乳腺原发性内分泌性多孔癌1例报告及文献复习。

Pub Date : 2022-01-01 DOI:10.1155/2022/4042298
Yi Xin Li, Mihir Gudi, Zhiyan Yan
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引用次数: 0

摘要

EPC是一种罕见的皮肤肿瘤,自1963年首次报道以来,全球报告病例不足500例。EPC倾向于影响老年人,最常影响头颈部。EPC治疗的主要方法是手术,在淋巴结受累或存在不利特征的情况下进行淋巴结切除术。没有证据可以指导辅助化疗或放疗的使用。由于其多种临床和组织病理学模拟,特别是在不常见的表现部位,如乳房,EPC容易被误诊。在此,我们报告的情况下,59岁的妇女谁提出了一个左乳房皮肤肿块。活检标本显示浸润性癌累及真皮和表皮,免疫组化染色P63和CK5/6阳性,ER、PR和HER2阴性。肿瘤被切除并诊断为非典型特征的EPC,在组织病理学分析中发现鳞状细胞癌(SCC)的重叠特征。在我们的病例中,简单的乳房切除术,宽边缘和腋窝淋巴结清扫,辅助放疗剂量为60 Gy,未能达到局部区域控制,术后4个月淋巴结复发,证明了这种罕见的恶性肿瘤的侵袭性进程。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Primary Eccrine Porocarcinoma of the Breast: A Case Report and Review of Literature.

Primary Eccrine Porocarcinoma of the Breast: A Case Report and Review of Literature.

Primary Eccrine Porocarcinoma of the Breast: A Case Report and Review of Literature.

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Primary Eccrine Porocarcinoma of the Breast: A Case Report and Review of Literature.

Eccrine porocarcinoma (EPC) is a rare cutaneous neoplasm, with less than 500 reported cases worldwide since it was first described in 1963. EPC tends to affect the elderly and most commonly affects the head and neck. The mainstay of EPC treatment is surgery, with lymphadenectomy in the case of nodal involvement or presence of unfavourable characteristics. No evidence exists to guide the use of adjuvant chemotherapy or radiation. EPC is prone to misdiagnosis given its multiple clinical and histopathological mimics, especially in uncommon sites of presentation such as the breast. Herein, we report the case of a 59-year-old woman who presented with a left breast skin lump. The biopsied specimen revealed an infiltrative carcinoma involving the dermis and epidermis with positive IHC staining for P63 and CK5/6 and negative staining for ER, PR, and HER2. The tumour was resected and diagnosed as EPC with atypical features as overlapping characteristics of squamous cell carcinoma (SCC) were detected on histopathological analysis. In our case, a simple mastectomy with broad margins and axillary lymph node dissection with adjuvant radiotherapy to a dose of 60 Gy failed to achieve loco-regional control with nodal recurrence occurring 4 months postsurgery-a testament to the aggressive course of this rare malignancy.

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