Results 81 to 90 of about 14,672 (261)

A CASE OF HISTIOCYTOSIS IN THE PATIENT SUSPECTED TO HAVE PULMONARY TUBERCULOSIS

open access: yesТуберкулез и болезни лёгких, 2019
The article describes the clinical case of Langerhans cell histiocytosis with lesions in lungs and flat bones in a 40-year-old smoker. During 4 years, all stages of the disease were followed.
M. A. Karnaushkina   +2 more
doaj   +1 more source

Treatment of Xanthoma disseminatum – a systematic literature review

open access: yesJDDG: Journal der Deutschen Dermatologischen Gesellschaft, Volume 23, Issue 9, Page 1061-1069, September 2025.
Summary Xanthoma disseminatum is a rare disease from the spectrum of non‐Langerhans cell histiocytoses, which can be categorized into three types and is sometimes associated with systemic involvement. Due to the its rarity, there are no standardized treatment guidelines for this disease, making treatment in everyday clinical practice more difficult ...
Inga Hansen‐Abeck   +4 more
wiley   +1 more source

Letterer–Siwe Disease (LSD): A Case Report

open access: yesSudan Journal of Medical Sciences, 2018
Background: Letterer–Siwe Disease (LSD) is one of the variants of Langerhans cell histiocytosis (LCH), which is considered as a rare disease that affects many systems in the body; it is characterized by monoclonal migration and proliferation of specific ...
Suad H. H.   +3 more
doaj   +1 more source

Disseminated histiocytoses biomarkers beyond BRAFV600E: frequent expression of PD-L1. [PDF]

open access: yes, 2015
The histiocytoses are rare tumors characterized by the primary accumulation and tissue infiltration of histiocytes and dendritic cells. Identification of the activating BRAFV600E mutation in Erdheim-Chester disease (ECD) and Langerhans cell histiocytosis
Arceci, Robert J   +8 more
core   +3 more sources

Commentary: "Histiocytosis X" [PDF]

open access: yesThorax, 1998
Pulmonary Langerhans’ cell granulomatosis (LCG) is a diffuse, smoking-related lung disease characterised pathologically by bronchiolocentric inflammation, cyst formation, and widespread vascular abnormalities, and physiologically by exercise limitation. Pulmonary fibrosis is a long term sequel.
openaire   +2 more sources

High viral load of Merkel cell polyomavirus DNA sequences in Langerhans cell sarcoma tissues. [PDF]

open access: yes, 2014
International audienceBACKGROUND: Langerhans cell (LC) sarcoma (LCS) is a high-grade neoplasm with overtly malignant cytologic features and an LC phenotype.
A Kanik   +38 more
core   +4 more sources

A neonatal pustule:Langerhans cell histiocytosis [PDF]

open access: yes, 2019
Langerhans cell histiocytosis (LCH) is a rare, clinically heterogeneous disease that most commonly occurs in pediatric populations. Congenital self-limited LCH is a benign variant of LCH.
Hogeling, Marcia   +4 more
core  

Deciphering the role of Epstein-Barr virus in the pathogenesis of T and NK cell lymphoproliferations [PDF]

open access: yes, 2011
Epstein-Barr virus (EBV) is a highly successful herpesvirus, colonizing more than 90% of the adult human population worldwide, although it is also associated with various malignant diseases.
Fox, Christopher P   +2 more
core   +2 more sources

Immunotherapy of Histiocytosis-X

open access: yesHematology/Oncology Clinics of North America, 1987
This article focuses on the interaction of histiocytosis-X and the immunotherapeutic agent, suppression. Studies with this and other agents have presented us with invaluable insights into the nature of histiocytosis-X.
openaire   +2 more sources

LCH-Histiocytosis from Langerhans Cells in Craniofacial Region

open access: yesČeská Stomatologie a Praktické Zubní Lékařství, 2005
The authors retrospectively analyze the occurrence of histiocytosis from Langerhans cells (LCH) in a group of patients from the Children Stomatological Clinic in Prague - Motol from the years 1998-2003.
M. Hubáček, J. Kozák
doaj  

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