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单绒毛膜双羊膜囊双胎妊娠中的体蒂异常——病例报告及文献复习

Body stalk anomaly in a monochorionic-diamniotic twin pregnancy - case report and review of the literature.

作者信息

Bohîlţea Roxana Elena, Tufan Cicerone Florentin, Cîrstoiu Monica Mihaela, Dumitru Adrian Vasile, Georgescu Tiberiu Augustin, Sajin Maria, Bodean Oana Maria, Munteanu Octavian, Brătilă Elvira, Ofiţeru Anca Maria, Berceanu Costin

机构信息

Department of Anatomy, "Carol Davila" University of Medicine and Pharmacy, Bucharest, Romania;

出版信息

Rom J Morphol Embryol. 2017;58(4):1453-1460.

Abstract

Body stalk anomaly (BSA) is a rare abdominal defect, generally considered to be lethal. Reported prevalence ranges from 0.4 to 3.2 per 100 000 live births. An early prenatal diagnosis offers the possibility of parental counseling and the termination of pregnancy. Also called limb-body wall complex, the anomaly is characterized by finding the intrathoracic and abdominal organs outside the cavity comprised by amnio-peritoneal membrane attached directly to the placenta and the umbilical cord short or absent. We report a case of BSA in a monochorionic-diamniotic twin pregnancy, diagnosed antenatal by the massive midline thoraco-abdominal wall defect, severe scoliosis and absent umbilical cord, presented at fetal ultrasound first trimester examination; portions of the heart, kidney and lung were contained into the placenta. The second fetus was echographically normal. At 18 weeks of gestation, a recommended amniocentesis exam was performed, an abnormal karyotype being excluded through this method. At 33 weeks of gestation, the patient presented with spontaneous preterm rupture of membranes. Delivery occurred by emergency Caesarean section for acute fetal distress; extracted first live fetus was admitted in the neonatal intensive care; the second live fetus with a severe thoraco-abdominal wall defect, fragments of organs included into the placental mass and severe reduction defect of the inferior right limb, deceased at 30 minutes from delivery. The fetus together with the placenta has been sent for histopathological exam. Clinical examination confirmed the diagnosis suspected by ultrasound examination. There are only a few reports in the literature about BSA in multiple gestations, and fewer about twin pregnancies in which only one fetus was affected by this condition.

摘要

体蒂异常(BSA)是一种罕见的腹部缺陷,通常被认为是致命的。据报道,其患病率为每10万例活产中有0.4至3.2例。早期产前诊断为父母咨询和终止妊娠提供了可能性。这种异常也被称为肢体-体壁复合体,其特征是胸腔和腹腔器官位于由直接附着于胎盘的羊膜-腹膜构成的腔外,脐带短或缺失。我们报告一例单绒毛膜双羊膜囊双胎妊娠中的体蒂异常病例,在孕早期胎儿超声检查时,通过巨大的中线胸腹壁缺损、严重脊柱侧弯和脐带缺失进行产前诊断;心脏、肾脏和肺的部分组织包含在胎盘中。第二个胎儿超声检查正常。妊娠18周时,进行了推荐的羊水穿刺检查,通过该方法排除了异常核型。妊娠33周时,患者出现胎膜早破。因急性胎儿窘迫行急诊剖宫产分娩;取出的第一个活产胎儿被送入新生儿重症监护室;第二个活产胎儿有严重的胸腹壁缺损、器官碎片包含在胎盘团块中以及右下肢严重发育不全,出生后30分钟死亡。胎儿连同胎盘已送去做组织病理学检查。临床检查证实了超声检查怀疑的诊断。文献中关于多胎妊娠中的体蒂异常报道较少,而关于只有一个胎儿受此疾病影响的双胎妊娠报道更少。

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