Persistent Cholestasis Following Cholecystectomy: A Case of Dubin-Johnson Syndrome

Journal of Pediatrics

Volumn 157, Issue 1, 2010, Pages 167-

  Renault, Macey ^a   Nowicki, Michael ^a  

^a UNIVERSITY OF MISSISSIPPI SCHOOL OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

BILIRUBIN; COPROPORPHYRIN;

ADOLESCENT; ARTICLE; BILIRUBIN BLOOD LEVEL; BLOOD ANALYSIS; CASE REPORT; CHOLECYSTECTOMY; CHOLESTASIS; DUBIN JOHNSON SYNDROME; FEMALE; HUMAN; HUMAN TISSUE; LIVER BIOPSY; POSTOPERATIVE PERIOD; PRIORITY JOURNAL;

ADOLESCENT; BILIRUBIN; BIOPSY; CHOLECYSTECTOMY; CHOLESTASIS; DIAGNOSIS, DIFFERENTIAL; FEMALE; HUMANS; JAUNDICE, CHRONIC IDIOPATHIC; LIVER;

EID: 77953284609     PISSN: 00223476     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jpeds.2010.01.006     Document Type: Article

References (3)

1. Dubin I., and Johnson F. Chronic idiopathic jaundice with unidentified pigment in liver cells: a new clinicopathologic entity with a report of 12 cases. Medicine 33 (1954) 155-197
2. Paulusma C.C., Kool M., Bosma P.J., Scheffer G.L., ter Borg F., Scheper R.J., et al. A mutation in the human canalicular multispecific organic anion transporter gene causes the Dubin-Johnson syndrome. Hepatology 25 (1997) 1539-1542
3. Koskelo P., Toivonen I., and Adlercreutz H. Urinary coproporphyrin isomer distribution in the Dubin-Johnson syndrome. Clin Chem 13 (1967) 1006-1009