A Case of Rotor Syndrome

Rotor 증후군 1예

Rotor syndrome is a rare disease of hereditary hyperbilirubinemia transmitted with autosomal recessive trait. In general, Rotor syndrome shows direct hyperbilirubinemia and there has been several reports since Sons's report in 1966, in Korea. A 34-year-old female with admitted with the chief complaint of intermittent icteric sclera for 24 years. There was no family history of jaundice. Rotor syndrome was diagnosed by oral cholecystogram, BSP retention test, $^{99m}Tc$-DISIDA scan, liver biopsy and electromiuoscopy study of liver biopsy specimen. We report this case with brief review of the literature.

저자들은 최근 24년간의 간헐적인 만성 황달을 주소로 내원한 34세 여자 환자에서 임상소견, 간기능 검사, 담낭소견, BSP 저류 검사, $^{99m}Tc$-DISIDA스캔 및 간생검법을 시행하여 Rotor증후군으로 확인된 1예를 경험하였기에 문헌고찰과 함께 보고하는 바이다.