Department of Anatomic Pathology, Tohoku University School of Medicine, 2-1 Seiryo-machi, Aoba-ku, Sendai, Miyagi, J 980-8575, Japan.
Personalized Medical Center, Tohoku University Hospital, Sendai, Miyagi, Japan.
Diagn Pathol. 2022 Feb 10;17(1):25. doi: 10.1186/s13000-022-01208-5.
Pulmonary carcinoid tumors rarely coexist with non-small cell lung carcinoma, and only nine cases have been reported previously. The pathogenesis and origin of these combined tumors remain unclear because of its rarity.
We examined two cases of adenocarcinoma coexisting with a typical or atypical carcinoid tumor: Case 1 was a 77-year-old woman and Case 2 was an 83-year-old woman. Both of these cases had no respiratory symptoms, and underwent pulmonary lobectomies due to incidentally detected lung nodules. Recurrence and metastases were not detected after the surgery. Histologically, carcinoid and adenocarcinoma components were present in both cases. The two components coexisted without mixing with each other. Next-generation sequencing was performed on the two components in these cases. In each case, no common genetic variants were detected.
We considered that our cases could histologically and genetically represent collision tumors that did not share common progenitor cells. Comprehensive analyses such as whole genome sequencing could provide important information for elucidating the pathogenesis of adenocarcinoma and carcinoid components.
肺类癌肿瘤很少与非小细胞肺癌共存,此前仅报道过 9 例。由于其罕见性,这些合并肿瘤的发病机制和起源尚不清楚。
我们检查了两例腺癌合并典型或非典型类癌肿瘤的病例:病例 1 为 77 岁女性,病例 2 为 83 岁女性。这两例患者均无呼吸系统症状,因偶然发现的肺结节而行肺叶切除术。手术后未发现复发和转移。组织学上,两例均存在类癌和腺癌成分。两种成分共存,互不混合。对这两例的两个成分进行了下一代测序。在每例中,均未检测到共同的遗传变异。
我们认为我们的病例在组织学和遗传学上可以代表没有共同祖细胞的碰撞肿瘤。全基因组测序等综合分析可为阐明腺癌和类癌成分的发病机制提供重要信息。