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肛门直肠畸形的产前影像学——瑞士一家三级中心的 10 年经验。

Prenatal imaging of anorectal malformations - 10-year experience at a tertiary center in Switzerland.

机构信息

Department of Diagnostic and Interventional Radiology, CHUV - Centre Hospitalier Universitaire Vaudois, Rue du Bugnon 21, 1011, Lausanne, Switzerland.

Department of Gynecology and Obstetrics, CHUV - Centre Hospitalier Universitaire Vaudois, Lausanne, Switzerland.

出版信息

Pediatr Radiol. 2020 Jan;50(1):57-67. doi: 10.1007/s00247-019-04513-2. Epub 2019 Sep 3.

Abstract

BACKGROUND

Anorectal malformation is a spectrum of congenital defects of the distal bowel, mostly diagnosed at birth.

OBJECTIVE

To describe the prenatal imaging findings of anorectal malformations, explore the causes of the low rates of prenatal diagnosis, compare the accuracy of prenatal ultrasound (US) and magnetic resonnance imaging [MRI] and evaluate the relevance of information obtained at MRI.

MATERIALS AND METHODS

Children treated for anorectal malformation at our hospital and with available prenatal studies were retrospectively identified and included in the study. We reviewed prenatal imaging exams, listed findings suggestive of the diagnosis, and compared results with the final classification.

RESULTS

Fourteen fetuses and neonates - eight with intermediate-high type anorectal malformation and six with cloacae - fulfilled the inclusion criteria. All had associated congenital anomalies. Prenatal exams included 13 US and 8 MRI exams, with 7 children having both exams. Suggestive findings for anorectal malformation were detected in 50% of the cases prenatally and in 85% upon review. They were prospectively detected in 31% and 50% of the cases at US and MRI and retrospectively in 62% and 100% at US and MRI, respectively. MRI was superior to US because it improved the diagnosis, especially in cloacae, and provided relevant additional information that changed management in two cases.

CONCLUSION

The most important signs suggesting anorectal malformation are an absent target sign and anomalous distal bowel wall and rectal fluid. Complementary prenatal MRI improves the diagnosis of anorectal malformation.

摘要

背景

肛门直肠畸形是一种远端肠先天性缺陷的谱系,大多数在出生时诊断。

目的

描述肛门直肠畸形的产前影像学表现,探讨产前诊断率低的原因,比较产前超声(US)和磁共振成像(MRI)的准确性,并评估 MRI 获得的信息的相关性。

材料和方法

回顾性地确定了在我院接受肛门直肠畸形治疗且有可用产前研究的儿童,并将其纳入研究。我们复习了产前影像学检查,列出了提示诊断的发现,并将结果与最终分类进行了比较。

结果

14 名胎儿和新生儿(8 名具有中高位肛门直肠畸形,6 名具有直肠会阴瘘)符合纳入标准。所有患儿均伴有先天性畸形。产前检查包括 13 次 US 和 8 次 MRI 检查,其中 7 名患儿同时进行了这两种检查。50%的病例在产前检查中发现了肛门直肠畸形的提示性发现,85%在复查时发现。US 前瞻性检测出 31%,MRI 前瞻性检测出 50%,US 回顾性检测出 62%,MRI 回顾性检测出 100%。MRI 优于 US,因为它提高了诊断率,尤其是在直肠会阴瘘中,并提供了相关的额外信息,这在 2 例中改变了治疗方案。

结论

提示肛门直肠畸形最重要的征象是靶征缺失和远端肠壁及直肠内液异常。补充性产前 MRI 可提高肛门直肠畸形的诊断率。

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