HER2 Negative Mammary Paget's Disease or In Situ Melanoma? A Case Report and Review of the Literature.

IF 0.7 Q4 PATHOLOGY
Luana-Andreea Boșoteanu, Mariana Așchie, Cristian Ionuţ Orǎșanu, Mădălina Boșoteanu
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Abstract

Mammary Paget's disease (MPD) is a rare histological condition, accounting for 1-4% of female breast cancers, which may appear either independently (1.4-13% of the cases), or in association with an in situ or invasive ductal carcinoma (approximately 90% of the cases). The purpose of this article is to highlight the histopathological challenges related to the microscopical polymorphism of this disease and the utmost importance of immunohistochemistry in the thorough process of Paget's disease differential diagnosis. Moreover, the primary objective of this review of literature was to corroborate the existing data concerning the potential peculiar immunohistochemical profile that mammary Paget's disease might express. We report the case of a 44-year-old female patient, histopathologically diagnosed with HER2-negative MPD accompanying an invasive mammary carcinoma. The histopathological and immunohistochemical approach is derived from the exigency of excluding the possibility of synchronous tumors-a mammary invasive carcinoma, accompanied by another component with MPD phenotypic mimicry. The unexpected negative HER2 reaction is conducted to a primary focus on excluding a malignant melanoma in situ. The absence of MelanA and S100 immunoexpression and lack of pigmentation and clinical aspects infirmed it. Bowen's disease was invalidated by its rare presentation in the breast cutaneous tissue and the absence of individual risk factors suggestive of an existing immunosuppressive status. In the case of similar morphoimmunohistochemical aspects, significant expression of Ki-67 signals MPD, an immunoreactivity that helped distinguish the cellular population from Toker cells. The great similarity of MPD with other benign and malignant cutaneous tumors might determine delay or misdiagnosis. Thus, the utmost importance of immunohistochemistry is reflected in its prognostic significance and geared towards extending the therapeutic arsenal.

Abstract Image

Abstract Image

HER2阴性乳腺佩吉特病还是原位黑色素瘤?一例病例报告及文献回顾。
乳腺佩吉特病(MPD)是一种罕见的组织学疾病,占女性乳腺癌的1-4%,其可能单独出现(1.4-13%的病例),也可能与原位或浸润性导管癌相关(约90%的病例)。本文的目的是强调与该疾病的显微多态性相关的组织病理学挑战,以及免疫组织化学在Paget病鉴别诊断的彻底过程中的重要性。此外,本文献综述的主要目的是证实有关乳腺佩吉特病可能表达的潜在特殊免疫组织化学特征的现有数据。我们报告一例44岁的女性患者,组织病理学诊断为her2阴性MPD合并浸润性乳腺癌。组织病理学和免疫组织化学方法源于排除同步肿瘤可能性的迫切需要-乳腺浸润性癌,伴有MPD表型模仿的另一成分。出乎意料的HER2阴性反应主要是为了排除原位恶性黑色素瘤。MelanA和S100免疫表达的缺失以及色素沉着和临床方面的缺乏使其变得虚弱。Bowen病因其在乳腺皮肤组织中的罕见表现和缺乏提示存在免疫抑制状态的个体危险因素而无效。在形态免疫组织化学方面相似的情况下,Ki-67的显著表达表明MPD,这是一种免疫反应性,有助于将细胞群与Toker细胞区分开来。MPD与其他良恶性皮肤肿瘤有很大的相似之处,可能决定其延误或误诊。因此,免疫组织化学的最大重要性反映在其预后意义上,并面向扩大治疗武器库。
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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审稿时长
12 weeks
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