Suppr超能文献

睾丸多胚瘤:两个在混合性生殖细胞肿瘤中占主导地位的病例报告,并复习性腺多胚瘤。

Polyembryoma of the testis: a report of two cases dominant within mixed germ cell tumors and review of gonadal polyembryomas.

机构信息

Hospital Pathology Associates, Virginia Piper Cancer Institute, Abbott Northwestern Hospital, Minneapolis, MN, USA.

James Homer Wright Pathology Laboratories, Massachusetts General Hospital, Harvard Medical School, Boston, MA, USA.

出版信息

Mod Pathol. 2017 Jul;30(7):908-918. doi: 10.1038/modpathol.2017.25. Epub 2017 Apr 21.

Abstract

Two testicular mixed germ cell tumors, from men of 21 and 41 years, in which polyembryoma predominated are described. A literature review uncovered an additional five testicular and nine ovarian cases. One tumor occurred in a 60-year-old man, but all others occurred within the typical age range of gonadal germ cell tumors. One male presented with gynecomastia and one female with sexual precocity, but all otherwise had standard clinical manifestations. These tumors are typically large with non-specific gross features, but a few have a prominent hemorrhagic appearance. No tumor is known to have been entirely composed of embryoid bodies, the unit upon which the diagnosis of polyembryoma is based. The most common additional germ cell tumor component is teratoma, present in the great majority of cases, with an approximately equal smaller number of tumors being associated with embryonal carcinoma and yolk-sac tumor, manifest as overgrowths of these elements, derived from the parent epithelium within the embryoid body. Rarely there is choriocarcinoma, and syncytiotrophoblast and hepatoid cells are occasionally present. The microscopic features of the tumors vary according to the arrangement of embryoid bodies with other elements, the prominence of associated typically myxoid to edematous stroma, and the degree to which embryoid bodies are perfectly or imperfectly formed. Although its presence in a gonadal mixed germ cell tumor is probably not associated with any special behavior, its unique features should result in polyembryoma being recorded, particularly when present in significant amount. Furthermore, awareness of its features may facilitate recognition, particularly when seen at metastatic sites or extra-gonadal sites of primary germ cell neoplasia. Whether polyembroma should be considered a distinctive pattern of mixed germ cell neoplasia or a particular variant of high-grade immature teratoma is considered, herein, and arguments can be made in favor of each viewpoint.

摘要

描述了 2 例 21 岁和 41 岁男性的睾丸混合性生殖细胞肿瘤,其中以多胚瘤为主。文献复习发现另外还有 5 例睾丸和 9 例卵巢病例。1 例肿瘤发生于 60 岁男性,但所有其他病例均发生于典型的性腺生殖细胞肿瘤年龄范围内。1 例男性表现为男性乳房发育,1 例女性表现为性早熟,但其他所有病例均具有标准的临床表现。这些肿瘤通常较大,具有非特异性的大体特征,但少数具有明显的出血外观。目前还没有已知的肿瘤完全由胚状体组成,而胚状体是多胚瘤诊断的基础。最常见的附加生殖细胞肿瘤成分是畸胎瘤,见于绝大多数病例,少数肿瘤与胚胎癌和卵黄囊瘤相关,表现为这些成分的过度生长,源自胚状体中的母体上皮。罕见绒毛膜癌,偶尔可见合体滋养细胞和肝细胞。肿瘤的显微镜特征根据胚状体与其他成分的排列方式、与典型粘液样至水肿样基质的关联程度以及胚状体的形成程度而有所不同。尽管其在性腺混合性生殖细胞肿瘤中的存在可能与任何特殊行为无关,但由于其独特的特征,应记录为多胚瘤,特别是当大量存在时。此外,认识其特征可能有助于识别,特别是在转移部位或原发性生殖细胞肿瘤的性腺外部位看到时。本文考虑了多胚瘤是否应被认为是混合性生殖细胞肿瘤的一种独特模式或高级未成熟畸胎瘤的一种特殊变体,并可以提出支持每种观点的论据。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验