Situs inversus totalis and secondary biliary cirrhosis: a case report.

Hacı Mehmet Sökmen, Kamil Ozdil, Turan Calhan, Abdurrahman Sahin, Ebubekir Senateş, Resul Kahraman, Adil Niğdelioğlu, Ebru Zemheri
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引用次数: 1

Abstract

Situs inversus totalis is is a congenital anomaly associated with various visceral abnormalities, but there is no data about the relationship between secondary biliary cirrhosis and that condition. We here present a case of a 58 year-old female with situs inversus totalis who was admitted to our clinic with extrahepatic cholestasis. After excluding all potential causes of biliary cirrhosis, secondary biliary cirrhosis was diagnosed based on the patient's history, imaging techniques, clinical and laboratory findings, besides histolopathological findings. After treatment with tauroursodeoxycholic acid, all biochemical parameters, including total/direct bilirubin, alanine aminotransferase, aspartate aminotransferase, alkaline phosphatase and gama glutamyl transferase, returned to normal ranges at the second month of the treatment. We think that this is the first case in literature that may indicate the development of secondary biliary cirrhosis in a patient with situs inversus totalis. In conclusion, situs inversus should be considered as a rare cause of biliary cirrhosis in patients with situs inversus totalis which is presented with extrahepatic cholestasis.

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完全性倒位与继发性胆汁性肝硬化1例。
完全性倒位是一种与各种内脏异常相关的先天性异常,但没有关于继发性胆汁性肝硬化与这种情况之间关系的数据。我们在此报告一位58岁女性,因肝外胆汁淤积症而入院。排除所有可能导致胆汁性肝硬化的原因后,根据患者的病史、影像学检查、临床和实验室结果以及组织病理学结果诊断继发性胆汁性肝硬化。经牛磺酸去氧胆酸治疗后,所有生化指标,包括总胆红素/直接胆红素、丙氨酸转氨酶、天冬氨酸转氨酶、碱性磷酸酶和γ -谷氨酰转移酶,在治疗第二个月恢复到正常范围。我们认为这是文献中第一个可能表明完全性倒位患者发生继发性胆汁性肝硬化的病例。综上所述,完全性倒位患者表现为肝外胆汁淤积,倒位应被认为是导致胆汁性肝硬化的罕见原因。
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