Langerhans cell granulomatosis
Authors:
J. Homolka 1, 2; I. Haškovcová 3
Authors‘ workplace:
I. klinika tuberkulózy a respiračních nemocí 1. lékařské fakulty UK a VFN Praha, přednosta prof. MU Dr. Jiří Homolka, DrSc.
1; Pneumologická klinika 1. lékařské fakulty UK a FTN Praha, přednosta prof. MU Dr. Jiří Homolka, DrSc.
2; Ústav patologie 1. lékařské fakulty UK a VFN Praha, přednosta prof. MU Dr. Ctibor Povýšil, DrSc.
3
Published in:
Vnitř Lék 2010; 56(Supplementum 2): 74-75
Category:
Langerhans cell histiocytosis and some other Hematology rare diseases
Overview
Langerhans cell granulomatosis is a rare disease of unknown aetiology and characterized by an infiltration of alveolar septa with activated Langerhans cells and eosinophylic granulocytes. Accumulation of these cells leads to a development of multiple cystic formations. The involvement of the lungs is usually present on its own, more rarely it is seen as part of a systemic disease involving skeleton or posterior pituitary. The disease prognosis in adult patients is usually good, 80% of patients achieve remission or stabilization of the disease either spontaneously or following a corticosteroid therapy, 10 – 20% of cases progress to respiratory failure.
Key words:
Langerhans cell granulomatosis – diagnostics – BAL – treatment
Sources
1. Homolka J, Křepelka J, Velenská Z. Záměna histiocytózy X za kryptogenní fibrotizující alveolitidu. Prakt Lék 1991; 71 : 20 – 22.
2. Kodet R, Zítková M. Morfologické a rentgenové plicní nálezy při disseminované histiocytóze X. Čs Pediat 1985; 40 : 634 – 638.
3. Moore AD, Godwin JD, Müller NL et al. Pulmonary histiocytosis X: comparison of radiographic and CT findings. Radiology 1989; 172 : 249 – 254.
4. Skácel Z, Marel M, Vraštilová P et al. Histiocytóza z Langerhansových buněk. Stud Pneumol Phthiseol 2000; 60 : 150 – 156.
5. Tazi A. Adult pulmonary Langerhans’ cell histiocytosis. Eur Respir J 2006; 27 : 1272 – 1285.
6. Yağci B, Varan A, Cağlar M et al. Langerhans cell histiocytosis: retrospective analysis of 217 cases in a single center. Pediatr Hematol Oncol 2008; 25 : 399 – 408.
7. Zeppa P, Cozzolino I, Russo M et al. Pulmonary Langerhans cell histiocytosis (histiocytosis X) on bronchoalveolar lavage: a report of 2 cases. Acta Cytol 2007; 51 : 480 – 482.
Labels
Diabetology Endocrinology Internal medicineArticle was published in
Internal Medicine

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