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并腿畸形合并食管闭锁：一种罕见的关联。

Sirenomelia with oesophageal atresia: a rare association.

作者信息

Sathe Pragati Aditya, Ghodke Ratnaprabha Kundlikrao, Kandalkar Bhuvaneshwari Mahendra

机构信息

Associate Professor, Department of Pathology, Seth G.S. Medical College & KEM Hospital , Mumbai, India .

Professor, Department of Pathology, Seth G.S. Medical College & KEM Hospital , Mumbai, India .

出版信息

J Clin Diagn Res. 2014 Feb;8(2):163-4. doi: 10.7860/JCDR/2014/8045.4044. Epub 2014 Feb 3.

DOI:10.7860/JCDR/2014/8045.4044
PMID:24701519
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3972546/
Abstract

We are reporting a rare case of sirenomelia with oesophageal atresia. Sirenomelia is a lethal sporadic defect of which lower gastrointestinal tract anomalies are characteristic findings. Respiratory and upper gastrointestinal tract malformations like oesophageal atresia occur in about 20-35% of cases. Though its occurrence has been described, it has been reported only rarely. This report aims at describing this uncommon association along with its histological features.

摘要

我们报告了一例罕见的并伴有食管闭锁的下肢联体畸形病例。下肢联体畸形是一种致命的散发性缺陷，其特征性表现为下消化道异常。呼吸和上消化道畸形，如食管闭锁，约20%-35%的病例会出现。虽然其发生情况已有描述，但报道仍很罕见。本报告旨在描述这种罕见的关联及其组织学特征。

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本文引用的文献

1
The sirenomelia sequence: a case history.人鱼序列征：一例病史
Clin Med Insights Case Rep. 2010;3:41-9. doi: 10.4137/ccrep.s5347. Epub 2010 Aug 13.
2
A surviving infant with sirenomelia (Mermaid syndrome) associated with absent bladder.一名患有并腿畸形（美人鱼综合征）且膀胱缺如的存活婴儿。
J Pediatr Surg. 2003 Aug;38(8):1266-8. doi: 10.1016/s0022-3468(03)00286-0.
3
Caudal regression syndrome versus sirenomelia: a case report.尾部退化综合征与美人鱼综合征：一例报告
J Perinatol. 2002 Mar;22(2):168-70. doi: 10.1038/sj.jp.7210598.
4
Sirenomelia with esophageal atresia.并腿畸形合并食管闭锁
Adv Clin Path. 2000 Oct;4(4):165-8.