Langerhan's Cell Histiocytosis Masquerading as Intertrigo
نویسندگان
چکیده
منابع مشابه
Infantile Scabies Masquerading as Langerhans Cell Histiocytosis
Vol. 27, No. 3, 2015 349 Received January 10, 2014, Revised July 7, 2014, Accepted for publication July 30, 2014 Corresponding author: Chun Wook Park, Department of Dermatology, Hallym University Kangnam Sacred Heart Hospital, 1 Singil-ro, Yeongdeungpo-gu, Seoul 150-950, Korea. Tel: 82-2-829-5221, Fax: 82-2-832-3237, E-mail: [email protected] This is an Open Access article distributed under th...
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Langerhans cell histiocytosis (LCH), also designated as histiocytosis-X or eosinophilic granuloma, is an uncommon dendritic cell disorder characterized by the infiltration of abnormally proliferating Langerhans cells into 1 or more organs.1 The clinical presentation of LCH varies depending on the site(s) of involvement and aggressiveness of disease. In children, it may present as LettererSiwe d...
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Introduction: Langerhans cell histiocytosis (LCH), which was previously known as histiocytosis X, refers to a group of lesions that stimulate uncontrolled proliferation of cells. The purpose of this case was to report and describe a LCH case with mandibular bone involvement in a 2.5-year-old boy. Case reports: A 2.5 years old boy with LCH of mandibular jaw who has been treated by surgical inter...
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Langerhans cell histiocytosis (LCH) is a rare disorder described as three different entities including eosinophilic granulomaof bone, the Hand-Schuller-Christian syndrome, and Letterer-Siwe disease. LCH is currently classified into singlesystem LCH, and multisystem LCH. Patients with single system LCH have an excellent prognosis, and are mostlytreated with local therapy. Multisystem LCH is subd...
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ژورنال
عنوان ژورنال: SKIN The Journal of Cutaneous Medicine
سال: 2019
ISSN: 2574-1624
DOI: 10.25251/skin.3.1.9