Miyake T, Yokoyama T, Shinohara T, Seto S, Oiki M
Department of Cardiovascular Surgery, Kinki University School of Medicine, Osaka-Sayama, Japan.
Acta Paediatr Jpn. 1995 Aug;37(4):521-5. doi: 10.1111/j.1442-200x.1995.tb03368.x.
We report on an 8 month old infant with Kawasaki disease associated with giant coronary aneurysms and transient thrombocytopenia. The patient's platelet count decreased to 24,000/mm3 on the 31st day of illness and fibrin degradation product was 5 micrograms/mL. Platelet count increased to the normal level (357,000/mm3) on the 35th day of illness. On the 27th day of illness, dilatation of the distal abdominal aorta adjacent to the bifurcation of the iliac arteries was observed by B-mode and color Doppler ultrasonography. It gradually returned to a normal size by the 45th day of illness. Aspirin administered from the 3rd to the 26th day of illness was replaced with flubioprophen because of liver dysfunction. Although we can not eliminate aspirin allergy as the cause of the transient thrombocytopenia, we think that the thrombocytopenia may have been related to the regression of the abdominal aorta.
我们报告了一名8个月大的患有川崎病的婴儿,该患儿伴有巨大冠状动脉瘤和短暂性血小板减少症。患儿在发病第31天血小板计数降至24,000/mm³,纤维蛋白降解产物为5微克/毫升。发病第35天血小板计数升至正常水平(357,000/mm³)。发病第27天,通过B超和彩色多普勒超声检查发现髂动脉分叉处附近的腹主动脉远端扩张。到发病第45天,其逐渐恢复至正常大小。由于肝功能异常,发病第3天至第26天使用的阿司匹林被氟比洛芬替代。虽然我们不能排除阿司匹林过敏是短暂性血小板减少症的病因,但我们认为血小板减少症可能与腹主动脉的恢复有关。