Cavoretto P, Molina F, Poggi S, Davenport M, Nicolaides K H
Department of Fetal Medicine, King's College Hospital, London, UK.
Ultrasound Obstet Gynecol. 2008 Nov;32(6):769-83. doi: 10.1002/uog.6218.
To describe the antenatal findings and outcome of fetuses with echogenic lung lesions.
This was a retrospective study of the prenatal sonographic features, antenatal management and outcome of 193 fetuses with an echogenic lung lesion diagnosed at 18-35 weeks of gestation. There were nine cases of congenital high airway obstruction syndrome (CHAOS), 170 cases of cystic adenomatoid malformation (CAM) and 14 cases of pulmonary sequestration (PS). A literature search was also carried out to compare our data with those of previous series.
The prognosis in our series of fetuses with CHAOS was invariably poor, but the literature describes a handful of survivors after delivery by Cesarean section and ex-utero intrapartum therapy (EXIT). Of the cases in our series with PS and no pleural effusions, more than 95% survived; in half of these cases the lesion resolved antenatally and in the other half sequestrectomy was carried out postnatally. In cases with PS and pleural effusions, successful treatment was provided by the placement of thoracoamniotic shunts or occlusion of the feeding blood vessel by ultrasound-guided laser coagulation or injection of sclerosants. In cases with CAM and no hydrops, there was more than 95% survival and in up to half of the cases there was sonographic evidence of spontaneous antenatal resolution of the hyperechogenic lesion, which was confirmed by postnatal imaging in about 60% of the cases. Of the cases with CAM with hydrops managed expectantly, more than 95% died before or after birth. Of the cases with macrocystic CAM with hydrops, two-thirds survived after placement of a thoracoamniotic shunt. In cases with microcystic CAM with hydrops, there is some evidence that open fetal surgery with lobectomy could improve survival but such treatment is highly invasive for the mother.
CHAOS is a severe abnormality, whereas CAM and PS are associated with a good prognosis. In a high proportion of fetuses with hyperechogenic lung lesion, there is spontaneous antenatal resolution and the underlying pathology may be transient bronchial obstruction.
描述肺回声增强性病变胎儿的产前检查结果及结局。
这是一项回顾性研究,纳入了193例在妊娠18 - 35周时诊断为肺回声增强性病变的胎儿,分析其产前超声特征、产前管理及结局。其中先天性高位气道梗阻综合征(CHAOS)9例,囊性腺瘤样畸形(CAM)170例,肺隔离症(PS)14例。同时进行文献检索,以将我们的数据与既往系列研究的数据进行比较。
我们系列中CHAOS胎儿的预后通常较差,但文献报道有少数经剖宫产和产时宫外治疗(EXIT)后存活的病例。在我们系列中无胸腔积液的PS病例中,超过95%存活;其中一半病例病变在产前自行消退,另一半在出生后行肺叶切除术。对于有胸腔积液的PS病例,通过放置胸腔羊膜分流管或超声引导下激光凝固喂养血管或注射硬化剂成功进行了治疗。对于无水肿的CAM病例,存活率超过95%,高达一半的病例有超声证据表明产前高回声病变自发消退,约60%的病例经产后影像学检查证实。对于期待治疗的有水肿的CAM病例,超过95%在出生前或出生后死亡。对于有水肿的大囊型CAM病例,放置胸腔羊膜分流管后三分之二存活。对于有水肿的微囊型CAM病例,有证据表明开放性胎儿肺叶切除术可能提高存活率,但这种治疗对母亲具有高度侵袭性。
CHAOS是一种严重异常,而CAM和PS预后良好。在高比例的肺回声增强性病变胎儿中,存在产前自发消退,其潜在病理可能是短暂性支气管阻塞。