Thymic carcinoma recurring 11 years post-extended surgery: a case report.

Kiyoki Okamoto, Takashi Kanou, Sachi Kawagishi, Hideki Nagata, Eiichi Morii, Yasushi Shintani
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Abstract

Background: Thymic carcinoma is a rare type of tumor originating in the thymus, making up about 15-20% of all thymic epithelial tumors. It typically has a poor prognosis, especially in advanced stages, with low 5-year survival rates. Cases where the cancer recurs more than 10 years after surgery are extremely uncommon. Additionally, there are very few reports about the outcomes of patients who undergo aortic resection as part of their treatment for thymic carcinoma.

Case presentation: A 68-year-old male was diagnosed with thymic squamous cell carcinoma classified as Masaoka stage III following the detection of an anterior mediastinal mass during a routine health examination. The patient underwent preoperative treatment, which included two cycles of chemotherapy (cisplatin and docetaxel) and 60 Gy of mediastinal radiotherapy, followed by an extensive surgical procedure comprising extended thymectomy, resection of the ascending aorta and superior vena cava, and wedge resection of the right upper lobe. Postoperative pathological examination revealed ypT3N0M0 disease, corresponding to ypStage IIIa disease, and the patient remained disease-free for 10 years. However, at 11 years after surgery, imaging revealed new nodules in the left lung. Surgical resection confirmed these nodules as metastatic lesions originating from the thymic carcinoma.

Conclusions: This case highlights the critical need for long-term monitoring of thymic carcinoma patients, extending beyond the standard 5-year follow-up due to the potential for late recurrence, even in initially disease-free patients. Furthermore, our findings indicate that aortic resection, when carefully selected, can contribute to favorable long-term outcomes in advanced cases. This report enhances the limited literature on the long-term prognosis of thymic carcinoma, particularly following major vascular resection, and underscores the importance of a multidisciplinary approach to optimize patient management and improve outcomes.

胸腺癌术后11年复发1例。
背景:胸腺癌是一种起源于胸腺的罕见肿瘤,约占所有胸腺上皮肿瘤的15-20%。它通常预后差,特别是在晚期,5年生存率低。手术后10年以上癌症复发的病例极为罕见。此外,很少有关于胸腺癌患者接受主动脉切除术治疗的结果的报道。病例介绍:一名68岁男性,在常规健康检查中发现前纵隔肿块,诊断为胸腺鳞状细胞癌,分类为Masaoka III期。患者接受了术前治疗,包括两个周期的化疗(顺铂和多西他赛)和60 Gy的纵隔放疗,随后进行了广泛的外科手术,包括扩大胸腺切除术、升主动脉和上腔静脉切除术以及右上肺叶楔形切除术。术后病理检查显示为ypT3N0M0病,对应ypiiia期疾病,患者无病10年。然而,在手术后11年,影像学显示左肺有新的结节。手术切除证实这些结节为源自胸腺癌的转移性病变。结论:该病例强调了对胸腺癌患者进行长期监测的迫切需要,由于晚期复发的可能性,即使在最初无疾病的患者中,也要延长标准的5年随访时间。此外,我们的研究结果表明,在精心选择的情况下,主动脉切除术可以为晚期病例带来良好的长期预后。本报告加强了关于胸腺癌长期预后的有限文献,特别是在大血管切除术后,并强调了多学科方法优化患者管理和改善预后的重要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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