Results 181 to 190 of about 24,068 (238)
A Case of Primary Cutaneous BRAF<sup>V600E+</sup> Langerhans Cell Histiocytosis, With Underlying Chronic Myelomonocytic Leukaemia, Responsive to Dabrafenib With Subsequent Undetectable Circulating Cell Free DNA. [PDF]
Australas J DermatolSimpson K +6 more
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Disease extent, not lesion location, determines relapse risk in single-system skeletal Langerhans cell histiocytosis. [PDF]
Blood AdvAstigarraga I +16 more
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Hepatobiliary langerhans cell histiocytosis mimicking Caroli syndrome and recurring in a liver allograft. [PDF]
Front Med (Lausanne)Hu T, Wang C, Liu C, Sun J.
europepmc +1 more source
Annals of African Medicine, 2009 Histiocytosis X (Langerhan’s cell granulomatosis) is a disease of unknown aetiology, but viral origin has been implicated.1 It is a clinicopathologic entitycharacterized by proliferation of Langerhan’s cell (which are not primarily phagocytic) in an appropriate milieu ...
Mohammed, A. +4 more
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The Cytology of Langerhans Cell Histiocytosis (Histiocytosis X)
Cytopathology, 1991The cytomorphology of 13 cases of Langerhans cell histiocytosis is described. the most striking features were the presence of intranuclear clefts, pale nuclei and inconspicuous nucleoli, together with ample pale cytoplasm, only slight cellular pleomorphism, and an admixture of varying numbers of eosinophils, macrophages and degenerated cells.In 13 of ...
P, Van Heerde, R, Maarten Egeler
exaly +3 more sources
The Lancet, 2021
Histiocytoses constitute a heterogeneous group of rare disorders, characterised by infiltration of almost any organ by myeloid cells with diverse macrophage or dendritic cell phenotypes. Histiocytoses can start at any age. Diagnosis is based on histology in combination with appropriate clinical and radiological findings.
Emile, Jean-François +8 more
openaire +4 more sources
Histiocytoses constitute a heterogeneous group of rare disorders, characterised by infiltration of almost any organ by myeloid cells with diverse macrophage or dendritic cell phenotypes. Histiocytoses can start at any age. Diagnosis is based on histology in combination with appropriate clinical and radiological findings.
Emile, Jean-François +8 more
openaire +4 more sources
Medicina Clínica, 2023
Histiocytosis is a group of rare diseases characterized by inflammation and accumulation of cells derived from monocytes and macrophages in different tissues. The symptoms are highly variable, from mild forms with involvement of a single organ to severe multisystem forms that can be life compromising.
Gemma, Rocamora-Blanch +2 more
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Histiocytosis is a group of rare diseases characterized by inflammation and accumulation of cells derived from monocytes and macrophages in different tissues. The symptoms are highly variable, from mild forms with involvement of a single organ to severe multisystem forms that can be life compromising.
Gemma, Rocamora-Blanch +2 more
openaire +2 more sources
The Journal of Dermatology, 1988
AbstractThree patients with multiple skin nodules on the trunk and extremities showed hyperpyrexia, lymphadenopathy, pancytopenia, abnormal liver function, and terminal hemorrhagic diathesis. Histologically, the deep dermis and subcutaneous fat contained dense infiltrates of atypical erythropagocytic histiocytes and lymphoid cells.
M H, Chen +4 more
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AbstractThree patients with multiple skin nodules on the trunk and extremities showed hyperpyrexia, lymphadenopathy, pancytopenia, abnormal liver function, and terminal hemorrhagic diathesis. Histologically, the deep dermis and subcutaneous fat contained dense infiltrates of atypical erythropagocytic histiocytes and lymphoid cells.
M H, Chen +4 more
openaire +2 more sources
Otolaryngology–Head and Neck Surgery, 1980
Histiocytosis X is characterized by a proliferation of cytologically benign histiocytes and occurs in a severe form (type 1) with a short course and poor prognosis and a milder form (type 2) with a protracted course and favorable prognosis. Otolaryngologists will encounter the type 2 form of the disease and must include it in the differential diagnosis
Harold F. Schuknecht, Spyros Papaspyrou
openaire +4 more sources
Histiocytosis X is characterized by a proliferation of cytologically benign histiocytes and occurs in a severe form (type 1) with a short course and poor prognosis and a milder form (type 2) with a protracted course and favorable prognosis. Otolaryngologists will encounter the type 2 form of the disease and must include it in the differential diagnosis
Harold F. Schuknecht, Spyros Papaspyrou
openaire +4 more sources
Human Pathology, 1983
To clarify salient issues pertaining to histiocytosis X--a syndrome that includes Letterer-Siwe disease, Hand-Schuller-Christian disease, and eosinophilic granuloma--the authors review the epidemiologic data and the histologic, morphologic, and clinical bases for diagnosis and prognosis. Histiocytes are defined and their possible histogenesis outlined,
B E, Favara, R C, McCarthy, G W, Mierau
openaire +2 more sources
To clarify salient issues pertaining to histiocytosis X--a syndrome that includes Letterer-Siwe disease, Hand-Schuller-Christian disease, and eosinophilic granuloma--the authors review the epidemiologic data and the histologic, morphologic, and clinical bases for diagnosis and prognosis. Histiocytes are defined and their possible histogenesis outlined,
B E, Favara, R C, McCarthy, G W, Mierau
openaire +2 more sources