Vaisbuch Edi, Romero Roberto, Kusanovic Juan Pedro, Erez Offer, Mazaki-Tovi Shali, Gotsch Francesca, Kim Chong Jai, Kim Jung-Sun, Yeo Lami, Hassan Sonia S
Perinatology Research Branch, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Department of Health and Human Services, Bethesda, Maryland, USA.
J Ultrasound Med. 2009 Mar;28(3):359-68. doi: 10.7863/jum.2009.28.3.359.
Placental mesenchymal dysplasia (PMD) is an uncommon vascular anomaly of the placenta characterized by mesenchymal stem villous hyperplasia. Its main sonographic feature is a thickened placenta with hypoechoic areas, and an accurate sonographic diagnosis is challenging. The aim of this study was to report 2 cases of PMD and discuss the differential diagnosis of its sonographic features.
Cases of placental masses were studied by 2-dimensional (2D), 3-dimensional (3D), and color Doppler imaging.
In case 1, a thick placenta with multiple hypoechoic areas was noted at 13 weeks' gestation. At 19 weeks, the multicystic area, clearly demarcated from a normal-looking placenta, measured 6.5 x 8.5 cm and enlarged gradually. The patient gave birth to a 625-g female neonate after spontaneous labor at almost 26 weeks' gestation. In case 2, a first sonographic examination at 25 weeks' gestation revealed a thickened placenta with hypoechoic areas and a fetus with a single umbilical artery and a ventricular septal defect. At 27 weeks, the abnormal area of the placenta measured 14.5 x 7.5 cm. At 32 weeks' gestation, a caesarean delivery was performed because of a nonreassuring fetal heart tracing, and a 1415-g female neonate was delivered. Both cases were evaluated by 2D, 3D, and color Doppler imaging, and the pathologic features of both placentas were consistent with PMD.
Placental mesenchymal dysplasia should be considered in the differential diagnosis of every placental mass, especially in cases of multicystic placental lesion with lack of high-velocity signals inside the lesion, and a normal karyotype.
胎盘间质性发育异常(PMD)是一种罕见的胎盘血管异常,其特征为间充质干细胞绒毛增生。其主要超声特征是胎盘增厚并伴有低回声区,准确的超声诊断具有挑战性。本研究的目的是报告2例PMD病例,并讨论其超声特征的鉴别诊断。
采用二维(2D)、三维(3D)和彩色多普勒成像对胎盘肿块病例进行研究。
病例1,孕13周时发现胎盘增厚,有多个低回声区。孕19周时,与外观正常的胎盘界限清晰的多囊区大小为6.5×8.5 cm,并逐渐增大。该患者在孕26周左右自然分娩出一名体重625 g的女婴。病例2,孕25周首次超声检查发现胎盘增厚伴低回声区,胎儿有单脐动脉和室间隔缺损。孕27周时,胎盘异常区域大小为14.5×7.5 cm。孕32周时,因胎儿心率监护结果不令人放心而行剖宫产,娩出一名体重1415 g的女婴。两例均经2D、3D和彩色多普勒成像评估,两个胎盘的病理特征均符合PMD。
在对每一个胎盘肿块进行鉴别诊断时,尤其是对于多囊性胎盘病变且病变内部缺乏高速信号以及核型正常的病例,应考虑胎盘间质性发育异常。