Case Reports in Transplantation (Jan 2015)

Acute Sickle Hepatic Crisis after Liver Transplantation in a Patient with Hb SC Disease

  • J. H. Gillis,
  • S. K. Satapathy,
  • L. Parsa,
  • P. B. Sylvestre,
  • N. Dbouk

DOI
https://doi.org/10.1155/2015/761740
Journal volume & issue
Vol. 2015

Abstract

Read online

Acute sickle hepatic crisis (ASHC) has been observed in approximately 10% of patients with sickle cell disease. It occurs predominantly in patients with homozygous (Hb SS) sickle cell anemia and to a lesser degree in patients with Hb SC disease, sickle cell trait, and Hb S beta thalassemia. Patients commonly present with jaundice, right upper quadrant pain, nausea, low-grade fever, tender hepatomegaly, and mild to moderate elevations in serum AST, ALT, and bilirubin. We describe the case of a patient with a history of hemoglobin SC disease and cirrhosis caused by hepatitis C presenting approximately 1 year after liver transplantation with an ASHC. The diagnosis was confirmed by liver biopsy. Our patient was treated with RBC exchange transfusions, IV hydration, and analgesia and made a complete recovery. Only a limited number of patients with sickle cell disease have received liver transplants, and, to our knowledge, this is the first case of ASHC after transplantation in a patient with Hb SC disease.