胎儿肺间质瘤:以新一代测序为重点的综合病例研究。

Q4 Medicine
Journal of Chest Surgery Pub Date : 2024-07-05 Epub Date: 2024-02-21 DOI:10.5090/jcs.23.154
Yoo Jin Jung, Seongyeon Jung, Jiwon Koh, Jaemoon Koh, Yoon Kyung Jeon, Sung-Hye Park, Eun Na Kim, Chang Hyun Kang
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引用次数: 0

摘要

胎儿肺间质瘤(FLIT)是一种罕见的呼吸系统肿瘤,其特点是间质细胞未成熟,与妊娠20至24周的胎儿肺实质相似。本研究是韩国首次报道 FLIT。研究还旨在完善FLIT的诊断方法,并通过新一代测序检查无性淋巴瘤受体酪氨酸激酶(无性淋巴瘤激酶)基因重排,提高预后评估的准确性。尽管自2010年首次报道以来,FLIT的初步预后一直很乐观,但某些病理特征与较差的预后相关。因此,准确诊断FLIT对于避免手术切除以外的不必要治疗至关重要。
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: A Comprehensive Case Study with an Emphasis on Next-Generation Sequencing.

Fetal lung interstitial tumor (FLIT), which is characterized by immature interstitial cells resembling the fetal lung parenchyma of 20 to 24 weeks of gestation, is a rare respiratory neoplasm. This study presents the first reported FLIT in Korea. It also aims to refine the diagnostic method of FLIT and increase the accuracy of prognostic assessment by using next-generation sequencing to check for anaplastic lymphoma receptor tyrosine kinase (anaplastic lymphoma kinase) gene rearrangement. Although the initial prognosis for FLIT has been promising since its first report in 2010, certain pathological features are associated with poorer outcomes. Therefore, achieving an accurate diagnosis of FLIT is crucial for avoiding unnecessary treatments beyond surgical resection.

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来源期刊
Journal of Chest Surgery
Journal of Chest Surgery Medicine-Surgery
CiteScore
0.80
自引率
0.00%
发文量
76
审稿时长
7 weeks
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