Results 81 to 90 of about 1,944 (124)
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ANGIO-IMMUNOBLASTIC LYMPHADENOPATHY WITH DYSPROTEINÆMIA
Lancet, The, 1974Abstract A new disease with a lymphoma-like Summary clinical presentation and a specific histological picture has been recognised in fifteen patients. Clinically, the disease, which seems to occur chiefly in the elderly, is characterised by an acute onset of constitutional symptoms, generalised lymphadenopathy, hepatosplenomegaly, and ...
C H Horne, J C Petrie
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Angio-Immunoblastic (Immunoblastic) Lymphadenopathy
New England Journal of Medicine, 1975The clinical picture of generalized lymphadenopathy with or without hepatosplenomegaly may be seen in a variety of diseases.
H Rappaport
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The Lung in Immunoblastic Lymphadenopathy
Chest, 1981Immunoblastic lymphadenopathy presents with fever, malaise, cough, dyspnea, lymphadenopathy, hepatosplenomegaly, hypergammaglobulinemia, interstitial pulmonary infiltrates, mediastinal adenopathy, and effusions. The diagnosis is made on the basis of lymph node biopsy.
S L, Bradley +3 more
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Immunoblastic lymphadenopathy and asbestosis
Cancer, 1981Immunoblastic lymphadenopathy was diagnosed in a 71-year-old white man who had weakness, with weight loss, fever, cough, and generalized lymphadenopathy. The patient had a long occupational history of shipyard work. Diagnosis of asbestosis was made clinically by chest x-ray, and ferruginous bodies were found in the lung at autopsy.
F W, Maguire, R C, Mills, F P, Parker
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IMMUNOBLASTIC LYMPHOMA IN ANGIO-IMMUNOBLASTIC LYMPHADENOPATHY
Lancet, The, 1979Marshall E Kadin
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Evolution of Angio-Immunoblastic Lymphadenopathy
New England Journal of Medicine, 1977Thomas L Perry
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Splenectomy for treatment of immunoblastic lymphadenopathy
British Journal of Haematology, 1994Summary. A 5‐month‐old girl was diagnosed with immunoblastic lymphadenopathy (IBL) on the basis of clinical symptoms and pathological findings. α‐interferon. immunosuppressive agents such as cyclosporin A, deoxyspagarine, and azathioprine, and an alternating regimen of low‐dose 6‐ mercaptopurine, cyclophosphamide and methotrexate were tried with ...
Akira Okada
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New England Journal of Medicine, 1975
Immunoblastic lymphadenopathy, although it resembles Hodgkin's disease, is a distinct, hyperimmune disorder apparently of the B-cell system. In 32 cases, it was characterized by a morphologic triad: proliferation of arborizing small vessels; prominent immunoblastic proliferations; and amorphous acidophilic interstitial material.
Robert J Lukes +2 more
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Immunoblastic lymphadenopathy, although it resembles Hodgkin's disease, is a distinct, hyperimmune disorder apparently of the B-cell system. In 32 cases, it was characterized by a morphologic triad: proliferation of arborizing small vessels; prominent immunoblastic proliferations; and amorphous acidophilic interstitial material.
Robert J Lukes +2 more
exaly +3 more sources
Amyloid deposition in immunoblastic lymphadenopathy
Human Pathology, 1978Two cases of immunoblastic lymphadenopathy are reported that in addition to having the usual histologic and electron microscopic appearance previously described exhibit perivascular and intersitial green polarization when stained with Congo red, indicating amyloid deposition.
J A, Madri, F, Fromowitz
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