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Treatment of Langerhans Cell Histiocytosis
Histiocytosis X patients present with a variety of clinical manifestations and outcomes. The principal difficulty in the establishment of a definite protocol for treatment is based on the poor understanding of the basic nature of this disease, the ...
김현우, 신규호
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Indeterminate Cell Histiocytosis in Children: A Case Report
A. Sahuquillo-Torralba +3 more
openaire +1 more source
Indeterminate cell histiocytosis (ICH) is a proliferation of indeterminate CD1a+, CD68+, S100+ and CD207- dermal dendritic cells. We describe a 39-year-old man who developed diffuse ICH and, 6 years later, acute myeloblastic leukaemia (AML). He was treated with cyclophosphamide, etoposide and vinblastine until 2003.
Emilio Berti, Umberto Gianelli
exaly +4 more sources
Indeterminate Cell Histiocytosis of the Spine: A Case Report
<b><i>Introduction:</i></b> Indeterminate cell histiocytosis is a rare neoplastic disease characterized by proliferation of dendritic cells that share morphologic and immunophenotypic features of Langerhans cells and non-Langerhans histiocytes.
Dallas Louis, Sheinberg +3 more
openaire +3 more sources
Indeterminate Cell Histiocytosis: A Rare Histiocytic Disorder
A 64-year-old woman, otherwise healthy, presented with multiple reddish-brown, slightly yellowish papules on the face and neck, which had developed 3 years earlier. The lesions were painless and nonpruritic and varied in diameter from 1 to 5 mm. Histological and immunohistochemical examination of cutaneous biopsies revealed a diffuse dermal infiltrate ...
Manente, L +7 more
openaire +4 more sources
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Indeterminate cell histiocytosis treated with 0.5% delgocitinib ointment
British Journal of Dermatology, 2023Although delgocitinib has been used for atopic dermatitis, it is also effective for indeterminate cell histiocytosis, a rare CD207–/CD1a+ histiocyte proliferative disease.
Rai F T, Fujimoto +3 more
exaly +3 more sources
A Case of Solitary Indeterminate Cell Histiocytosis
Journal of Dermatology, 2003Yasuyuki, Amo +3 more
exaly +3 more sources
Indeterminant Cell Histiocytosis in a Patient With Hemophagocytic Lymphohistiocytosis
The American Journal of Dermatopathology, 2021Abstract: Indeterminant cell histiocytosis is a rare disorder, which often presents as a benign, papular eruption without age or sex predilection. It is diagnosed based on histologic findings that are similar to those seen in Langerhans cell histiocytosis without the characteristic Birbeck granules.
Hannah S, Berman +2 more
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Tick bite mimicking indeterminate cell histiocytosis
Pediatric Dermatology, 2017AbstractTicks are a well‐known vector for viral, bacterial, and rickettsial infections, many of which are accompanied by cutaneous eruptions, but the bite itself can induce a spectrum of inflammatory reactions, including foreign body granuloma, tick bite alopecia, and cutaneous lymphoid hyperplasia.
Thomas Stringer +5 more
openaire +2 more sources
Indeterminate cell histiocytosis: fact or fiction?
Journal of Cutaneous Pathology, 2005Abstract: Indeterminate cell histiocytosis is a rare disorder, in which the predominant cells have the characteristics of both Langerhans cells and macrophages. We, in this study, describe 18 patients and compare them with those previously published. Most patients were adults with either solitary or multiple red‐brown papules or nodules.
Gudrun, Ratzinger +4 more
openaire +2 more sources

