Suppr超能文献

生殖细胞精原细胞瘤

Germ Cell Seminoma

作者信息

Sadiq Qandeel, Khan Farhan A.

机构信息

University of Connecticut

University of Tennessee

Abstract

Germ cell tumors (GCT), derived from primordial germ cells, are a diverse group of neoplasms that arise in the gonads (testicles and ovaries) primarily and may also arise in the anterior mediastinum, pineal gland, and brain. They are clinically classified into two major categories, with significant clinical and prognostic implications: Seminomas and non-seminomas. Seminomas generally have a good prognosis, while non-seminomatous tumors are much more likely to present with metastatic disease as well as mixed germ cell tumors comprising of two or more than two different germ cell tumor components. Although rare, GCT may also arise from extragonadal sites. Term “extragonadal germ cell tumor” (EGGCT) is implied in the absence of any primary gonadal neoplasm and represent 1% to 3% of all GCT. Seminoma constitutes 60% of all primary extragonadal GCT and is seen most notably in midline locations of the body like anterior mediastinum, central nervous system, and retroperitoneum. Seminoma in the retroperitoneum is generally metastatic disease from primary gonadal seminoma unless proven otherwise. In the central nervous system, the pineal gland and suprasellar regions are involved more frequently. Germinoma, an intracranial counterpart of seminoma (extragonadal seminoma), comprises approximately two-third of all intracranial GCT. Germinoma can be pure or mixed (coexisting with other GCT, classified as non-germinomatous GCT). Non-germinomatous GCT makes up the remaining one third, including embryonal carcinoma, yolk sac tumor, choriocarcinomas, teratomas, and mixed tumors (containing more than one histologic element). Less commonly involved sites include paraventricular regions of basal ganglia and thalamus. Very rarely, synchronous involvement of the pineal and the suprasellar region is observed, called bifocal germinoma. Germinoma is more common in young adolescents and is usually diagnosed in the second decade of life. The prognosis is good, with a 5-year survival rate greater than 90% since the tumor is highly radiosensitive.

摘要

生殖细胞肿瘤(GCT)起源于原始生殖细胞,是一组多样的肿瘤,主要发生在性腺(睾丸和卵巢),也可能发生在前纵隔、松果体和脑部。临床上分为两大类,具有重要的临床和预后意义:精原细胞瘤和非精原细胞瘤。精原细胞瘤一般预后良好,而非精原细胞瘤更易出现转移性疾病,以及由两种或两种以上不同生殖细胞肿瘤成分组成的混合性生殖细胞肿瘤。虽然罕见,但GCT也可能起源于性腺外部位。“性腺外生殖细胞肿瘤”(EGGCT)一词指的是在没有任何原发性性腺肿瘤的情况下出现的肿瘤,占所有GCT的1%至3%。精原细胞瘤占所有原发性性腺外GCT的60%,最常见于身体的中线部位,如前纵隔、中枢神经系统和腹膜后。腹膜后的精原细胞瘤通常是原发性性腺精原细胞瘤的转移性疾病,除非另有证实。在中枢神经系统中,松果体和鞍上区域更常受累。生殖细胞瘤是精原细胞瘤(性腺外精原细胞瘤)的颅内对应物,约占所有颅内GCT的三分之二。生殖细胞瘤可以是纯的或混合的(与其他GCT共存,归类为非生殖细胞瘤性GCT)。非生殖细胞瘤性GCT占其余三分之一,包括胚胎癌、卵黄囊瘤、绒毛膜癌、畸胎瘤和混合性肿瘤(包含一种以上组织学成分)。较少受累的部位包括基底神经节和丘脑的脑室旁区域。非常罕见的情况下,会观察到松果体和鞍上区域同时受累,称为双灶性生殖细胞瘤。生殖细胞瘤在青少年中更常见,通常在生命的第二个十年被诊断出来。由于肿瘤对放疗高度敏感,预后良好,5年生存率大于90%。

相似文献

9
Could Aberrant Migration Explain Metachronous Germ Cell Tumors?异常迁移能否解释异时性生殖细胞肿瘤?
Cancer Invest. 2021 Feb;39(2):195-201. doi: 10.1080/07357907.2020.1828447. Epub 2020 Nov 6.

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验