Literature DB >> 7194939

[Amyloidosis-a dreaded complication of juvenile chronic arthritis (JCA). (author's transl)].

L Schuchmann, H Michels, M Renaud, K Renz.   

Abstract

Our studies describe symptoms, clinical course and prognosis of 60 children (out of a total of 2063 patients) suffering from chronic arthritis complicated with amyloidosis. Amyloidosis is predominantly caused by the systemic subgroup of juvenile chronic arthritis, which is characterized by high inflammation activity. The amyloidosis and the sequelae are one of the main causes of death in JCA (27 of the 90 lethal cases in our juvenile chronic arthritis unit were connected with amyloidosis). Proteinuria is the most frequent sign in the early stage of the amyloidosis. Early diagnose and treatment by cytostatic drugs like chlorambucil seems to improve the prognosis. The cumulative survival results in the existence of two different subgroup of amyloidosis.

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Year:  1981        PMID: 7194939     DOI: 10.1055/s-2008-1034433

Source DB:  PubMed          Journal:  Klin Padiatr        ISSN: 0300-8630            Impact factor:   1.349


  1 in total

1.  HLA B27: a prognostic factor in juvenile chronic arthritis.

Authors:  H A Savolainen; M Lehtimäki; H Kautiainen; K Aho; P Anttila
Journal:  Clin Rheumatol       Date:  1998       Impact factor: 2.980

  1 in total

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