Chu Benjamin, Huang Jiaoti
Department of Pathology, Duke University Hospital, Durham, North Carolina, USA.
Int J Surg Pathol. 2025 Dec;33(8):1829-1832. doi: 10.1177/10668969251343220. Epub 2025 May 30.
Testicular germ cell tumors represent less than 1% of all cancer diagnoses in men. Postpubertal-type teratomas are a form of nonseminomatous germ cell tumor derived from 2 or more embryonic germ cell layers. Rarely, these tumors have been shown to develop somatic-type malignancy, where a nongerm cell malignancy such as carcinoma or sarcoma arises in a germ cell tumor. Neuroendocrine tumors as a somatic-type malignancy in teratomas are extremely rare. Here, we report a high-grade neuroendocrine tumor arising within a metastatic teratoma in a 25-year-old man.
睾丸生殖细胞肿瘤在男性所有癌症诊断病例中占比不到1%。青春期后型畸胎瘤是一种非精原细胞性生殖细胞肿瘤,起源于两个或更多胚胎生殖细胞层。这些肿瘤很少会发展为体细胞型恶性肿瘤,即生殖细胞肿瘤中出现非生殖细胞恶性肿瘤,如癌或肉瘤。神经内分泌肿瘤作为畸胎瘤中的体细胞型恶性肿瘤极为罕见。在此,我们报告一例发生在一名25岁男性转移性畸胎瘤内的高级别神经内分泌肿瘤。