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Langerhans cell histiocytosis [PDF]
Chinese Journal of Contemporary Neurology and Neurosurgery, 2014 doi: 10.3969/j.issn.1672-6731.2014.10 ...
Xiao-ling YAN
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Journal of Investigative Dermatology, 1965 Since Langerhans (1) first described the presence of gold-positive dendritic cells in the epidermis, their nature has been an unsettled question. These cells, which morphologically resemble melanocytes, are free of pigment and are not seen when stained for melanin nor when the dopa stain is used; but they can be demonstrated with gold chloride methods.
Alvin S. Zelickson
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Langerhans cell histiocytosis [PDF]
Blood, 2020 Abstract Langerhans cell histiocytosis (LCH) is caused by clonal expansion of myeloid precursors that differentiate into CD1a+/CD207+ cells in lesions that leads to a spectrum of organ involvement and dysfunction. The pathogenic cells are defined by constitutive activation of the MAPK signaling pathway.
Carl E. Allen, Carlos Rodriguez-Galindo
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Indian Journal of Medical Research, 2018 Langerhans cell histiocytosis (LCH) formerly known as pulmonary eosinophilic granuloma is currently regarded by the World Health Organization as a clonal neoplastic proliferation of histiocytes.
Anil S Menon, Manish Kumar
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Langerhans cell histiocytosis present in a 1-day-old girl: a case report [PDF]
Journal of Medical Case ReportsBackground Langerhans cell histiocytosis is a rare condition characterized by diverse clinical manifestations, ranging from cutaneous lesions to systemic involvement.
Yang Meng
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Langerhans cell histiocytosis [PDF]
São Paulo Medical Journal, 1998 The authors present a rare case of Langerhans cell histiocytosis in a 31 year old female patient with vulvar, peri-anal and oral lesions, diabetes insipidus, pulmonary skin and bone infiltrations.
Maria de Lourdes L. F. Chauffaille +10 more
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Journal of Indian Society of Periodontology, 2011 Langerhans cell histiocytosis (LCH) is a group of rare disorders histologically characterized by the proliferation of Langerhans cells. Multiple organs and systems may be involved by the disease. Typically, there is bone involvement and, less frequently,
D R Aruna +3 more
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Клинический разбор в общей медицине, 2023 Langerhans cell histiocytosis is a rare proliferative disease of histiocyte-like cells, the peak incidence of which occurs in early childhood. Pulmonary Langerhans Cell Histiocytosis is one of the forms of this disease, but it usually affects young ...
Victor V. Fomin +4 more
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Establishment of MOS-SF36 percentile ranks in the general youth French population
BMC Psychology, 2022 Background The SF-36 is a generic quality of life questionnaire, massively translated and widely used to obtain physical and mental health status. However, validation work in the French language was carried out over a generation ago.
Arthur Trognon +4 more
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Journal of Investigative Dermatology, 1983 Langerhans cells are the bone-marrow-derived immune cells of the epidermis; they express Ia antigens and receptors for the Fc portion of IgG and complement components and are required for epidermal-cell-induced antigen-specific, syngeneic and allogeneic T-cell activitation and the generation of epidermal-cell-induced cytotoxic T cells.
Georg Stingl, Klaus Wolff
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