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一名患有遗传性球形红细胞增多症、吉尔伯特综合征和梗阻性黄疸的患者出现极重度高胆红素血症。

Extreme hyperbilirubinemia in a patient with hereditary spherocytosis, Gilbert's syndrome, and obstructive jaundice.

作者信息

Katz M E, Weinstein I M

出版信息

Am J Med Sci. 1978 May-Jun;275(3):373-9. doi: 10.1097/00000441-197805000-00016.

Abstract

Hyperbilirubinemia may be of several etiologies in the individual patient. An 18-year-old man presented with extreme hyperbilirubinemia (direct bilirubin 23.0 mg/dl, total bilirubin 60.0 mg/dl), hepatosplenomegaly, and anemia. Hematologic studies prelaparotomy documented the presence of hereditary spherocytosis. Intraoperative liver biopsy revealed moderately reduced levels of glucuronyl transferase activity (Gilbert's syndrome). Common bile duct obstruction secondary to choledocholithiasis was found, and a cholecystectomy and splenectomy were performed. This case stresses the potential confusion among several diseases which may present with hyperbilirubinemia.

摘要

个体患者的高胆红素血症可能有多种病因。一名18岁男性出现极度高胆红素血症(直接胆红素23.0mg/dl,总胆红素60.0mg/dl)、肝脾肿大和贫血。剖腹手术前的血液学检查证实存在遗传性球形红细胞增多症。术中肝脏活检显示葡萄糖醛酸转移酶活性水平中度降低(吉尔伯特综合征)。发现胆总管结石继发胆总管梗阻,并进行了胆囊切除术和脾切除术。该病例强调了几种可能表现为高胆红素血症的疾病之间可能存在的混淆。

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