Results 21 to 30 of about 4,942,068 (276)
Clinical, Cosmetic and Investigational Dermatology, 2021 Jinjing Zhang,1 Shiyu Ma,1 Jinxiang Yu,1 Song Zheng,2 Yuan Miao,3 Pingping Wang,1 Xiaojing Yan1 1Department of Hematology, The First Affiliated Hospital of China Medical University, Shenyang, Liaoning, 110001, People’s Republic of China; 2Department of ...
Zhang J +6 more
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Hepatic Langerhans cell histiocytosis: Report of a rare case
Human Pathology Reports, 2023 Langerhans cell histiocytosis (LCH) is a rare neoplastic disease characterized by abnormal proliferation of Langerhans cells infiltrating various organs, resulting in organ dysfunction.
Renling Yao, Jun Chen, Jie Li
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Langerhans cell origin and regulation
, 2016 Copyright \ua9 2015 Wolters Kluwer Health, Inc. Purpose of review This article summarizes recent research on the ontogeny of Langerhans cells and regulation of their homeostasis in quiescent and inflamed conditions.
Milne P, Collin M
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Case Reports in Pathology, 2017 Langerhans cells are antigen presenting dendritic cells and tumours arising from these are rare. The tumours arising from these dendritic cells are divided into two categories according to a WHO classification: Langerhans cell histiocytosis and ...
Rasika Singh +3 more
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Pulmonary Langerhans cell histiocytosis causing spontaneous bilateral pneumothorax in a child
The Egyptian Journal of Internal Medicine, 2015 Bilateral pneumothorax is very rare in childhood. Moreover, if it is due to pulmonary involvement of Langerhans cell histiocytosis, it is even rarer in childhood.
Anupam Patra +3 more
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Langerhans Cell Histiocytosis in Adults: A Canadian Multicenter Case Series. [PDF]
Hematol OncolABSTRACT Langerhans cell histiocytosis (LCH) is a rare clonal myeloid neoplasm. Canadian data on clinical characteristics, molecular profile, and treatment outcomes is limited. This study aims to report the initial experience of a Canadian rare diseases program, reflecting “real‐world” diagnostic pathways, referral patterns, and treatment heterogeneity
Quon S +7 more
europepmc +2 more sources
SAGE Open Medical Case Reports, 2014 Objective: Langerhans cell histiocytosis is an unusual disorder of unknown etiology with heterogeneous clinical behaviors and variable outcomes. It can involve one or more organs or systems, but to our best knowledge, parotid glands involvement in ...
Xiaojun Yuan +4 more
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Skin-derived dendritic cells acquire and degrade the scrapie agent following in vitro exposure [PDF]
, 2005 The accumulation of the scrapie agent in lymphoid tissues following inoculation via the skin is critical for efficient neuroinvasion, but how the agent is initially transported from the skin to the draining lymph node is not known. Langerhans cells (LCs)
Hopkins, John +5 more
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Haematologica, 2008 Clinical features, brain magnetic resonance imaging findings and EDSS scores of 11 patients with neurodegenerative central nervous system Langerhans cell histiocytosis were analyzed in Japan.
Shinsaku Imashuku +13 more
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Langerhans' Cell Histiocytosis
Dermatology Online Journal, 2002 Adult onset Langerhans cell histiocytosis is uncommon. A 29 year old man is presented who developed classic cutaneous disease with severe systemic involvement. He responded completely to a two month course of thalidomide.
Mortazavi, Hessein +3 more
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