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原发性睾丸神经内分泌肿瘤伴肝淋巴结转移:一例报告并文献复习

Primary testicular neuroendocrine tumor with liver lymph node metastasis: A case report and review of the literature.

作者信息

Xiao Tong, Luo Long-Hua, Guo Liang-Fei, Wang Li-Qin, Feng Liang

机构信息

Department of Urology, The First Affiliated Hospital of Nanchang University, Nanchang 330006, Jiangxi Province, China.

出版信息

World J Clin Cases. 2022 Nov 16;10(32):12028-12035. doi: 10.12998/wjcc.v10.i32.12028.

Abstract

BACKGROUND

Primary testicular neuroendocrine tumors (TNETs) are sporadic, accounting for only 0.23% of all testicular tumors. Few cases have been reported in the literature, and no uniform treatment protocol exists. We report a case of a primary TNET with liver lymph node metastasis diagnosed at the age of 24 years and discuss its clinicopathological features, diagnosis, differential diagnosis, treatment, and prognosis.

CASE SUMMARY

We report the case of a 24-year-old patient with a primary TNET with liver lymph node metastasis. The patient was found to have a right testicular swelling of about 3 cm × 4 cm in size with unclear borders and no testicular pressure pain seven years ago without any examination or treatment. One month ago, an ultrasound examination was performed for persistent enlargement of the right testis, which showed an occupying lesion of the right testis approximately 110 mm × 102 mm × 82 mm in size. Magnetic resonance imaging scan of the testis (plain scan) showed that the right testis was an occupying lesion with inhomogeneous density and mixed signal, the boundary was still clear, and the possibility of seminoma was considered; chest X-ray and computed tomography did not show any apparent abnormalities. The patient underwent radical orchiectomy, and the pathological examination suggested a right TNET with a typical carcinoid tumor histological type. One month after the surgery, the patient received nine cycles of lanreotide chemotherapy at a dose of 90 mg/mo without adverse effects. No distant lymph node or other organ metastases were detected at follow-up. He is in good physical condition and attends regular follow-up visits.

CONCLUSION

Neuroendocrine tumors are rare in clinical practice, and the diagnosis mainly relies on the characteristics of microscopic tumor cells and immunohistochemical features. Treatment involves radical orchiectomy. If it is accompanied by distant lymph node metastasis and the metastatic lesion can be resected, it should be surgically removed; if it cannot be resected, growth inhibitor analog octreotide or lanreotide chemotherapy can be administered to obtain good results, with close postoperative follow-up to prevent recurrence and metastasis.

摘要

背景

原发性睾丸神经内分泌肿瘤(TNETs)较为散发性,仅占所有睾丸肿瘤的0.23%。文献报道的病例较少,且尚无统一的治疗方案。我们报告一例24岁诊断为原发性TNET伴肝淋巴结转移的病例,并讨论其临床病理特征、诊断、鉴别诊断、治疗及预后。

病例摘要

我们报告一例24岁原发性TNET伴肝淋巴结转移的患者。该患者7年前被发现右侧睾丸肿大,大小约3cm×4cm,边界不清,无睾丸压痛,未进行任何检查及治疗。1个月前,因右侧睾丸持续增大行超声检查,结果显示右侧睾丸有一大小约110mm×102mm×82mm的占位性病变。睾丸磁共振成像扫描(平扫)显示右侧睾丸为占位性病变,密度不均匀,信号混合,边界尚清,考虑精原细胞瘤可能性大;胸部X线及计算机断层扫描未显示任何明显异常。患者接受了根治性睾丸切除术,病理检查提示右侧TNET,组织学类型为典型类癌肿瘤。术后1个月,患者接受了9个周期的兰瑞肽化疗,剂量为90mg/月,未出现不良反应。随访未发现远处淋巴结或其他器官转移。患者身体状况良好,定期复诊。

结论

神经内分泌肿瘤在临床实践中较为罕见,诊断主要依靠肿瘤细胞的微观特征及免疫组化特征。治疗包括根治性睾丸切除术。若伴有远处淋巴结转移且转移灶可切除,则应手术切除;若无法切除,可给予生长抑素类似物奥曲肽或兰瑞肽化疗,以取得良好效果,并在术后密切随访以预防复发和转移。

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