乳腺多形性分叶状癌转移至膀胱:10例报告及TRPS1与浆液性尿路上皮癌的鉴别诊断评估。

Guan-Nan Zhang, Barbara Susnik, Emma J Paulsen, Lisa L Lyons, Katiana S Delma, Merce Jorda, Jonathan I Epstein, Oleksandr N Kryvenko
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引用次数: 0

摘要

背景膀胱转移性多形性小叶癌(MPLC)非常罕见,其组织学和免疫组化与浆细胞性尿路上皮癌(PUC)有相当大的重叠:目的:从形态学和免疫组化方面区分膀胱浆细胞性尿路上皮癌(MPLC)和浆细胞性尿路上皮癌(PUC),包括一种新的标记物TRPS1:对 10 例膀胱 MPLC 进行重新评估,并用雌激素、孕激素和雄激素受体、GATA3、角蛋白 5/6、HMWK、GCDFP-15 和 TRPS1 进行染色。16 例 PUC 构成对照组:我们研究了 4 例经尿道切除的膀胱肿瘤和 6 例活检组织,这些组织来自平均 15 年前患过乳腺癌的 10 名妇女(中位年龄 69 岁)。显微镜下的肿瘤形态包括单细胞和细胞束(4 例)、巢状/片状粘连细胞(2 例)或两者兼有(4 例)。所有肿瘤的细胞都有大量嗜酸性细胞质和模仿 PUC 的偏心核,10 个肿瘤中有 7 个有印戒细胞。MPLC的雌激素受体(10个中有8个)、孕激素受体(7个中有3个)和雄激素受体(10个中有4个);GCDFP-15(10个中有7个);GATA3(10个中有9个);HMWK(8个中有7个);TRPS1(10个中有7个)均呈阳性。没有 MPLCs 染色角蛋白 5/6(n = 9)。在 16 个 PUC 中,2 个显示出微弱的 TRSP1 染色,2 个显示出强烈的 TRSP1 染色;16 个 PUC 中,7 个 p63 阴性:结论:膀胱MPLC常出现在有远期乳腺癌病史的患者中,在组织学和免疫组化方面与PUC有明显的重叠。根据之前的研究和本次研究,雌激素受体(尤其是 SP-1)、乳腺球蛋白和 p63 有助于区分 MPLC 和 PUC。角蛋白 5/6 可能有助于区分较少见的基底型 PUC,因为它在 MPLC 中通常呈阴性。有些 PUC 表达 TRPS1。由于这些肿瘤的免疫表型有很大的重叠,因此应谨慎从事,否则会造成严重的分类错误。
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Metastatic Pleomorphic Lobular Carcinoma of the Breast to the Urinary Bladder: A Report of 10 Cases and Assessment of TRPS1 in the Differential Diagnosis With Plasmacytoid Urothelial Carcinoma.

Context.—: Metastatic pleomorphic lobular carcinoma (MPLC) to the bladder is rare and has considerable histologic and immunohistochemical overlap with plasmacytoid urothelial carcinoma (PUC).

Objective.—: To distinguish MPLC from PUC morphologically and immunohistochemically, including a newer marker, TRPS1.

Design.—: Ten MPLCs to the bladder were reassessed and stained with estrogen, progesterone, and androgen receptors; GATA3; keratin 5/6; HMWK; GCDFP-15; and TRPS1. Sixteen PUCs constituted controls.

Results.—: We studied 4 transurethral resections of bladder tumors and 6 biopsies from 10 women (median age, 69 years) who had breast cancer on average 15 years prior. Microscopic patterns included single cells and cords of cells (n = 4), nests/sheets of dyscohesive cells (n = 2), or both (n = 4). All tumors had cells with voluminous eosinophilic cytoplasm and eccentric nuclei mimicking PUC, and 7 of 10 tumors had signet ring cells. MPLCs were positive for estrogen (8 of 10), progesterone (3 of 7), and androgen (4 of 10) receptors; GCDFP-15 (7 of 10); GATA3 (9 of 10); HMWK (7 of 8); and TRPS1 (7 of 10). No MPLCs stained for keratin 5/6 (n = 9). Of 16 PUCs, 2 showed faint and 2 demonstrated strong TRSP1 staining; 7 of 16 were negative for p63.

Conclusions.—: MPLC to bladder often presents in patients with a remote history of breast cancer, exhibiting significant histologic and immunohistochemical overlap with PUC. Based on prior works and the current study, estrogen receptor (particularly SP-1), mammaglobin, and p63 help differentiate MPLC from PUC. Keratin 5/6 may aid in distinguishing a less frequent basal-type PUC because it is typically negative in MPLC. Some PUCs express TRPS1. Caution should be exercised because immunophenotypes of these tumors greatly overlap, and ramifications of misclassification are major.

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