Dubin-Johnson syndrome

Dubin-Johnson syndrome (DJS) is a benign, inherited liver disorder characterized clinically by chronic, predominantly conjugated, hyperbilirubinemia and histopathologically by black-brown pigment deposition in parenchymal liver cells.

Cholecystitis

The presence of inflammatory changes in the gallbladder.


Total: 2

                       


(per page)
PMID (PMCID)
10979180
 MALE Middle Aged
Incipient perisinusoidal fibrosis in an adult patient with Dubin-Johnson syndrome.
Kuvandzhiev GK, Zaprianov ZN, Dikov DI.
Folia Med (Plovdiv). 2000;42(1):62-5.
The present paper describes a rare case of incipient perisinusoidal fibrosis of perihepatocellular type occurring in the Dubin-Johnson syndrome in a 63-year-old patient operated on six months previously for chronic calculous cholecystitis.
6635916
 MALE Adult
Cholelithiasis in Dubin-Johnson syndrome.
Skornick YG, Klausner JM, Lelcuk S, Merhav A, Ratan J, Rozin RR.
Surg Gynecol Obstet. 1983;157(5):447-9.
We present one additional patient, a 30 year old man with Dubin-Johnson syndrome in whom pancreatitis and cholecystitis, secondary to cholesterol gallstones, developed.