High-grade Endometrial Endometrioid Carcinoma: A Case Report of Complete Transdifferentiation to Pilomatrix-like Carcinoma.

IF 1 4区 医学 Q4 PATHOLOGY
Gabriela Patrichi, Andrei Patrichi, Andrea Palicelli, Thais Maloberti, Dario de Biase, Robert Soslow, Simona Stolnicu
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引用次数: 0

Abstract

IntroductionEndometrial endometrioid carcinomas can show multiple lines of differentiation, including pilomatrix-like high-grade endometrioid carcinoma, a recently described tumor with similarity to cutaneous pilomatrix carcinoma and associated with very aggressive clinical behavior.MethodsWe present a 56-year-old woman with an endometrial tumor associated with secondary involvement of both ovaries, left tubo-ovarian ligament and obturator lymph nodes. The diagnosis of high-grade endometrioid carcinoma in a previously performed curettage was confirmed in the hysterectomy specimen.ResultsMicroscopically, the tumor exhibited a solid, nested/insular pattern with basaloid cells, predominantly seen at the periphery, ghost cell keratinization towards the center of the nests, and extensive geographic necrosis. No low-grade endometrioid carcinoma component was identified throughout the primary tumor or metastases after extensive sampling. Immunohistochemical assessment showed aberrant cytoplasmic and nuclear expression of β-catenin, and focal CDX2 expression. Tumor cells were negative for PAX8, and estrogen and progesterone receptors (ER/PR). The next-generation sequencing (NGS) analysis found a CTNNB1 pathogenic mutation (p.Ser37Phe, c.110C > T; variant allele frequency: 18.6%). Based on these morphologic, immunohistochemistry and NGS analysis, a diagnosis of pilomatrix-like high-grade endometrioid carcinoma was established.ConclusionThe absence of a low-grade endometrioid carcinoma component makes this pilomatrix-like high-grade endometrioid carcinoma, a very rare tumor, even more special. This and the absence of PAX8 and ER/PR expression in an unusual morphological context proved to be diagnostically challenging. This patient's presentation at high stage is concordant with the literature's description of this tumor as aggressive. It is not yet known whether standard adjuvant therapies for high-risk endometrial carcinomas are effective.

高级别子宫内膜子宫内膜样癌:完全转分化为毛基质样癌1例。
子宫内膜样癌可表现为多种分化,包括毛基质样高级别子宫内膜样癌,这是一种最近发现的与皮肤毛基质癌相似的肿瘤,具有非常侵袭性的临床行为。方法我们报告一位56岁的女性子宫内膜肿瘤伴继发性累及双卵巢、左侧输卵管卵巢韧带和闭孔淋巴结。高级别子宫内膜样癌的诊断在以前进行的刮除是在子宫切除术标本证实。结果显微镜下,肿瘤呈坚实的巢状/岛状,基底样细胞主要分布在周围,巢中心的鬼细胞角化,广泛的地理坏死。在广泛取样后,未发现原发性或转移性低级别子宫内膜样癌成分。免疫组化检查显示β-catenin和CDX2的细胞质和细胞核表达异常。肿瘤细胞PAX8、雌激素和孕激素受体(ER/PR)均为阴性。新一代测序(NGS)分析发现CTNNB1致病性突变(p.Ser37Phe, c.110C > T;变异等位基因频率:18.6%)。基于形态学、免疫组化和NGS分析,诊断为毛基质样高级别子宫内膜样癌。结论由于低级别子宫内膜样癌成分的缺失,使得本病例作为一种非常罕见的恶性肿瘤,显得更加特殊。这和PAX8和ER/PR表达的缺失在不寻常的形态学背景下被证明是诊断上的挑战。该患者在晚期的表现与文献中对肿瘤侵袭性的描述一致。目前尚不清楚标准辅助治疗对高危子宫内膜癌是否有效。
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来源期刊
CiteScore
2.10
自引率
0.00%
发文量
198
审稿时长
1 months
期刊介绍: International Journal of Surgical Pathology (IJSP) is a peer-reviewed journal published eight times a year, which offers original research and observations covering all major organ systems, timely reviews of new techniques and procedures, discussions of controversies in surgical pathology, case reports, and images in pathology. This journal is a member of the Committee on Publication Ethics (COPE).
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