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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Published in | Child's nervous system Vol. 36; no. 3; pp. 651 - 654 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
Published |
Berlin/Heidelberg
Springer Berlin Heidelberg
01.03.2020
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Subjects | |
Online Access | Get full text |
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