Literature DB >> 12856748

Successful treatment of Langerhans cell histiocytosis with 2-chlorodeoxyadenosine.

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.

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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


  5 in total

Review 1.  Rare lung diseases III: pulmonary Langerhans' cell histiocytosis.

Authors:  Stephen C Juvet; David Hwang; Gregory P Downey
Journal:  Can Respir J       Date:  2010 May-Jun       Impact factor: 2.409

Review 2.  Langerhans cell histiocytosis.

Authors:  Kevin Bradford Hoover; Daniel I Rosenthal; Henry Mankin
Journal:  Skeletal Radiol       Date:  2006-10-07       Impact factor: 2.128

Review 3.  Pulmonary langerhans cell histiocytosis.

Authors:  Harpreet S Suri; Eunhee S Yi; Gregorz S Nowakowski; Robert Vassallo
Journal:  Orphanet J Rare Dis       Date:  2012-03-19       Impact factor: 4.123

4.  2-Chlorodeoxyadenosine treatment for cutaneous T-cell lymphoma.

Authors:  Małgorzata Sokołowska-Wojdyło; Magdalena Trzeciak; Jadwiga Roszkiewicz
Journal:  Dermatol Reports       Date:  2010-09-02

5.  Effectiveness of cladribine therapy in patients with pulmonary Langerhans cell histiocytosis.

Authors:  Vincent Grobost; Chahera Khouatra; Romain Lazor; Jean-François Cordier; Vincent Cottin
Journal:  Orphanet J Rare Dis       Date:  2014-11-30       Impact factor: 4.123

  5 in total

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