| Literature DB >> 12856748 |
Nicole S L Goh1, Christine E McDonald, Duncan P MacGregor, Jeffrey J Pretto, Graeme N Brodie.
Abstract
Langerhans cell histiocytosis (LCH) is a rare disorder which frequently involves the lungs of affected adults. Recent evidence suggests it is a clonal neoplastic disorder. Prognosis in this disease is variable, but in its multisystem form or when associated with progressive respiratory dysfunction, prognosis is poor. Recent case reports and a phase II trial of the antimonocyte drug 2-chlorodeoxy-adenosine (2CDA) have described success in treating LCH. We used 2CDA to treat a young Australian man with LCH involving lungs and bone. A complete symptomatic remission was achieved with no evidence of recurrence some 5 years after completion of chemotherapy.Entities:
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Year: 2003 PMID: 12856748 DOI: 10.1046/j.1440-1843.2003.00427.x
Source DB: PubMed Journal: Respirology ISSN: 1323-7799 Impact factor: 6.424