Department of Pediatric Newborn Medicine, Brigham and Women's Hospital, Boston, Massachusetts.
Medical Genetics Unit, MassGeneral Hospital for Children, Boston, Massachusetts.
Birth Defects Res. 2018 Jan;110(2):98-107. doi: 10.1002/bdr2.1160.
Several malformations have been attributed to the process of vascular disruption. The central hypothesis for this etiology is that blood flow to a structure has been altered after that structure had formed normally. The decreased blood flow leads to hypoxia, endothelial cell damage, hemorrhage, tissue loss, and repair. After recovery, some structures are normal and others show either tissue loss or structural abnormalities, such as syndactyly and constriction rings.
The phenotypic features of the 7,020 infants with one or more malformations, who were born to women who had always planned to deliver at Brigham and Women's Hospital (BWH) between, 1972 and 2012, that is, maternal nontransfers, were reviewed. The phenotypes associated with vascular disruption, such as the amniotic band syndrome and terminal transverse limb defects (TTLD), were identified.
One hundred and five fetuses and infants had malformations attributed to the process of vascular disruption. Some specific causes of the amniotic band limb deformity were identified. TTLD with associated small digit-like nubbins occurred at three levels: proximal forearm, wrist, and metacarpal-phalangeal joint. Other causes included severe hemoglobinopathies and exposures to misoprostol and to prenatal procedures.
Malformations attributed to the process of vascular disruption were a distinctive entity, among the recognized etiologies. The timing of the causative event in the first trimester was established for infants with exposures to either the prostaglandin misoprostol or the prenatal diagnosis procedure chorionic villus sampling. One challenge is to identify the developmental steps in vascular disruption when no causative exposure can be identified.
多种畸形归因于血管破坏过程。该病因的中心假说认为,结构正常形成后,其血流发生改变。血流量减少导致缺氧、内皮细胞损伤、出血、组织丢失和修复。恢复后,一些结构正常,而另一些则表现为组织丢失或结构异常,如并指和缩窄环。
回顾了 1972 年至 2012 年期间,一直在布里格姆妇女医院(BWH)分娩且从未打算转院的妇女所生的 7020 名有一个或多个畸形的婴儿的表型特征。鉴定了与血管破坏相关的表型特征,如羊膜带综合征和末端横断肢体缺陷(TTLD)。
105 例胎儿和婴儿的畸形归因于血管破坏过程。确定了羊膜带肢体畸形的一些特定原因。与小指状小结相连的 TTLD 发生在三个水平:前臂近端、手腕和掌指关节。其他原因包括严重的血红蛋白病以及米索前列醇和产前程序的暴露。
血管破坏过程引起的畸形是一种独特的实体,属于已识别的病因之一。在第一孕期确定了因暴露于前列腺素米索前列醇或产前诊断程序绒毛膜绒毛取样而导致的婴儿发病事件的时间。当无法确定致病暴露时,确定血管破坏中的发育步骤是一个挑战。