Results 11 to 20 of about 53,392 (307)

Langerhans' cell histiocytosis in adults [PDF]

open access: bronzeJournal of the American Academy of Dermatology, 1997
Three cases of Langerhans' cell histiocytosis with unusual clinical and histopathologic features are described. The first two cases illustrate diagnostic pitfalls that underscore the importance of considering Langerhans' cell histiocytosis in the differential diagnosis of purpuric papular eruptions of the scalp and intertriginous areas, particularly in
Fiorina Giona   +9 more
openalex   +4 more sources

Langerhans cell histiocytosis

open access: yesКлинический разбор в общей медицине, 2023
Langerhans cell histiocytosis is a rare proliferative disease of histiocyte-like cells, the peak incidence of which occurs in early childhood. Pulmonary Langerhans Cell Histiocytosis is one of the forms of this disease, but it usually affects young ...
Victor V. Fomin   +4 more
doaj   +2 more sources

Polyostotic Langerhans cell histiocytosis presenting as halitosis in a 24-year-old man: a case report [PDF]

open access: yesJournal of Medical Case Reports
Background Langerhans cell histiocytosis is a rare disease of the reticuloendothelial system. This report presents a novel case of Langerhans cell histiocytosis with systemic involvement that started with a simple chief complaint.
Hassan Mirmohammad Sadeghi   +6 more
doaj   +2 more sources

Langerhans cell histiocytosis [PDF]

open access: bronzeBritish Journal of Haematology, 2000
Richard D. Brunning
openalex   +4 more sources

Insights into etiology and management of a case of Langerhans cell histiocytosis manifesting as perianal lesions: a case report [PDF]

open access: yesJournal of Medical Case Reports
Background Langerhans cell histiocytosis is a rare disorder characterized by abnormal proliferation of Langerhans cells, primarily affecting children and occasionally adults.
Pei Xiao-yue, Tai Zixin, Zhang Wen-jun
doaj   +2 more sources

Differentiation of Langerhans cells in Langerhans cell histiocytosis

open access: bronzeBlood, 2001
Langerhans cell histiocytosis (LCH) consists of lesions composed of cells with a dendritic Langerhans cell (LC) phenotype. The clinical course of LCH ranges from spontaneous resolution to a chronic and sometimes lethal disease. We studied 25 patients with various clinical forms of the disease.
Frédéric Geissmann   +8 more
openalex   +4 more sources

International expert consensus recommendations for the diagnosis and treatment of Langerhans cell histiocytosis in adults

open access: yesBlood, 2022
Langerhans cell histiocytosis (LCH) can affect children and adults with a wide variety of clinical manifestations, including unifocal, single-system multifocal, single-system pulmonary (smoking-associated), or multisystem disease.
G. Goyal   +17 more
semanticscholar   +1 more source

Langerhans cell histiocytosis: Version 2021

open access: yesHematological Oncology, 2021
Children with Langerhnans cell histiocytosis (LCH) develop granulomatous lesions with characteristic clonal CD207+ dendritic cells that can arise as single lesions or life‐threatening disseminated disease. Despite the wide range of clinical presentations,
N. Gulati, C. Allen
semanticscholar   +1 more source

Treatment outcomes and prognostic factors of patients with adult Langerhans cell histiocytosis

open access: yesAmerican journal of hematology/oncology, 2021
Adult Langerhans cell histiocytosis (LCH) remains poorly defined. We retrospectively studied 266 newly diagnosed LCH patients to understand the clinical presentation, treatment, and prognosis of adult LCH. The median age at diagnosis was 32 years (range,
Xin-xin Cao   +12 more
semanticscholar   +1 more source

Establishment of MOS-SF36 percentile ranks in the general youth French population

open access: yesBMC Psychology, 2022
Background The SF-36 is a generic quality of life questionnaire, massively translated and widely used to obtain physical and mental health status. However, validation work in the French language was carried out over a generation ago.
Arthur Trognon   +4 more
doaj   +1 more source

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