Wang Zongyu, Xu Chang, He Taozhen, Yuan Miao
West China Hospital, Sichuan University, Chengdu, China.
Front Pediatr. 2023 Feb 10;10:1045037. doi: 10.3389/fped.2022.1045037. eCollection 2022.
The patient was a male neonate, and a prenatal ultrasound had detected a right lung mass. He was born at term and after delivery had tachypnea and feeding difficulties. A chest x-ray and a computed tomography (CT) scan revealed a large mass in the right chest with compression on the right lung after birth. We initially considered congenital pulmonary airway malformation (CPAM). After conservative treatment, his respiratory symptoms worsened gradually, and he required continuous supplemental oxygen. The symptoms could not be relieved by puncturing due to a postnatal ultrasound having shown a mass with anechoic microcystic spaces. He therefore underwent an emergency thoracotomy and lobectomy at 14 days of age. The pathology was consistent with fetal lung interstitial tumor (FLIT). The patient remained healthy at the three-month follow-up. We reviewed the literature on FLIT and found that, to date, 23 cases have been reported worldwide.
该患者为男性新生儿,产前超声检查发现右肺有一肿块。他足月出生,出生后出现呼吸急促和喂养困难。胸部X线和计算机断层扫描(CT)显示右胸有一个大肿块,出生后对右肺产生压迫。我们最初考虑为先天性肺气道畸形(CPAM)。经过保守治疗,他的呼吸道症状逐渐恶化,需要持续补充氧气。由于产后超声显示肿块有微囊无回声区,穿刺无法缓解症状。因此,他在14日龄时接受了紧急开胸手术和肺叶切除术。病理结果与胎儿肺间质瘤(FLIT)相符。患者在三个月的随访中保持健康。我们查阅了关于FLIT的文献,发现迄今为止,全球已报道23例。