Acardiac acephalus: a case report and implications on expectant management.

Changgeng yi xue za zhi Pub Date : 1999-06-01
K S Law, S D Chang, F P Chen, Y K Soong
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Abstract

Acardiac acephalus is a rare occurrence resulting from extensive anastomoses between the vessels of the monochorionic twins which invariably leads to death of the "perfused" twin and an estimated 50% perinatal mortality rate in the "pump" twin, due mainly to premature delivery or congestive heart failure. Once diagnosis has been documented, blocking the vascular flows between the twins has been the principle goal of treatment with the assumption that a more favorable chance of survival in the pump twin can be achieved. However, hasty surgical intervention without a well-designed preoperative evaluation may result in unfavorable outcomes. A 21-year-old nullipara was found to carry an acardiac parabiotic twin in a monochorionic twin pregnancy at 28 weeks of gestation and was referred to us from a local clinic. Expectant management based on the close monitoring of the well-being of the healthy co-twin is presented in this article along with review of published works on the management of this rare condition.

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心源性脑瘫:1例报告及对预期治疗的启示。
心源性脑瘫是一种罕见的情况,由于单绒毛膜双胞胎的血管之间广泛吻合,这种情况总是导致“灌注型”双胞胎死亡,而“泵型”双胞胎的围产期死亡率估计为50%,主要原因是早产或充血性心力衰竭。一旦确诊,阻断双胞胎之间的血管流动一直是治疗的主要目标,假设泵双胞胎可以实现更有利的生存机会。然而,仓促的手术干预,没有良好设计的术前评估可能导致不利的结果。一位21岁的无孕妇女在妊娠28周时被发现携带一个心脏异位双胞胎,并从当地一家诊所转介到我们这里。基于对健康双胞胎健康状况的密切监测的期望管理在本文中提出,并回顾了有关这种罕见疾病管理的已发表作品。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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