1.
J Clin Diagn Res
; 9(2): OD03-4, 2015 Feb.
Artigo
em Inglês
| MEDLINE
| ID: mdl-25859482
RESUMO
Hepatobiliary complications of sickle cell disease are relatively rare but well recognised in literature. Clinical syndromes range from mild intrahepatic cholestasis and gallstones to life threatening sequestration crisis. Most patients, homozygous for sickle cell anaemia, present before adolescence. We report a case of an adult man with no prior symptoms who presented for the first time with decompensated cirrhosis, which was found to be due to underlying previously unrecognised sickle cell anaemia.
2.
BMJ Case Rep
; 20142014 Jun 02.
Artigo
em Inglês
| MEDLINE
| ID: mdl-24891489