Cryptogenic cirrhosis in relapsing polychondritis

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Cryptogenic cirrhosis in relapsing polychondritis.

Though the first documented case was described by Jaksch-Wartenhorst (1923), the name 'relapsing polychondritis' was suggested by Pearson, Kline and Newcomer as late as 1960. The extreme rarity of the condition and its possible confusion with other common conditions in Bangladesh, for example, leprosy, gout and pyogenic conditions of the pinna prompted us to report this case. In addition, the p...

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RELAPSING POLYCHONDRITIS Biologics in Relapsing Polychondritis: A Literature Review

Background: There is no standardized therapeutic protocol for relapsing polychondritis (RP). Emergence of biologics holds much hope in the management of this connective tissue disease. Objectives: To evaluate the efficacy and safety of biologics in patients with active RP. Methods: A systematic review of the literature using PubMed was performed through December 2010. MeSH terms and keywords we...

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Relapsing polychondritis.

Relapsing polychondritis, an uncommon, chronic, multisystem disorder characterized by recurrent episodes of inflammation of cartilaginous tissues, can be life-threatening, debilitating, and difficult to diagnose. This review is based on the authors' experience with 36 patients with relapsing polychondritis who were followed from 1980 to 1997, 30 patients located elsewhere who completed a detail...

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Relapsing Polychondritis

Relapsing polychondritis (RP) is a rare systemic disease characterized by recurrent, widespread chondritis of the auricular, nasal, and tracheal cartilages. Additional clinical features include audiovestibular dysfunction, ocular inflammation, vasculitis, myocarditis, and nonerosive arthritis. Although the cause remains unknown, the etiology is suspected to be autoimmune. We describe a case of ...

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Relapsing polychondritis.

Relapsing polychondritis (RPC) is a unique and rarely observed autoimmune condition regarded as recurrent extensive chondritis of the auricular, nasal, and tracheal cartilages. Moreover, heart, main arteries, skin, and eyes may be involved. Several forms of clinical manifestations may be seen, and the pathogenesis still remains anonymous. A concomitant disease, particularly myelodysplasia or ot...

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ژورنال

عنوان ژورنال: Postgraduate Medical Journal

سال: 1983

ISSN: 0032-5473

DOI: 10.1136/pgmj.59.690.260