Results 71 to 80 of about 5,574,084 (164)
Langerhans cell histiocytosis presented as bilateral otitis media and mastoiditis
Langerhans cell histiocytosis (LCH) is a rare disease that may affect multiple organs. The etiology of LCH remains unclear to date. It is currently believed that clonal accumulation and proliferation of CD1a-positive Langerhans cells are causative.
Charalampos E Skoulakis +5 more
doaj
Langerhans cell histiocytosis (LCH) is rare unique disorder of the reticuloendothelial system characterized by an abnormal proliferation of histiocytes and eosinophilic leukocytes.
S Jayachandran, N Balaji
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Langerhans cell histiocytosis: A rare cause of pathological rib fracture
Langerhans cell histiocytosis, formerly known as histiocytosis X, represents clonal proliferations of the antigen-presenting dendritic cells, which are normally found in many organs. It is a rare disease which tends to affect children and adolescents. In
Yolcu A. +3 more
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Langerhans cell histiocytosis with pulmonary involvement and unilateral pneumothorax
Langerhans cell histiocytosis (LCH) is a rare disorder of Langerhans cell with unknown etiology, which can uncommonly be associated with pneumothorax.
Ghamartaj Khanbabaee +5 more
doaj
Diagnostic evaluation of thyroid involvement by histiocytosis X.
We report the successful diagnosis of thyroid involvement by histiocytosis X due to accurate evaluation of nuclear medicine results. METHODS: A total thyroidectomy specimen from our patient was initially suggestive of medullary thyroid carcinoma. However,
LUPOLI, GIOVANNI +6 more
core
Langerhans cell histiocytosis of the hip in children
Eight year old girl was referred to our consultation for a lameness with a flessum of the left hip with fever (38.5,C). Biology showed an inflammatory syndroma (CRP: 29 mg/l).
Zied Jlalia, Dhia Kaffel
doaj +1 more source
Background: Langerhan's cell histiocytosis (LCH), previously known as histiocytosis X, is a reactive proliferative dendritic cells of unknown pathogenesis characterized by the proliferation of Langerhan's cells and is extremely rare in the lumbar spines ...
Rully H Dahlan +6 more
doaj +1 more source
Acute disseminated histiocytosis-X: in situ immunophenotyping with monoclonal antibodies
The proliferating skin cells in a case of acute disseminated histiocytosis-X (Abt-Letterer-Siwe disease) confirmed by electron microscopy, were characterized by a panel of monoclonal antibodies using an immunoperoxidase technique.
Sillevis Smitt, J. H. +5 more
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Adult onset asynchronous multifocal eosinophilic granuloma of bone: an 11-year follow-up
Multifocal eosinophilic granuloma (EG) is a rare observation within the spectrum of histiocytosis X, generally described in children. We report the case of a 33-year-old man with multifocal EG showing an asynchronous evolution of bone lesions during a ...
Benjamin Dallaudière +4 more
doaj +1 more source

