Fineschi Vittorio, Riezzo Irene, Cantatore Santina, Pomara Cristoforo, Turillazzi Emanuela, Neri Margherita
Department of Forensic Pathology, University of Foggia, Ospedale Colonnello D'Avanzo, Via degli Aviatori 1, 71100, Foggia, Italy.
Virchows Arch. 2009 Mar;454(3):283-90. doi: 10.1007/s00428-009-0730-1. Epub 2009 Jan 27.
To date, the most recent specific diagnostic investigations for amniotic fluid embolism have been unable to conclusively identify any mechanism of disease other than a physical block to the circulation. We selected eight fatal cases in previously healthy women with uneventful singleton term pregnancies who presented to tertiary care centers in Italy for delivery. Pathologic features were assessed immunohistochemically using anti-fibrinogen, anti-tryptase, anti-C(3a), and anti-cytokeratin antibodies. AE1/AE3 cytokeratin stains proved positive, and tryptase-positive material was documented outside pulmonary mast cells. In all studied cases, expression of complement C(3a) was twofold lower than in the control group, suggesting a possible complement activation in AFE, initiated by fetal antigen leaking into the maternal circulation.
迄今为止,除了循环系统的物理阻塞外,针对羊水栓塞的最新特异性诊断研究未能确凿地确定任何疾病机制。我们选择了8例在意大利三级医疗中心分娩的单胎足月妊娠、既往健康的女性死亡病例。使用抗纤维蛋白原、抗胰蛋白酶、抗C(3a)和抗细胞角蛋白抗体通过免疫组织化学评估病理特征。AE1/AE3细胞角蛋白染色呈阳性,且在肺肥大细胞外记录到了胰蛋白酶阳性物质。在所有研究病例中,补体C(3a)的表达比对照组低两倍,提示羊水栓塞可能存在补体激活,由胎儿抗原漏入母体循环引发。