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罕见病例报告:乳腺型原发性外阴腺癌
Received 31 October 2024
Accepted for publication 2 February 2025
Published 12 February 2025 Volume 2025:17 Pages 399—405
DOI https://doi.org/10.2147/IJWH.S503901
Checked for plagiarism Yes
Review by Single anonymous peer review
Peer reviewer comments 2
Editor who approved publication: Dr Vinay Kumar
Xiaomin Dai, Huan Lei, Ruixia Jie
Department of Pathology, Zhejiang Hospital, Hangzhou, Zhejiang, People’s Republic of China
Correspondence: Ruixia Jie, Email 632331879@qq.com
Abstract: Primary vulvar adenocarcinoma of mammary gland type (AMGT) is exceedingly rare and presents significant diagnostic challenges. We report the case of a 70-year-old female with a nodular vulvar lesion, confirmed as vulvar AMGT through comprehensive histological and immunohistochemical analysis. The tumor cells were positive for SOX10, TRPS1, and E-cadherin, and negative for ER, PR, and HER-2/neu, ruling out metastatic breast carcinoma. This case underscores the importance of specific markers like TRPS1 in accurately diagnosing rare vulvar malignancies and guiding effective treatment strategies. Further studies are needed to better understand the pathogenesis and clinical characteristics of vulvar AMGT.
Keywords: vulva, adenocarcinoma, mammary gland type, differential diagnosis