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原发性卵巢黏液性肿瘤中缺乏并发成熟畸胎瘤的阑尾样形态:4例系列病例展示STR分析的应用价值

Appendix-like morphology in primary ovarian mucinous tumors lacking a concurrent mature teratoma: A series of 4 cases illustrating the utility of STR analysis.

作者信息

Yang Xiaoyan, Rehrauer William M, Weisman Paul S, Xu Jin

机构信息

Department of Pathology and Laboratory Medicine, University of Wisconsin-Madison School of Medicine and Public Health, Madison, WI, United States of America.

Department of Pathology and Laboratory Medicine, University of Wisconsin-Madison School of Medicine and Public Health, Madison, WI, United States of America.

出版信息

Ann Diagn Pathol. 2025 Dec;79:152532. doi: 10.1016/j.anndiagpath.2025.152532. Epub 2025 Jul 13.

DOI:10.1016/j.anndiagpath.2025.152532
PMID:40680701
Abstract

Recently in this journal, Ramalingam et al described the clinicopathological features of mucinous ovarian tumors arising in association with mature cystic teratomas (MT). Of particular interest to us are the appendix-like histological features including prominent subepithelial stromal clefts and pseudomyxoma ovarii described by Ramalingam et al and others. In our own practice, we have encountered a handful of mucinous ovarian tumors with the above-noted histological features for which no MT and no appendiceal tumor could be found, leaving the tumors' origin in question. Here we share our experience using short tandem repeat (STR) analysis in order to address this very scenario using 4 illustrative cases. Using STR analysis, we show that the above-noted histological features may indeed suggest a teratomatous origin even in the absence of a histologically apparent MT. We also show that these same histological features may be seen in bona fide primary ovarian mucinous tumors that have a purely somatic origin.

摘要

最近,Ramalingam等人在本杂志上描述了与成熟囊性畸胎瘤(MT)相关的黏液性卵巢肿瘤的临床病理特征。Ramalingam等人及其他研究者所描述的类似阑尾的组织学特征,包括显著的上皮下间质裂隙和卵巢假黏液瘤,特别引起了我们的关注。在我们自己的临床实践中,我们遇到了一些具有上述组织学特征的黏液性卵巢肿瘤,在这些肿瘤中未发现MT和阑尾肿瘤,这使得肿瘤的起源成谜。在此,我们分享使用短串联重复序列(STR)分析的经验,通过4个实例来解决这一情况。通过STR分析,我们表明,即使在没有组织学上明显的MT的情况下,上述组织学特征也可能确实提示畸胎瘤起源。我们还表明,在具有纯体细胞起源的真正原发性卵巢黏液性肿瘤中也可能出现这些相同的组织学特征。

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