Literature DB >> 17675775

Adult Langerhans cell histiocytosis with independently relapsing lung and liver lesions that was successfully treated with etoposide.

Satoshi Konno1, Nubuyuki Hizawa, Tomoko Betsuyaku, Masanori Yasuo, Hiroshi Yamamoto, Tomonobu Koizumi, Masaharu Nishimura.   

Abstract

A 35-year-old man initially presented with cough and fever. Computed tomography (CT) revealed diffuse small cysts in the lung, and multiple nodules in the liver. Lung and liver biopsies revealed that pathology was consistent with Langerhans cell histiocytosis. Lung shadows increased despite cessation of smoking, whereas the liver involvement improved. After initiating treatment with prednisolone, the chest CT findings improved. However, the liver nodules started to increase while tapering prednisolone. Intravenous etoposide was started, and the liver nodules decreased markedly. The difference in the clinical course between the lung and liver lesions might have been the result of differences in the clonality of these two organs.

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Year:  2007        PMID: 17675775     DOI: 10.2169/internalmedicine.46.6433

Source DB:  PubMed          Journal:  Intern Med        ISSN: 0918-2918            Impact factor:   1.271


  2 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

2.  Extrathoracic investigation in adult patients with isolated pulmonary langerhans cell histiocytosis.

Authors:  Abdellatif Tazi; Constance de Margerie-Mellon; Laetitia Vercellino; Jean Marc Naccache; Stéphanie Fry; Stéphane Dominique; Stéphane Jouneau; Gwenaël Lorillon; Emmanuelle Bugnet; Raphael Chiron; Benoit Wallaert; Dominique Valeyre; Sylvie Chevret
Journal:  Orphanet J Rare Dis       Date:  2016-02-02       Impact factor: 4.123

  2 in total

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