Embryoid Bodies and Related Proliferations in Ovarian Germ Cell Tumors.

IF 4.5 1区 医学 Q1 PATHOLOGY American Journal of Surgical Pathology Pub Date : 2024-09-01 Epub Date: 2024-07-04 DOI:10.1097/PAS.0000000000002261
Kyle M Devins, Robert H Young
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Abstract

We investigated the frequency and associated pathology of embryoid bodies in ovarian tumors by evaluating neoplasms in which they are known to occur: 100 immature teratomas, 125 malignant mixed germ cell tumors, and 6 polyembryomas. Three immature teratomas contained a single relatively well-formed embryoid body, whereas these and 11 others showed foci we categorized as embryoid body remnants consisting of microscopic aggregates of embryonal or yolk sac-type epithelium associated with spaces consistent with yolk sac or amniotic cavity but lacking a classic embryoid body structure. Teratomas with these foci were all high grade. A well-formed embryoid body was found in only 1 malignant mixed tumor, but embryoid body remnants were present in 25%, invariably associated with foci of immature teratoma (100%) and often with yolk sac tumor (97%), embryonal carcinoma (35%), or both (32%). These foci usually took the form of round to oval aggregates, often well-circumscribed, for which the term "polyembryoma background" has been proposed. The polyembryomas were typically grossly hemorrhagic and occurred in patients from 9 to 43 years of age. The embryoid bodies in them generally grew in lobules within an edematous to occasionally myxoid stroma. Four tumors contained liver-like cells, 4 numerous glands likely recapitulating the allantois, 3 syncytiotrophoblast cells, 2 prominent cysts, and 2 striking vascular proliferations. This study indicates that (1) typical embryoid bodies are rare in immature teratomas but about 14% of them have embryoid body remnants. (2) Embryoid body remnants are seen in 25% of malignant mixed germ cell tumors with a teratomatous component and often proliferate to form yolk sac tumor and embryonal carcinoma. (3) Well-formed embryoid bodies growing in a confluent manner (polyembryoma) are rare, and minor foci of teratoma, yolk sac tumor, or embryonal carcinoma are almost always present, indicating that these are fundamentally malignant mixed germ cell tumors but the polyembryoma component is dominant and distinctive which, in our opinion, justifies its own nomenclature. (4) Embryoid bodies are not a feature of other germ cell tumors.

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卵巢生殖细胞瘤中的类胚胎体及相关增殖现象
我们通过评估已知存在胚状体的肿瘤,研究了胚状体在卵巢肿瘤中的出现频率和相关病理:其中包括 100 个未成熟畸胎瘤、125 个恶性混合生殖细胞瘤和 6 个多胚胎瘤。3 个未成熟畸胎瘤含有一个相对成型的类胚体,而这 3 个畸胎瘤和另外 11 个畸胎瘤出现的病灶被我们归类为类胚体残余,包括胚胎或卵黄囊型上皮的微小聚集,与卵黄囊或羊膜腔的空间一致,但缺乏典型的类胚体结构。带有这些病灶的畸胎瘤均为高级别。仅在 1 例恶性混合瘤中发现了形态完好的类胚体,但有 25% 的混合瘤中存在类胚体残余,它们无一例外地与未成熟畸胎瘤病灶(100%)相关,而且往往与卵黄囊肿瘤(97%)、胚胎癌(35%)或两者(32%)相关。这些病灶通常呈圆形至椭圆形聚集,通常具有良好的环状结构,因此被称为 "多胚胎瘤背景"。多胚胎瘤通常会严重出血,发生在 9 至 43 岁的患者身上。其中的胚状体一般呈小叶状生长在水肿或偶见肌样基质中。其中 4 个肿瘤含有肝样细胞,4 个肿瘤中的大量腺体可能再现了尿囊,3 个肿瘤中含有合胞滋养细胞,2 个肿瘤中含有突出的囊肿,2 个肿瘤中含有明显的血管增生。这项研究表明:(1) 典型的类胚体在未成熟畸胎瘤中很少见,但其中约 14% 有类胚体残余。(2)25%的恶性混合生殖细胞瘤中可见胚状体残余,其中有畸胎瘤成分,并经常增殖形成卵黄囊瘤和胚胎癌。(3) 以汇合方式生长的形态良好的类胚体(多胚瘤)很少见,而且几乎总是存在畸胎瘤、卵黄囊瘤或胚胎癌的小病灶,这表明这些肿瘤从根本上说是恶性混合生殖细胞瘤,但多胚瘤成分占主导地位,且具有独特性,我们认为有理由将其命名为多胚瘤。(4) 类胚胎体不是其他生殖细胞瘤的特征。
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来源期刊
CiteScore
10.30
自引率
5.40%
发文量
295
审稿时长
1 months
期刊介绍: The American Journal of Surgical Pathology has achieved worldwide recognition for its outstanding coverage of the state of the art in human surgical pathology. In each monthly issue, experts present original articles, review articles, detailed case reports, and special features, enhanced by superb illustrations. Coverage encompasses technical methods, diagnostic aids, and frozen-section diagnosis, in addition to detailed pathologic studies of a wide range of disease entities. Official Journal of The Arthur Purdy Stout Society of Surgical Pathologists and The Gastrointestinal Pathology Society.
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