Korean J Pediatr.  2004 Aug;47(8):892-895.

Two Cases of Rotor Syndrome in Siblings

Affiliations
  • 1Department of Pediatrics, College of Medicine, Kyung Hee University, Seoul, Korea. tcha0319@pednet.co.kr
  • 2Department of Nuclear Medicine, College of Medicine, Kyung Hee University, Seoul, Korea.

Abstract

Rotor syndrome is a rare benign familial disorder characterized by chronic, fluctuating, nonhemolytic and predominantly direct bilirubinemia with normal liver tissue. We have recently experienced two cases of Rotor syndrome in a brother and sister. They revealed icteric sclerae with mild hepatomegaly in physical examination. Laboratory findings showed increased serum bilirubin with direct bilirubin predominance. The urinary excretion of total coproporphyrin was slightly elevated. The 99mTc-DISIDA scan showed a markedly decreased hepatic uptake and poor visualization of gallbladder and biliary tree which could be compatible to the Rotor syndrome. We report two cases with a review of the literature.

Keyword

Rotor syndrome; Hyperbilirubinemia

MeSH Terms

Biliary Tract
Bilirubin
Gallbladder
Hepatomegaly
Humans
Hyperbilirubinemia
Hyperbilirubinemia, Hereditary*
Liver
Physical Examination
Sclera
Siblings*
Technetium Tc 99m Disofenin
Bilirubin
Technetium Tc 99m Disofenin
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