[Autoimmune cholangitis or seronegative biliary cirrhosis: report of one case].

Dakar medical Pub Date : 2008-01-01
S Ndongo, M Mbengue, D Dia, S M Seck, M M Ka, T Moreira Diop
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引用次数: 0

Abstract

Introduction: Auto-immune cholangitis appears by a table of cholestatic jaundice without anomalies of the hepatic bile ducts. It is a primitive biliary cirrhosis without antimitochondrial antibodies. This disease is reported at adult women in 90 % of cases. We report a 59 years old man case.

Observation: The patient was admitted for a diffuse melanodermy, a physical asthenia and a slimming which preceded 4 months by a pruritus with cholestatic jaundice. Biology showed a normal rate of transaminase. Alkaline phosphatases and direct bilirubine were high. Hepatitis (B and C) and HIV serologies were negative. Abdominal ultrasound showed a homogeneous liver. There were no dilations of the bile ducts. Antimitochondrial antibodies were negative and the histological examination confirms diagnosis.

Conclusion: Progress was good with ursodesoxycholic acid even if interval is short (5 months of evolution).

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自身免疫性胆管炎或血清阴性胆汁性肝硬化1例报告
自身免疫性胆管炎表现为胆汁淤积性黄疸,无肝胆管异常。无抗线粒体抗体的原发性胆汁性肝硬化。据报道,90%的病例为成年妇女。我们报告一个59岁的男性病例。观察:患者因弥漫性黑色素瘤、身体虚弱和消瘦入院,4个月前出现瘙痒伴胆汁淤积性黄疸。生物学显示转氨酶正常。碱性磷酸酶和直接胆红素高。乙型、丙型肝炎和HIV血清学均为阴性。腹部超声显示肝脏均匀。胆管未见扩张。抗线粒体抗体阴性,组织学检查证实诊断。结论:熊去氧胆酸治疗即使间隔时间短(5个月),进展良好。
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