Hypercalcaemia and angioimmunoblastic lymphadenopathy.
نویسندگان
چکیده
منابع مشابه
Hypercalcaemia and angioimmunoblastic lymphadenopathy
A 57-year-old woman presented in November 1978 with a two-month history of intermittent fever, an evanescent non-pruritic rash, loss of 10 kg, and generalised lymphadenopathy and hepatosplenomegaly. Haemoglobin concentration was 7 8 g/dl, white cell count 316 x 109/1 (31 600/mm3), and platelet count 142 x 109/1. Erythrocyte sedimentation rate was 102 mm in first hour (Westergren), and Coombs te...
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Angioimmunoblastic lymphadenopathy (AILD) is a lymphoproliferative disorder with well established clinical and histological features, one of the clinical manifestations being a peripheral polyarthritis. A case of AILD with a symmetrical non-erosive peripheral polyarthritis is described, including the findings in the synovial fluid and histology of the synovium. There was a marked reduction in t...
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We report 2 contrasting cases of a seronegative polyarthritis associated with angioimmunoblastic lymphadenopathy (AILD). Both cases were nonerosive, with symmetrical involvement of the elbows, wrists, knees, and ankles. In one the arthritis appeared concurrently with the main systemic manifestations of AILD. The second presented with polyarthritis 18 months before the onset of AILD. This patien...
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Angioimmunoblastic lymphadenopathy occurred in a 46-year-old man 16 months after an episode of infectious mononucleosis induced by Epstein-Barr (EB) virus. The features of infectious mononucleosis included fever, pharyngitis, lymph gland enlargement, hepatosplenomegaly, hyperbasophilic mononuclear cells, and IgM antibodies to EB virus, although heterophile antibodies were not detected. The illn...
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ژورنال
عنوان ژورنال: BMJ
سال: 1981
ISSN: 0959-8138,1468-5833
DOI: 10.1136/bmj.282.6262.437