Matsuda T, Yonaha H, Azuma E, Sakurai M, Imai S
Department of Pediatrics, Yonaha Hospital, Mie, Japan.
Am J Hematol. 1990 Nov;35(3):199-202. doi: 10.1002/ajh.2830350311.
We report a Japanese newborn who developed alloimmune thrombocytopenia by the antibodies to the newly discovered platelet antigen Yuk(a). The infant recovered uneventfully in 10 days without specific treatment. Antiplatelet alloantibodies in the patient were IgG class detected by mixed passive hemagglutination (MPHA). Family study showed that Yuk(a) antigen was inherited as an autosomal dominant trait. Cases with Yuk(a)-associated alloimmune thrombocytopenia are reviewed.
我们报告了一名日本新生儿,其因针对新发现的血小板抗原Yuk(a)的抗体而发生同种免疫性血小板减少症。该婴儿未经特殊治疗,于10天内顺利康复。通过混合被动血凝试验(MPHA)检测到患者体内的抗血小板同种抗体为IgG类。家族研究表明,Yuk(a)抗原以常染色体显性性状遗传。本文对与Yuk(a)相关的同种免疫性血小板减少症病例进行了综述。