Combined Pre- and Postnatal Minimally Invasive Approach to Complicated Pulmonary Sequestrations.

IF 0.6 Q4 SURGERY European Journal of Pediatric Surgery Reports Pub Date : 2020-01-01 Epub Date: 2020-09-18 DOI:10.1055/s-0040-1713901
Martina Ichino, Francesco Macchini, Anna Morandi, Nicola Persico, Isabella Fabietti, Andrea Zanini, Ernesto Leva
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引用次数: 4

Abstract

Abstract Pulmonary sequestration (PS) is mostly asymptomatic but there is a proportion of fetuses that develop hydrops, leading to fetal or neonatal death. Fetal treatments are available, but postnatal management of the residual lesions is not uniformly defined. We present two cases of combined pre- and postnatal minimally invasive approach to complicated extra-lobar PS. Patient 1 presented with complicated PS at 31 weeks of gestation. Ultrasound-guided laser coagulation of the anomalous artery was successful. The patient was born asymptomatic at 38 weeks. Neonatal magnetic resonance imaging (MRI) showed a residual mass, confirmed by computed tomography (CT) at 6 months. No systemic artery was described, but perfusion was present. We decided for thoracoscopic resection. A residual artery was identified and sealed. Patient 2 presented with complicated PS at 25 weeks of gestation, underwent laser coagulation of the anomalous artery and was born asymptomatic at 38 weeks. Neonatal MRI showed persistence of the lesion, confirmed by CT scan at 4 months. We proceeded with thoracoscopic resection. A residual vessel was ligated. The patients 1 and 2 are now 24 and 21 months old, respectively, and healthy. Prenatal treatment of complicated PS is a life-saving procedure. Postnatal thoracoscopic resection of the residual lesion is feasible and safe; we believe it is the best course of treatment to grant the complete excision of the malformation.

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复杂肺隔离的产前产后联合微创治疗。
肺隔离(PS)大多无症状,但有一部分胎儿出现积水,导致胎儿或新生儿死亡。胎儿治疗是可行的,但产后对残余病变的处理没有统一的定义。我们报告了两例产前和产后联合微创入路治疗复杂的叶外PS。患者1在妊娠31周时出现复杂的PS。超声引导激光凝固异常动脉成功。患者在38周出生时无症状。新生儿核磁共振成像(MRI)显示残留肿块,6个月时通过计算机断层扫描(CT)证实。未见全身动脉,但有灌注。我们决定做胸腔镜切除。发现了一条残留的动脉并将其封闭。患者2在妊娠25周时出现了复杂的PS,对异常动脉进行了激光凝固治疗,38周出生时无症状。新生儿MRI显示病变持续存在,4个月时CT扫描证实。我们进行了胸腔镜切除。结扎了残留的血管。患者1和2现在分别是24个月和21个月,健康。产前治疗复杂的PS是一个挽救生命的过程。产后胸腔镜切除残留病变可行、安全;我们相信完全切除畸形是最好的治疗方法。
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自引率
33.30%
发文量
39
审稿时长
12 weeks
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