Rare childhood hybrid histiocytosis of the central nervous system-diagnosed by stereotactic brain biopsy with marked treatment response to clofarabine

J Foss-Skiftesvik, D Scheie, C Klausen, A Sehested, J Skjøth-Rasmussen

2 Citationer (Scopus)

Abstract

Histiocytosis is a heterogeneous group of disease entities, comprised by two main categories, namely Langerhans and non-Langerhans cell histiocytoses. Central nervous system involvement in histiocytosis is considered very rare and is often secondary to affection of anatomically related bone structures and/or multi-organ disease. We present a never-before described case of rare childhood histiocytosis with hybrid features of Langerhans cell histiocytosis and juvenile xanthogranuloma confined to the central nervous system in a 2- and a half-year-old boy with distinct treatment response to clofarabine. The case also emphasizes the diagnostic significance of stereotactic brain biopsy.

OriginalsprogEngelsk
TidsskriftChild's Nervous System
Vol/bind34
Udgave nummer11
Sider (fra-til)2321-2324
Antal sider4
ISSN0256-7040
DOI
StatusUdgivet - 1 nov. 2018

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