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细胞的发现:对中间滋养层曲折历史的思考及其本质和病理表现的更新

Discovery of a cell: reflections on the checkered history of intermediate trophoblast and update on its nature and pathologic manifestations.

作者信息

Kurman Robert J, Shih Ie-Ming

机构信息

Departments of Pathology, Gynecology and Obstetrics and Oncology, The Johns Hopkins Medical Institution, Baltimore, Maryland.

出版信息

Int J Gynecol Pathol. 2014 Jul;33(4):339-47. doi: 10.1097/PGP.0000000000000144.

DOI:10.1097/PGP.0000000000000144
PMID:24901393
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4352309/
Abstract

In 1976, a series of 12 cases describing a lesion that had previously not been well characterized was reported as "trophoblastic pseudotumor of the uterus." Up until that time rare reports of the lesion had classified it most often as an unusual type of sarcoma associated with pregnancy. All patients in that series were alive and well except for one who died from complications of a uterine perforation occurring at the time of a diagnostic curettage. Thus, it appeared to be a benign neoplasm but subsequently it was found that some exhibited malignant behavior and the tumor was renamed "placental site trophoblastic tumor." A variety of observations pointed to an origin in a distinctive cell of the placental site, designated "intermediate trophoblast," which physiologically is seen in the normal implantation site. Subsequently, another subset of intermediate trophoblast cells originating from the chorion laeve have been shown to give rise to the placental site nodule/plaque, a well-circumscribed and usually microscopic incidental finding as well as the epithelioid trophoblastic tumor, its putative malignant counterpart. The initial description of "trophoblastic pseudotumor" opened a new area of research which brought to bear immunohistochemical and molecular genetic analyses that eventually has led to new insights in the diverse morphologic changes occurring in early placentation and also led to the development of a new classification of trophoblastic tumors and tumor-like lesions.

摘要

1976年,有一系列12例病例被报道为“子宫滋养细胞假瘤”,该病变此前未得到充分描述。在此之前,关于该病变的罕见报道大多将其归类为与妊娠相关的一种特殊类型的肉瘤。该系列中的所有患者除1例在诊断性刮宫时因子宫穿孔并发症死亡外,其余均存活且状况良好。因此,它似乎是一种良性肿瘤,但后来发现有些表现出恶性行为,该肿瘤被重新命名为“胎盘部位滋养细胞肿瘤”。各种观察结果表明,它起源于胎盘部位一种独特的细胞,即“中间型滋养细胞”,在正常着床部位可见到这种细胞。随后,已证明另一个源自平滑绒毛膜的中间型滋养细胞亚群会形成胎盘部位结节/斑块,这是一种边界清楚且通常为显微镜下偶然发现的病变,以及上皮样滋养细胞肿瘤,它被认为是其恶性对应物。“滋养细胞假瘤”的最初描述开启了一个新的研究领域,引入了免疫组织化学和分子遗传学分析,最终对早期胎盘形成过程中发生的各种形态学变化有了新的认识,也促成了滋养细胞肿瘤和肿瘤样病变新分类的发展。

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本文引用的文献

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Epithelioid trophoblastic tumor: morphological and immunohistochemical study of three lung lesions.上皮样滋养细胞肿瘤:三例肺部病变的形态学和免疫组化研究
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