Neuroendocrine Tumor as a Somatic-Type Malignancy in Metastatic Teratoma.

IF 0.9 4区 医学 Q4 PATHOLOGY
Benjamin Chu, Jiaoti Huang
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引用次数: 0

Abstract

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.

神经内分泌肿瘤作为转移性畸胎瘤的躯体型恶性肿瘤。
睾丸生殖细胞肿瘤在男性所有癌症诊断中所占比例不到1%。青春期后型畸胎瘤是一种源自2个或更多胚胎生殖细胞层的非半细胞性生殖细胞肿瘤。很少,这些肿瘤已被证明发展为躯体型恶性肿瘤,其中非生殖细胞恶性肿瘤,如癌或肉瘤出现在生殖细胞肿瘤。神经内分泌肿瘤作为畸胎瘤的躯体型恶性肿瘤极为罕见。在此,我们报告一例发生在25岁男性转移性畸胎瘤内的高度神经内分泌肿瘤。
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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来源期刊
CiteScore
2.10
自引率
0.00%
发文量
198
审稿时长
1 months
期刊介绍: International Journal of Surgical Pathology (IJSP) is a peer-reviewed journal published eight times a year, which offers original research and observations covering all major organ systems, timely reviews of new techniques and procedures, discussions of controversies in surgical pathology, case reports, and images in pathology. This journal is a member of the Committee on Publication Ethics (COPE).
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