Giant skull vault defect in a child caused by Langerhans cell histiocytosis: the “calvaria-eating disease”

Langerhans cell histiocytosis (LCH) is a rare disease of young children that can be difficult to diagnose and treat. Clinical manifestations can sometimes be quite unusual, and bony lesions can reach a large size before treatment is sought. We present a unique case of a 3-year-old male child with a...

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Bibliographic Details
Published inChild's nervous system Vol. 36; no. 3; pp. 651 - 654
Main Authors Gosal, Jaskaran Singh, Ruparelia, Jigish, Garg, Mayank, Praneeth, Kokkula, Bhaskar, Suryanarayanan, Jha, Deepak Kumar
Format Journal Article
LanguageEnglish
Published Berlin/Heidelberg Springer Berlin Heidelberg 01.03.2020
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