Results 241 to 250 of about 42,023 (285)
Some of the next articles are maybe not open access.
Pure cutaneous histiocytosis resembling sinus histiocytosis
Clinical and Experimental Dermatology, 1988Summary A 48-year-old Lebanese man presented with a 2-year history of painless papules and nodules of the skin without any systematic involvement, lymphadenopathy, serum electrophoresis disturbance, leukocytosis or elevated erythrocyte sedimentation rate (ESR).
R, Viraben, A, Dupre, B, Gorguet
openaire +2 more sources
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 ...
openaire +4 more sources
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 ...
openaire +4 more sources
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
openaire +2 more sources
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
openaire +2 more sources
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
openaire +2 more sources
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
openaire +2 more sources
Histiocytosis X: VIII. Histiocytosis X Simulating Tuberculosis
Acta Radiologica: Oncology, 1983The findings in 9 patients with histiocytosis X localized to the spine and 7 patients with tuberculous spondylitis were compared. It was not always possible to differentiate between these two conditions without a supplementary fine needle aspiration biopsy.
P, Thommesen, N, Bartholdy, E, Bünger
openaire +2 more sources
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.
openaire +2 more sources
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.
openaire +2 more sources
2020
Abstract The histiocytoses are disorders derived from the dendritic cell and monocyte/macrophage lineages, with the classification of this group of disorders relating to the underlying cell of origin. Dendritic cell disorders—there has been much debate about the nature of these conditions, and their status as neoplastic or primary ...
openaire +2 more sources
Abstract The histiocytoses are disorders derived from the dendritic cell and monocyte/macrophage lineages, with the classification of this group of disorders relating to the underlying cell of origin. Dendritic cell disorders—there has been much debate about the nature of these conditions, and their status as neoplastic or primary ...
openaire +2 more sources