG Stuttgart · New York

Marchiafava-Bignami-Like Injury of the Corpus Callosum in an Infant

S. P. Toelle1 , T. A. G. M. Huisman2 , E. Martin3 , E. Boltshauser1
  • 1Department of Neurology, University Children's Hospital, Zurich, Switzerland
  • 2Department of Diagnostic Imaging, University Children's Hospital, Zurich, Switzerland
  • 3MRI‐Center, University Children's Hospital, Zurich, Switzerland
Further Information

Publication History

Received: April 22, 2005

Accepted after Revision: July 28, 2005

Publication Date:
11 October 2005 (online)

Abstract

We report on a 16-month-old boy who presented with truncal ataxia and intermittent nystagmus. Magnetic resonance imaging (MRI) at 19 months showed a T2-hyperintensity of the splenium and the genu of the corpus callosum with extension into the adjacent frontal white matter. Diffusion tensor imaging (DTI) revealed a corresponding area of restricted diffusion, suggesting cytotoxic oedema. The extent and localisation of the signal abnormalities mimic tissue injury as seen in Marchiafava-Bignami disease (MBD). Metabolic investigations were normal. Follow-up imaging at 24 months showed a similar T2-hyperintensity of the corpus callosum and white matter while on DTI the cytotoxic oedema had resolved. Clinically a remaining truncal and gait ataxia, clumsiness and a developmental delay is seen. Goal of this case report is (a) to present a rare case of Marchiafava-Bignami-like injury of the corpus callosum in an infant and (b) to discuss the neuroradiological imaging findings including MRI and DTI.

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MD Sandra Toelle

Department of Neurology
University Children's Hospital

Steinwiesstrasse 75

8032 Zürich

Switzerland

Email: sandra.toelle@kispi.unizh.ch

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