Clinical and Pathological Characteristics and Prognosis of Lung Adenocarcinoma With High-Grade Fetal Features: A Retrospective Analysis

被引:1
作者
Gu, Yumei [1 ]
Zhang, Shu [2 ,3 ]
Liang, Xiaolong [1 ]
Zhao, Hongying [1 ]
Li, Xue [1 ]
Lu, Jun [1 ]
机构
[1] Capital Med Univ, Beijing Chao Yang Hosp, Dept Pathol, 8 Gong Ren Ti Yu Chang South Rd, Beijing 100020, Peoples R China
[2] Capital Med Univ, Beijing Inst Resp Med, Dept Resp & Crit Care Med, Beijing, Peoples R China
[3] Capital Med Univ, Beijing Chao Yang Hosp, Beijing, Peoples R China
关键词
fetal adenocarcinoma of the lung; pathological characteristics; clinical features; radiological characteristics; prognosis; INTERNATIONAL MULTIDISCIPLINARY CLASSIFICATION; WNT SIGNALING PATHWAY; BETA-CATENIN; TUMOR; DIFFERENTIATION; ASSOCIATION; ASPIRATION;
D O I
10.1177/10668969231188890
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Fetal adenocarcinoma of the lung is a rare tumor. The clinical and pathological characteristics, treatment, and prognosis of patients with lung adenocarcinoma with fetal lung-like morphology were retrospectively investigated. The tumors of 9 patients with lung adenocarcinoma contained fetal lung-like morphology. One patient had pure-type high-grade fetal adenocarcinoma. Two patients had more than 50% high-grade fetal adenocarcinoma. Six specimens accounted for < 50% of the high-grade fetal features. It occurred in 7 men and 2 women. The median age at diagnosis was 62.0 years. Thyroid transcription factor-1 was frequently expressed in 8 specimens. All 9 specimens showed high rates of immunopositivity for & beta;-catenin and E-cadherin. Three specimens showed nuclear & beta;-catenin staining. Some patients showed immune expression of CDX2, & alpha;-fetoprotein (AFP), SALL4, and Glypican-3. Three of these specimens were diffusely strongly positive for p53, including 1 mixed-type high-grade fetal adenocarcinoma and 2 lung adenocarcinomas with high-grade fetal features. However, the other 6 patients had wild-type p53, including 1 pure-type high-grade fetal adenocarcinoma. PD-L1 was not expressed in all patients. Epidermal growth factor receptor mutations were detected in 1 patient. All patients were diagnosed using surgical samples. During the follow-up period of 36 months (range: 1-92 months), 3 patients received chemotherapy. One patient underwent radiotherapy. Two patients experienced recurrences. No patient died. PD-L1 expression status suggests a poor response to immune checkpoint therapy. The prognosis of the patient was relatively good.
引用
收藏
页码:667 / 678
页数:12
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