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이민재 ( Min Jae Lee ),장윤환 ( Yoon Hwan Chang ),강승화 ( Seung Hwa Kang ),문세권 ( Se Kwon Mun ),김혜진 ( Hey Jin Kim ),한철주 ( Chul Ju Han ),김진 ( Jin Kim ),강혜진 ( Hye Jin Kang ) 대한소화기학회 2013 대한소화기학회지 Vol.61 No.3
We recently encountered a case of hereditary spherocytosis coexisting with Gilbert`s syndrome. Patient was initially diagnosed with Gilbert`s syndrome and observed, but other findings suggestive of concurrent hemolysis, such as splenomegaly and gallstones were noted during the follow-up period. Therefore, further evaluations, including a peripheral blood smear, osmotic fragility test, autohemolysis test, and red blood cell membrane protein test were performed, and coexisting hereditary spherocytosis was diagnosed. Genotyping of the conjugation enzyme uridine diphosphate-glucuronosyltransferase was used to confirm Gilbert`s syndrome. Because of the high prevalence rates and similar symptoms of these 2 diseases, hereditary spherocytosis can be masked in patients with Gilbert`s syndrome. In review of a case and other article, the possibility of the coexistence of these 2 diseases should be considered, especially in patients with unconjugated hyperbilirubinemia who also have splenomegaly and gallstones. (Korean J Gastroenterol 2013;61:166-169)