| Literature DB >> 20589639 |
Pascale Blouin1, Marion Yvert, Flavie Arbion, Anne Pagnier, Jean François Emile, Laurence Eitenschenck, Marie-Christine Machet, Dominique Plantaz, Philippe Colombat, Corinne Armari Alla, Jean Donadieu.
Abstract
Juvenile xanthogranuloma was diagnosed in two infants aged 8 and 2 months with skin lesions, hepatosplenomegaly, and pancytopenia. Disease control was not achieved with first-line vinblastine-steroid-VP16 combination therapy. Two courses of 2-chlorodeoxyadenosine (2CDA) (0.3 mg/kg) and cytosine arabinoside (AraC) (1 g/m(2)) were then administered for 5 days and were followed, after hematological recovery, by maintenance therapy. Both patients had normal complete blood cell counts and no signs of JXG, respectively, 31 and 24 months after diagnosis. Copyright 2010 Wiley-Liss, Inc.Entities:
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Year: 2010 PMID: 20589639 DOI: 10.1002/pbc.22629
Source DB: PubMed Journal: Pediatr Blood Cancer ISSN: 1545-5009 Impact factor: 3.167