Digital papillary adenocarcinoma of the ankle

Avani Singh, Michael Kuncewitch, P. Mansoori, James T. Mothershed, E. Levine
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Abstract

Digital Papillary Adenocarcinoma (DPA) is a very rare neoplasm of sweat glands, with approximately 100 cases in the literature. We present a rare case of DPA of the ankle in a 66-year-old African American man. DPA has a high potential for metastases to the lung and lymph nodes, and initial treatment often entails wide excision or complete digital amputation. DPA typically presents as a painless lesion or mass of the distal digits of the hands or feet. With the limited available literature regarding this malignancy, there is no standard approach to treatment. Wide excisional margins with sentinel lymph node mapping and biopsy are based on extrapolation for other tumors. In the following report, we discuss a representative case and the current literature on the presentation, treatment and pathology of this rare neoplasm.
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足踝指乳头状腺癌
指乳头腺癌(DPA)是一种非常罕见的汗腺肿瘤,文献中约有100例。我们报告了一例罕见的66岁非裔美国男子的脚踝DPA。DPA很有可能转移到肺和淋巴结,最初的治疗通常需要大范围切除或完全截肢。DPA通常表现为手或脚的远端指的无痛病变或肿块。关于这种恶性肿瘤的现有文献有限,目前还没有标准的治疗方法。前哨淋巴结定位和活检的宽切缘是基于对其他肿瘤的推断。在下面的报告中,我们讨论了一个具有代表性的病例和目前关于这种罕见肿瘤的表现、治疗和病理学的文献。
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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