Results 61 to 70 of about 5,574,084 (164)

The clinicopathological characteristics and differential diagnosis of histiocytosis

open access: yesChinese Journal of Contemporary Neurology and Neurosurgery, 2015
The histiocytosis is divided into Langerhans' cell histiocytosis (histiocytosis X) and non-Langerhans' cell histiocytosis (NLCH). The former mainly occurs in lymphatic hematopoietic tissue and often involves central nervous system (CNS).
Shi-zhu YU
doaj  

Pulmonary Langerhans Cell Hysiocytosis: A Rare Pathology in The Practice of a Pulmonologist

open access: yesАрхивъ внутренней медицины
Pulmonary Langerhans cell histiocytosis is a rare disease with insidious onset and nonspecific manifestations. The article discusses two clinical cases of patients with a rare pathology — pulmonary histiocytosis from Langerhans cells.
E. S. Rvanina, N. A. Karoli
doaj   +1 more source

Bone: Histiocytosis X

open access: yes, 1900
Histiocytosis ...
MUSC Department of Pathology and Laboratory Medicine
core  

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

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

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

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  

Langerhans cell histiocytosis in children: a case report and brief review of the literature

open access: yesPAMJ Clinical Medicine, 2019
Langerhans cell histiocytosis (LCH), formerly known as histiocytosis X, is a non-malignant disease involving clonal proliferation of Langerhans cells. It is an orphan disease affecting mainly the child and the young adult.
Zakaria El Ouali   +7 more
doaj   +1 more source

Langerhans cell sarcoma of the skin in association with superficial atypical Langerhans cell proliferation

open access: yesRare Tumors, 2017
Langerhans cell sarcoma of the skin is a rare tumor with aggressive behavior. There are reports of Langerhans cell sarcoma involving the skin in patients with underlying systemic Langerhans cell histiocytosis.
Alejandro Peralta Soler   +2 more
doaj   +1 more source

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

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