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자료유형
학술저널
저자정보
진민지 (계명대학교) 김윤겸 (계명대학교) 최은미 (계명대학교) 심예지 (계명대학교) 김형식 (계명대학교) 서진경 (가천대학교 길병원) 김지윤 (경북대학교) 이건수 (경북대학교) 박선영 (영남대학교) 이재민 (영남대학교) 하정옥 (대구파티마병원)
저널정보
대한혈액학회 Blood Research Blood Research Vol.53 No.2
발행연도
2018.1
수록면
110 - 116 (7page)

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Background Cytomegalovirus (CMV) causes severe diseases in premature infants and immunocompromised hosts, and antiviral therapy is often required for disease control. However, the clinical manifestations and treatment courses for CMV-associated thrombocytopenia in immunocompetent children are unclear. Methods Medical records of the children who suffered from thrombocytopenia, and showed pos-itive CMV polymerase chain reaction and CMV-like symptoms were retrospectively analyzed at three university hospitals in Daegu from January 2000 to March 2017. Patients suffering from leukemia, immunodeficiency, and other infections were excluded. Results Among 1,065 children with thrombocytopenia, 29 (2.7%) displayed CMV-associated thrombocytopenia. The median age at diagnosis was 15 months and the median platelet count was 26,000/L. They were classified into the CMV-induced thrombocytopenia (23/29) and CMV-related secondary immune thrombocytopenia (ITP, 6/29) groups. Fourteen subjects had hepatic dysfunction, four had Evans syndrome, two had pneumonitis, and one had gastritis. IVIG was used for 21 patients, and six patients among them showed recurrence, for whom IVIG or antiviral therapy was used. All, except one, re-current or chronic cases belonged to the CMV-induced thrombocytopenia group. Antiviral therapy was used more frequently for the CMV-induced thrombocytopenia group (8/23, 34.8%) than for the CMV-related secondary ITP group (0/6); however, the results were not statistically significant (P=0.148). Conclusion CMV is a rare but unique etiology of thrombocytopenia, and observed even in healthy children after the neonatal period. About one-third patients need antiviral therapy for dis-ease control. Further, CMV-induced thrombocytopenia is more complex than CMV-related secondary ITP.

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