Angioimmunoblastic lymphadenopathy associated with polyarthritis.

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منابع مشابه

Polyarthritis and angioimmunoblastic lymphadenopathy.

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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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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Arthritis and angioimmunoblastic lymphadenopathy.

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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Haematological features of angioimmunoblastic lymphadenopathy with dysproteinaemia.

A study of seven patients with AILD has confirmed previously reported cytological and immunological changes in the peripheral blood. In themselves these changes should not be considered as specific. Histological examination of the bone marrow may show more characteristic lesions which involve haemopoietic, lymphoid, and stromal cells. Three patients had bone marrow features similar to myelofibr...

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Peripheral neuropathy in angioimmunoblastic lymphadenopathy with dysproteinaemia.

A case of angioimmunoblastic lymphadenopathy with dysproteinaemia complicated by a subacute peripheral neuropathy is described. Clinically the neuropathy was mainly motor, but pain and paraesthesiae in the legs were also present. Sural nerve biopsy indicated decreased numbers of myelinated fibres, mainly the largest, without actual signs of degeneration or regeneration. However, the occurrence...

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ژورنال

عنوان ژورنال: Annals of the Rheumatic Diseases

سال: 1980

ISSN: 0003-4967

DOI: 10.1136/ard.39.4.406