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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 ...
R Maarten Egeler, P. Van Heerde
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Cancer, 1983
The clinical features, therapy, and hospital course of ten consecutive patients with malignant histiocytosis (MH) are presented. The value of bone marrow aspiration for the diagnosis is discussed. The patient's performance status as described in this report by the organ dysfunction score may predict survival and response to chemotherapy. The literature
D W, Esseltine +2 more
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The clinical features, therapy, and hospital course of ten consecutive patients with malignant histiocytosis (MH) are presented. The value of bone marrow aspiration for the diagnosis is discussed. The patient's performance status as described in this report by the organ dysfunction score may predict survival and response to chemotherapy. The literature
D W, Esseltine +2 more
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Archives of Pediatrics & Adolescent Medicine, 1971
1. The clinical, histological and radiological findings in 129 cases of histiocytosis X have been reviewed and the natural history of the disease is discussed. 2. Certain clinical and histological factors emerge as having prognostic significance. 3. The treatment in thirty-four personally reviewed cases is discussed and some suggestions are made as ...
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1. The clinical, histological and radiological findings in 129 cases of histiocytosis X have been reviewed and the natural history of the disease is discussed. 2. Certain clinical and histological factors emerge as having prognostic significance. 3. The treatment in thirty-four personally reviewed cases is discussed and some suggestions are made as ...
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Histopathology, 1994
The majority of cases of intravascular lymphomatosis are B‐cell lymphomas with only the occasional case being of T‐cell type. We report a case of intravascular lymphomatosis in which the proliferating cells were of histiocytic type; the tumour has recurred following treatment.
J T, O'Grady +3 more
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The majority of cases of intravascular lymphomatosis are B‐cell lymphomas with only the occasional case being of T‐cell type. We report a case of intravascular lymphomatosis in which the proliferating cells were of histiocytic type; the tumour has recurred following treatment.
J T, O'Grady +3 more
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Diverse kinase alterations and myeloid-associated mutations in adult histiocytosis
Leukemia, 2021Jia Chen +10 more
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Intracranial dural histiocytosis
British Journal of Neurosurgery, 2009Rosai-Dorfman disease is a common benign lymphomatous disorder that involves the lymph nodes and other solid organs. Neurological involvement is rare, and an isolated intracranial Rosai-Dorfman lesion even rarer. Whether isolated intracranial Rosai-Dorfman lesions should be defined as Rosai-Dorfman disease or intradural histiocytosis remains debatable.
Natale Russo +3 more
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2005
Publisher Summary This chapter discusses clinical manifestations, pathology, diagnostic features, and treatments of histiocytosis syndromes and other disorders. Histiocytosis syndrome identifies a group of disorders that have in common the proliferation of cells of the mononuclear phagocyte system and the dendritic cell system. Histiocytes are defined
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Publisher Summary This chapter discusses clinical manifestations, pathology, diagnostic features, and treatments of histiocytosis syndromes and other disorders. Histiocytosis syndrome identifies a group of disorders that have in common the proliferation of cells of the mononuclear phagocyte system and the dendritic cell system. Histiocytes are defined
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Current Opinion in Hematology, 2001
Until recently, malignant histiocytosis was a clearly defined clinical entity marked by fever, progressive wasting, lymphadenopathy, hepatosplenomegaly, and pancytopenia. However, for many years the morphologic findings in this disease continued to cause a great deal of controversy.
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Until recently, malignant histiocytosis was a clearly defined clinical entity marked by fever, progressive wasting, lymphadenopathy, hepatosplenomegaly, and pancytopenia. However, for many years the morphologic findings in this disease continued to cause a great deal of controversy.
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