Autoimmune hepatitis-primary biliary cirrhosis overlap syndrome concomitant with immune hemolytic anemia and immune thrombocytopenic purpura (Evans syndrome)

被引:11
作者
Korkmaz, Huseyin [1 ]
Bugdaci, Mehmet Sait [2 ]
Temel, Tuncer [3 ]
Dagli, Mehmet [4 ]
Karabagli, Pinar [5 ]
机构
[1] Selcuk Univ, Selcuklu Med Fac, Dept Internal Med, Div Gastroenterohepatol, TR-42075 Selcuklu, Konya, Turkey
[2] Konya Educ & Res Hosp, Gastroenterohepatol Clin, Meram, Konya, Turkey
[3] Osmangazi Univ, Fac Med, Dept Internal Med, Div Gastroenterol, Eskisehir, Turkey
[4] Selcuk Univ, Selcuklu Med Fac, Dept Internal Med, Div Hematol, TR-42075 Selcuklu, Konya, Turkey
[5] Selcuk Univ, Selcuklu Med Fac, Dept Pathol, TR-42075 Selcuklu, Konya, Turkey
关键词
FREQUENCY; DIAGNOSIS; FORM; PBC;
D O I
10.1016/j.clinre.2012.11.001
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Autoimmune hepatitis (AIH) and primary biliary cirrhosis (PBC) associated with Evans syndrome; combination of autoimmune hemolytic anemia (AIHA) and immune thrombocytopenic purpura (ITP) has rarely been reported. We report the case of a 53-year-old patient who presented with weakness, myalgia, arthralgia, shortness of breath and purpura. Initial laboratory investigations revealed liver dysfunction, anemia and thrombocytopenia. Anti-nuclear (ANA) and antimitochondrial M2 (AMA M2) antibodies were positive. Diagnose of PBC-AIH overlap was made by clinical, serological and histological investigations. AIHA and ITP was identified with clinical-laboratory findings and bone marrow puncture. She was treated with IVIG followed by prednisolone and ursodeoxycholic acid. Hemoglobin-thrombocytes increased rapidly and transaminases improved at day 8. We have reported the first case in the literature with AIH-PBC overlap syndrome concurrent by ITP and AIHA which suggest the presence of shared genetic susceptibility factors in multiple autoimmune conditions including AIH, PBC, ITP and AIHA. (C) 2012 Elsevier Masson SAS. All rights reserved.
引用
收藏
页码:E45 / E50
页数:6
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