Pilomatrix-like High-grade Endometrial Carcinoma: An Underdiagnosed Entity With Aggressive Clinicopathologic Features.

IF 4.5 1区 医学 Q1 PATHOLOGY
Feng Zhou, Lei Qin, Suming Huang, Wanrun Lin, Huijuan Zhang, Vinita Parkash, Wenxin Zheng
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引用次数: 0

Abstract

Pilomatrix-like high-grade endometrial carcinoma (PiMHEC) is a rare and aggressive variant of endometrial carcinoma often misdiagnosed due to overlapping features with other high-grade malignancies. This study characterizes its clinicopathologic, immunophenotypic, and molecular features to establish key diagnostic criteria and propose a standardized terminology. Ten tumors were analyzed using histopathologic examination, immunohistochemistry, and next-generation sequencing. All but 1 tumor exhibited both low-grade endometrioid and high-grade basaloid components, the latter characterized by either geographic or comedo-type necrosis and shadow cells. Although shadow cells are a hallmark feature, they may be focal or absent, necessitating careful evaluation. High-grade areas consistently showed ER and PR negativity with diffuse nuclear β-catenin staining, correlating with CTNNB1 exon 3 mutations in all tumors. Identical CTNNB1 mutations in spatially distinct tumor components suggest a clonal progression from a low-grade precursor. Additional mutations in ARID1A, PTEN, and PIK3CA were identified. Clinically, PiMHEC exhibited aggressive behavior, with 7 patients experiencing recurrence and 1 succumbing to the disease within 9 months. Metastatic sites included the lungs, liver, lymph nodes, and abdominal wall. PD-L1 expression in 4 tumors suggests potential responsiveness to immune checkpoint inhibitors, whereas low-level HER2 expression (1+ to 2+) in 5 tumors raises the possibility of HER2-targeted therapies. Folate receptor alpha was not expressed in any tumor. In conclusion, PiMHEC is a distinct and highly aggressive endometrial carcinoma with unique histopathologic and molecular features that differentiate it from high-grade endometrioid and other high-grade endometrial cancers including squamous cell carcinoma in rare situations. Its key diagnostic features include high-grade basaloid tumor cells associated with shadow cells, tumor necrosis, and diffuse nuclear β-catenin staining. To improve diagnostic accuracy and reduce ambiguity, we propose adopting "pilomatrix-like high-grade endometrial carcinoma" as a standardized term.

毛基质样高级别子宫内膜癌:具有侵袭性临床病理特征的未确诊实体。
毛基质样高级别子宫内膜癌(PiMHEC)是一种罕见的侵袭性子宫内膜癌,因其与其他高级别恶性肿瘤的特征重叠而常被误诊。本研究分析其临床病理、免疫表型和分子特征,建立关键诊断标准,并提出标准化术语。采用组织病理学检查、免疫组织化学和下一代测序对10例肿瘤进行分析。除1例外,所有肿瘤均表现为低级别子宫内膜样和高级别基底细胞样成分,后者表现为地理型或喜剧型坏死和阴影细胞。虽然阴影细胞是一个标志性的特征,但它们可能是局部的或不存在的,需要仔细评估。高级别区域一致显示ER和PR阴性,弥漫性核β-catenin染色,与所有肿瘤中CTNNB1外显子3突变相关。在空间上不同的肿瘤成分中相同的CTNNB1突变提示低级别前体的克隆进展。另外还发现了ARID1A、PTEN和PIK3CA的突变。临床上,PiMHEC表现出侵袭性行为,7例复发,1例在9个月内死亡。转移部位包括肺、肝、淋巴结和腹壁。4例肿瘤中PD-L1的表达提示对免疫检查点抑制剂的潜在反应,而5例肿瘤中HER2的低水平表达(1+至2+)提高了HER2靶向治疗的可能性。叶酸受体α在所有肿瘤中均未表达。总之,PiMHEC是一种独特的高侵袭性子宫内膜癌,具有独特的组织病理学和分子特征,将其与高级别子宫内膜样癌和其他罕见的高级别子宫内膜癌(包括鳞状细胞癌)区分开来。其主要诊断特征包括高级别基底细胞样肿瘤细胞伴阴影细胞、肿瘤坏死和弥漫性核β-catenin染色。为了提高诊断的准确性和减少歧义,我们建议采用“毛基质样高级别子宫内膜癌”作为标准化术语。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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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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