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心脏未发育的双胎之一,外置肠管附着于胎盘:脐膨出的罕见表现。

Acardiac twin with externalized intestine adherent to placenta: unusual manifestation of omphalocele.

作者信息

Emery Shawn Clark, Vaux Keith K, Pretorius Dolores, Masliah Eliezer, Benirschke Kurt

机构信息

Department of Pathology, Autopsy Service, University of California San Diego Medical Center, 200 West Arbor Drive, San Diego, CA 92103-8321, USA.

出版信息

Pediatr Dev Pathol. 2004 Jan-Feb;7(1):81-5. doi: 10.1007/s10024-003-5052-8.

Abstract

TRAP (twin reversed arterial perfusion) syndrome produces an acardiac twin (acardiac monster, acardius, acardiacus, chorioangiopagus parasiticus, etc.). Acardiacs result from monozygotic multiple births in which three anatomic anomalies occur: (1) a fetus' cardiac development is disturbed; (2) artery-artery anastomosis carries blood from a normal ("pump") twin to the acardiac; (3) vein-vein anastomosis carries blood from the acardiac back to the normal twin. Whether reversal of blood flow in the acardiac results from or causes cardiac dysmorphogenesis has not been resolved. Acardiac twins demonstrate a complex constellation of malformations usually thought to result from reversed blood flow; omphalocele is particularly common. We report monochorionic monoamnionic male twins in which an acardiac twin demonstrated externalized intestines adherent to the placenta. The twins were delivered from a 30-year-old primigravida mother by cesarean section without maternal complications at 33 w. The mother has no significant past medical history. The macerated acardius had a 4-cm long attenuated umbilical cord with indeterminate number of vessels. Structures rostral to the thorax were absent save for one poorly developed hand and arm. The abdomen contained loose mesenchyme and no organs. The entire intestine (21 cm) along with two testes was located in a sac on the surface of the placenta. No histopathologic anomalies of formed structures were identified aside from spatial relationships and incomplete development. The normal twin required no intensive care and is doing well. To our knowledge, this is the first report of externalized intestine, which may represent an unusual consequence of omphalocele.

摘要

双胎反向动脉灌注(TRAP)综合征会产生无心双胎(无心畸胎、无心儿、寄生胎等)。无心双胎源于单卵多胎妊娠,其中会出现三种解剖学异常:(1)一个胎儿的心脏发育受到干扰;(2)动脉-动脉吻合将血液从正常(“泵血”)双胎输送到无心双胎;(3)静脉-静脉吻合将血液从无心双胎回流到正常双胎。无心双胎中血流逆转是由心脏发育异常引起还是导致心脏发育异常尚未明确。无心双胎表现出一系列复杂的畸形,通常认为是由血流逆转导致的;脐膨出尤为常见。我们报告了一对单绒毛膜单羊膜囊男性双胎,其中一个无心双胎的外露肠管附着于胎盘。这对双胎由一位30岁的初产妇母亲在孕33周时剖宫产分娩,母亲无并发症。母亲既往无重大病史。浸软的无心儿有一条4厘米长、血管数量不定的变细脐带。除了一只发育不良的手和手臂外胸廓上方无结构。腹部有疏松间充质,无器官。整个肠管(21厘米)连同两个睾丸位于胎盘表面的一个囊中。除空间关系和发育不全外,未发现成形结构的组织病理学异常。正常双胎无需重症监护,情况良好。据我们所知,这是外露肠管的首例报告,这可能代表脐膨出的一种罕见后果。

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