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Juvenile xanthogranuloma: challenges in complicated cases.

Authors :
Sivapirabu G
Sugo E
Wargon O
Source :
The Australasian journal of dermatology [Australas J Dermatol] 2011 Nov; Vol. 52 (4), pp. 284-7. Date of Electronic Publication: 2011 Jul 28.
Publication Year :
2011

Abstract

Juvenile xanthogranuloma (JXG) is one of the most common forms of non-Langerhans cell histiocytosis in children. Although it usually presents as a self-limited skin lesion with typical histopathology, JXG can be challenging to diagnose due to an atypical initial presentation with corresponding variable histopathology for different stages of development. We present challenging cases of JXG from Sydney Children's Hospital, collected over 10 years - two with multisystem involvement and concomitant urticaria, one associated with neurofibromatosis, and one case of giant JXG with an initial histopathological challenge. Although JXG has been reported with urticaria pigmentosa, in two of our cases persistent urticaria, in association with JXG is discussed.<br /> (© 2011 The Authors; Australasian Journal of Dermatology © 2011 The Australasian College of Dermatologists.)

Details

Language :
English
ISSN :
1440-0960
Volume :
52
Issue :
4
Database :
MEDLINE
Journal :
The Australasian journal of dermatology
Publication Type :
Academic Journal
Accession number :
22070704
Full Text :
https://doi.org/10.1111/j.1440-0960.2011.00799.x