DOUBKOVÁ, Martina, Zdeněk ADAM, Michael DOUBEK, Teodor HORVÁTH, Luděk POUR, Z. ŘEHÁK, Renata KOUKALOVÁ and Zdeněk KRÁL. Diagnostika a léčba plicní formy histiocytózy z langerhansových buněk (Diagnosis and treatment of pulmonary Langerhans cell histiocytosis). Studia pneumologica et phtiseologica. Praha: Trios, s.r.o., 2020, vol. 80, No 2, p. 70-75. ISSN 1213-810X.
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Basic information
Original name Diagnostika a léčba plicní formy histiocytózy z langerhansových buněk
Name (in English) Diagnosis and treatment of pulmonary Langerhans cell histiocytosis
Authors DOUBKOVÁ, Martina (203 Czech Republic, guarantor, belonging to the institution), Zdeněk ADAM (203 Czech Republic, belonging to the institution), Michael DOUBEK (203 Czech Republic, belonging to the institution), Teodor HORVÁTH (203 Czech Republic, belonging to the institution), Luděk POUR (203 Czech Republic, belonging to the institution), Z. ŘEHÁK (203 Czech Republic), Renata KOUKALOVÁ (203 Czech Republic) and Zdeněk KRÁL (203 Czech Republic, belonging to the institution).
Edition Studia pneumologica et phtiseologica, Praha, Trios, s.r.o. 2020, 1213-810X.
Other information
Original language Czech
Type of outcome Article in a journal
Field of Study 30203 Respiratory systems
Country of publisher Czech Republic
Confidentiality degree is not subject to a state or trade secret
WWW web
RIV identification code RIV/00216224:14110/20:00116631
Organization unit Faculty of Medicine
Keywords (in Czech) Langerhans cell histiocytosis smoking genes cladribine vinblastine
Keywords in English Langerhans cell histiocytosis smoking genes cladribine vinblastine
Tags rivok
Tags Reviewed
Changed by Changed by: Mgr. Tereza Miškechová, učo 341652. Changed: 8/4/2021 07:57.
Abstract
Pulmonary Langerhans cell histiiocystosis is a rare discorder that occurs minly in young smokers. i is characterized by proliferation and infiltration of Langerhans cells in the lungs. The etiology is unknown, but in some cases, mutations i the BRAF or NRAS, KRAS and MAP2K1 genes may be found. The disease may resolve spntaneusly or require systemic corticosteroid or cytostatic druh therapy. The authors present their experience with the disease and also provide X-ray documentation.
Abstract (in English)
Pulmonary Langerhans cell histiiocystosis is a rare discorder that occurs minly in young smokers. i is characterized by proliferation and infiltration of Langerhans cells in the lungs. The etiology is unknown, but in some cases, mutations i the BRAF or NRAS, KRAS and MAP2K1 genes may be found. The disease may resolve spntaneusly or require systemic corticosteroid or cytostatic druh therapy. The authors present their experience with the disease and also provide X-ray documentation.
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