Literature DB >> 11680268

[Reynolds syndrome: the combination of scleroderma and primary biliary cirrhosis. Case report].

B Brzezińska-Kolarz1, A Undas, A Dyczek, J Musiał.   

Abstract

A 57-year--woman with Reynolds syndrome (primary biliary cirrhosis and scleroderma) is reported. Diagnosis of primary biliary cirrhosis is based on clinical findings, laboratory tests results and histological result of liver biopsy. Scleroderma was confirmed by anticentromere antibodies presence, and typical skin lesions. Although, antimitochondrial antibodies are very typical for PBC (primary biliary cirrhosis), in this case the were not found.

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Year:  2001        PMID: 11680268

Source DB:  PubMed          Journal:  Pol Arch Med Wewn


  3 in total

1.  Clinical features and prognosis of primary biliary cirrhosis associated with systemic sclerosis.

Authors:  C Rigamonti; L M Shand; M Feudjo; C C Bunn; C M Black; C P Denton; A K Burroughs
Journal:  Gut       Date:  2005-09-08       Impact factor: 23.059

2.  Primary biliary cirrhosis associated with systemic sclerosis: diagnostic and clinical challenges.

Authors:  Cristina Rigamonti; Dimitrios P Bogdanos; Maria G Mytilinaiou; Daniel S Smyk; Eirini I Rigopoulou; Andrew K Burroughs
Journal:  Int J Rheumatol       Date:  2011-12-06

Review 3.  Towards systemic sclerosis and away from primary biliary cirrhosis: the case of PTPN22.

Authors:  Daniel S Smyk; Maria G Mytilinaiou; Piotr Milkiewicz; Eirini I Rigopoulou; Pietro Invernizzi; Dimitrios P Bogdanos
Journal:  Auto Immun Highlights       Date:  2011-09-07
  3 in total

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