Unusual Synchronous Multiple Primary Early-Stage Lung Adenocarcinoma with Concomitant MET Exon 14 Skipping, PIK3CA and KRAS Mutations: A Case Report.

IF 0.7 Q4 ONCOLOGY Case Reports in Oncology Pub Date : 2024-08-07 eCollection Date: 2024-01-01 DOI:10.1159/000540355
Yongjing Zhang, Qiqi Gao
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Abstract

Instruction: Synchronous multiple primary lung cancer (sMPLC) constitutes a distinct subtype of NSCLC, where accurate diagnosis and prognostic evaluation remain challenging.

Case presentation: The case involves a 70-year-old male patient admitted to the hospital due to bilateral pulmonary nodules. The patient underwent staged resection. Molecular pathological examination revealed that tumor A harbored concurrent mutations in MET exon 14 skipping and PIK3CA (p.E545K), while tumor B exhibited a KRAS exon 2 (p.G12S/D) mutation. Postoperatively, the patient demonstrated a favorable recovery, with no evidence of recurrence for 1 year.

Conclusion: This study presents a case of sMPLC in early-stage lung cancer, illustrating the genetic heterogeneity in early-stage lung adenocarcinoma and underscoring the significance of precise evaluation of sMPLC and intrapulmonary metastases.

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非同寻常的多发性同步原发性早期肺腺癌同时伴有 MET 第 14 号外显子跳越、PIK3CA 和 KRAS 突变:病例报告。
说明:同步多原发肺癌(sMPLC)是 NSCLC 的一个独特亚型,其准确诊断和预后评估仍具有挑战性:病例涉及一名 70 岁男性患者,因双侧肺结节入院。患者接受了分期切除术。分子病理学检查显示,肿瘤 A 同时存在 MET 14 号外显子跳变和 PIK3CA(p.E545K)突变,而肿瘤 B 则显示 KRAS 2 号外显子(p.G12S/D)突变。术后,患者恢复良好,一年内无复发迹象:本研究介绍了一例早期肺癌 sMPLC 病例,说明了早期肺腺癌的遗传异质性,并强调了精确评估 sMPLC 和肺内转移的重要性。
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来源期刊
CiteScore
1.40
自引率
12.50%
发文量
151
审稿时长
7 weeks
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