Boulot P, Sunol J, Sarda P, Deschamps F, Hedon B, Laffargue F, Viala J L
Centre de Foetologie, Montpellier.
Presse Med. 1989 Dec 9;18(41):2004-6.
Severe foetal thrombocytopenia (24,000 platelets per cubic mm) was diagnosed in a 37-week pregnant woman. The primigravida, primipara mother had been affected with idiopathic thrombocytopenic purpura at the age of 6 years, in remission since the age of 8 years (after splenectomy). The prenatal diagnosis was made by foetal blood sampling performed when the mother's platelet count was normal. The expected haemorrhagic complications of vaginal delivery were avoided by a caesarean section.
一名37周孕妇被诊断为严重胎儿血小板减少症(每立方毫米24,000个血小板)。这位初产妇、初孕母亲在6岁时曾患特发性血小板减少性紫癜,8岁(脾切除术后)病情缓解。产前诊断是在母亲血小板计数正常时通过胎儿采血进行的。剖宫产避免了阴道分娩预期的出血并发症。