Results 291 to 300 of about 25,153 (346)
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Clinical Nuclear Medicine, 2019
A 64-year-old man was treated with multiagent chemotherapy owing to high-grade non-Hodgkin lymphoma presenting as a bulky disease involving the spleen.
N. Hod +5 more
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A 64-year-old man was treated with multiagent chemotherapy owing to high-grade non-Hodgkin lymphoma presenting as a bulky disease involving the spleen.
N. Hod +5 more
semanticscholar +1 more source
T cell/histiocyte-rich large B-cell lymphoma: an update on its biology and classification
Virchows Archiv Fur Pathologische Anatomie Und Physiologie Und Fur Klinische Medizin, 2011Thomas Tousseyn
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Histopathology, 1980
Two cases of histiocytic endometritis are described, both characterized by total replacement of the endometrium with sheets of lipid‐containing histiocytic cells. This condition appears to be a rare complication of cervical occlusion and it is suggested that the histiocytic reaction occurs as a response to a haematometra.
C H, Buckley, H, Fox
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Two cases of histiocytic endometritis are described, both characterized by total replacement of the endometrium with sheets of lipid‐containing histiocytic cells. This condition appears to be a rare complication of cervical occlusion and it is suggested that the histiocytic reaction occurs as a response to a haematometra.
C H, Buckley, H, Fox
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CD19-directed CART therapy for T-cell/histiocyte–rich large B-cell lymphoma
Blood AdvancesKey Points • The 2-year progression-free survival of 58 patients with T-cell/histiocyte–rich large B-cell lymphoma treated with CD19-CART therapy was 29%.
P. Pophali +18 more
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Dermatologic Clinics, 1989
The histiocytic syndromes are currently divided into two major categories: Langerhans cell histiocytosis and non-Langerhans cell histiocytosis. The disease entities recognized under these categories are discussed. The discussion includes clinical features, histopathology, and treatment.
S S, Raimer, E, Hollabaugh
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The histiocytic syndromes are currently divided into two major categories: Langerhans cell histiocytosis and non-Langerhans cell histiocytosis. The disease entities recognized under these categories are discussed. The discussion includes clinical features, histopathology, and treatment.
S S, Raimer, E, Hollabaugh
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Cutaneous true histiocytic malignancy: True histiocytic lymphoma
Journal of the American Academy of Dermatology, 2004True histiocytic malignancies (THM) are controversial disorders that are being re-evaluated with modern cellular and molecular biology techniques. True histiocytic lymphoma (THL) is a low-incidence, poor-prognosis THM. It mainly affects the skin, gastrointestinal tract, and bone tissues.
Myriam, Chaín +7 more
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Langerhans Cell Histiocytosis: A Review of the Current Recommendations of the Histiocyte Society
Pediatric Dermatology, 2008E. Satter, W. High
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Histiocytic medullary reticulosis
The American Journal of Medicine, 1961Abstract The case presented fulfills the clinical and morphologic requirements of histiocytic medullary reticulosis as laid down by Bodley Scott and Robb-Smith [1]. This invariably and apparently rapidly fatal disease of adults is characterized morphologically by a diffuse proliferation of phagocytic histiocytes and their precursors in lymph nodes ...
F G, ZAK, E, RUBIN
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