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.
Original language | English |
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Journal | Child's Nervous System |
Volume | 34 |
Issue number | 11 |
Pages (from-to) | 2321-2324 |
Number of pages | 4 |
ISSN | 0256-7040 |
DOIs | |
Publication status | Published - 1 Nov 2018 |