Bunjevacki G, Stojimirović E, Jevdević M
Bilt Hematol Transfuz. 1981;9(1-3):105-12.
The paper presents a patient J.S., aged 2 1/2 years, with thrombocytopenia, presence of giant thrombocytes and basophile inclusions in the granulocytes. The same lesions were found in the child's father, followed by increased tendency to bleeding also confirmed in other four family members. Familiar character of the disease and morphologic anomaly of thrombocytes and leucocytes were the basis in passing the diagnosis of May-Hegglin anomaly. The specific features of the case are the child's age and the appearance of hemorrhagic syndrome in infancy.
该论文介绍了一名2岁半的患者J.S.，其患有血小板减少症，存在巨大血小板以及粒细胞中的嗜碱性包涵体。在孩子的父亲身上也发现了同样的病变，另外四名家庭成员也证实有出血倾向增加的情况。疾病的家族特征以及血小板和白细胞的形态异常是做出May-Hegglin异常诊断的依据。该病例的特殊之处在于患儿的年龄以及婴儿期出现的出血综合征。
