Dubin–Johnson Syndrome: An Eight-Year Retrospective Clinicopathological Review from a North Indian Tertiary Center

Abstract

Background and aims

Dubin–Johnson syndrome (DJS) is an uncommon disease with a characteristic clinical and biochemical profile, rarely requiring diagnostic liver biopsy. Indian data on the clinicopathological spectrum of DJS are scant. The study is aimed at the analysis of the clinical context for liver biopsy, histological spectrum, utility of special stains, and multidrug resistance-associated protein 2 (MRP2) immunohistochemistry in DJS.

Materials and methods

The clinical presentation, hematological, and biochemical parameters of all biopsy-proven cases of DJS in the last eight years (N = 15, 16 biopsies) were gleaned from the archives. All biopsies were stained with routine hematoxylin and eosin stain, various special stains, MRP2, bile salt export pump, and CK7 immunostains.

Results

The median age of presentation of DJS was 26.5 years (interquartile range [IQR]: 19–60.5 years). Nine of 15 patients (60%) had an additional liver disorder (chronic viral hepatitis, non-cirrhotic portal fibrosis, cirrhosis, etc). One-third of the cases were diagnosed on histology alone (clinically unsuspected). All cases showed conjugated hyperbilirubinemia (median total bilirubin: 5.1 mg/dL, IQR: 4.3–8.1 mg/dL) with normal liver enzymes and hemogram. All biopsies showed centrilobular-dominant deposition of pseudomelanin pigment in the hepatocytes and Kupffer cells. MRP2 immunostain showed complete loss of (85.7%)/partial canalicular (14.3%) expression.

Conclusion

The clinical features of DJS are often obscured/altered by a coexistent liver disease necessitating liver biopsy. Histological documentation of the pigment by a panel of special stains is required for diagnosis. Loss of canalicular MRP2 expression complements special stains when pigment is scant and should be considered in diagnostically challenging biopsies.