胎儿肺间质性肿瘤(FLIT):一个病例系列

Q4 Medicine
Kah Ann Ho, N. Fuentes-Bolanos, A. Gifford, A. Jiwane, D. Wanaguru
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引用次数: 2

摘要

背景:胎儿肺间质瘤是一种罕见的良性肺肿瘤。文献中描述了18例FLIT。FLIT的特点是肺部发育停滞,必须与其他预后较差的先天性肺部病变区分开来。病例介绍:我们报告了澳大利亚和新西兰的前两例已知FLIT病例。在这两种情况下,患者在出生时出现呼吸窘迫,需要插管。影像学显示有实体性病变,超声心动图显示有肺动脉高压。患者接受了手术切除,没有任何并发症或复发。结论:FLIT是一种罕见的先天性肺部良性肿瘤,手术切除可有效治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Fetal Lung Interstitial Tumor (FLIT): A case series
Background: Fetal Lung Interstitial Tumor (FLIT) is a rare benign lung tumor. There have been 18 cases of FLIT described in the literature. FLIT is characterized by a region of arrested lung development and must be differentiated from other congenital lung lesions with poorer prognoses. Case Presentation: We report the first two known cases of FLIT in Australia and New Zealand. In both cases, the patients developed respiratory distress at birth requiring intubation. Imaging revealed solid lesions and echocardiography demonstrated pulmonary hypertension. The patients underwent surgical resection without any complications or recurrence. Conclusion: FLIT is a rare benign congenital lung tumor that can be adequately managed with surgical resection.
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来源期刊
Journal of Neonatal Surgery
Journal of Neonatal Surgery Medicine-Surgery
CiteScore
0.30
自引率
0.00%
发文量
29
审稿时长
6 weeks
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