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七例患有先天性心脏异常、肺叶分叶缺陷且内脏心房排列正常的胎儿的尸检及超声心动图检查结果

Autoptic and echocardiographic findings in seven foetuses with congenital heart anomalies, lung lobation defects and normal visceroatrial arrangement.

作者信息

Angiero F, Fesslova V, Rizzuti T, Stefani M

机构信息

Department of Pathology, University of Milan-Bicocca, San Gerardo Hospital, Milan.

出版信息

Pathologica. 2011 Jun;103(3):53-60.

Abstract

OBJECTIVES

Congenital heart defects may be associated with various extracardiac and chromosomal anomalies, and complex cardiac defects may occur in the presence of heterotaxy syndromes, in which both lungs are bilobate, in left isomerism, or both trilobate, in right isomerism. Lung lobation defects are otherwise very rare. Lung lobation is recognisable only at autopsy; however, its definition is fundamental for evaluation of the visceroatrial arrangement, together with other characteristic signs.

METHOD

We report seven cases of congenital heart defects diagnosed prenatally at 14-31 weeks of gestation (wg), 5 females and 2 males, in which autopsy revealed lung lobation defects in the presence of normal visceroatrial arrangement, in association with other extracardiac anomalies or dysmorphism.

RESULTS

Three foetuses had hypoplastic left heart syndrome, one had corrected transposition of great arteries, one had tricuspid atresia, one Ebstein's anomaly and one had ventricular septal defect in trisomy 21. In six cases, pregnancy had been terminated, while the foetus with Ebstein's anomaly died in utero at 32 wg for supraventricular tachycardia. Monolobate, bilobate, trilobate and quadrilobate lungs were found in these foetuses, together with other minor extracardiac anomalies or dysmorphism.

CONCLUSIONS

Autoptic analysis in cases with prenatal diagnosis is needed to confirm echographic findings and reveal other minor anomalies, undetectable by ultrasound imaging that may complete the malformation pattern, which is useful to the couple for genetic counselling.

摘要

目的

先天性心脏缺陷可能与各种心外和染色体异常相关,复杂的心脏缺陷可能发生在脏器异位综合征的情况下,其中在左位异构时两肺均为两叶,或在右位异构时两肺均为三叶。否则,肺叶划分缺陷非常罕见。肺叶划分仅在尸检时可识别;然而,其定义对于评估内脏心房排列以及其他特征性体征至关重要。

方法

我们报告了7例在妊娠14 - 31周产前诊断为先天性心脏缺陷的病例,5例女性和2例男性,尸检显示在正常内脏心房排列的情况下存在肺叶划分缺陷,并伴有其他心外异常或畸形。

结果

3例胎儿患有左心发育不全综合征,1例患有矫正型大动脉转位,1例患有三尖瓣闭锁,1例患有埃布斯坦畸形,1例患有21三体综合征合并室间隔缺损。6例妊娠已终止,而患有埃布斯坦畸形的胎儿在妊娠32周时因室上性心动过速死于宫内。在这些胎儿中发现了单叶、两叶、三叶和四叶肺,以及其他轻微的心外异常或畸形。

结论

对于产前诊断的病例,需要进行尸检分析以确认超声检查结果,并揭示超声成像无法检测到的其他轻微异常,这些异常可能完善畸形模式,这对夫妇进行遗传咨询很有用。

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