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肺囊性腺瘤样畸形:产前诊断、预后因素及胎儿结局

Cystic adenomatoid malformation of the lung: prenatal diagnosis, prognostic factors and fetal outcome.

作者信息

Golaszewski T, Bettelheim D, Eppel W, Deutinger J, Bernaschek G

机构信息

Department of Prenatal Diagnosis and Therapy, University of Vienna, Austria.

出版信息

Gynecol Obstet Invest. 1998;46(4):241-6. doi: 10.1159/000010042.

DOI:10.1159/000010042
PMID:9813442
Abstract

AIM

To evaluate 14 cases of cystic adenomatoid malformation (CAM) of the lung with regard to antenatal management and fetal outcome.

RESULTS

Intrauterine shunts were placed in 3 fetuses to avoid pulmonary hypoplasia. Prenatal sonography showed that the lesions had a tendency to resolve in 4 cases. Of the 9 infants who survived, 5 were treated surgically (lobectomy).

CONCLUSIONS

The antenatal evolution of these lesions is highly variable; the lesions may even resolve spontaneously, therefore the diagnosis of CAM types II and III should be followed by a period of observation. Intrauterine drainage is recommended in cases of CAM type I if unfavorable prognostic factors are encountered.

摘要

目的

评估14例肺囊性腺瘤样畸形(CAM)的产前管理及胎儿结局。

结果

3例胎儿接受了宫内分流术以避免肺发育不全。产前超声检查显示4例病变有自行消退的趋势。9例存活婴儿中,5例接受了手术治疗(肺叶切除术)。

结论

这些病变的产前演变差异很大;病变甚至可能自行消退,因此诊断为II型和III型CAM后应进行一段时间的观察。如果遇到不良预后因素,I型CAM病例建议进行宫内引流。

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