病例报告:乳腺型原发性外阴腺癌--通过聚焦新一代测序分析其遗传特征

Lina Hu, James Tiesinga
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摘要

乳腺样外阴腺癌(Mammary-like vulvar adenocarcinoma,MLVA)是一种极为罕见的外阴腺癌亚型,与乳腺组织具有相同的特征。由于其罕见性和缺乏共识,MLVA 给病理学家带来了诊断上的挑战。我们介绍了一例 59 岁女性的病例,她的外生殖器右侧有一个溃疡性肿块,诊断为 MLVA。为了确定肿瘤的特征,我们进行了全面的免疫组化(IHC)和基因测序研究。免疫组化分析显示,肿瘤中激素受体(雌激素受体、孕激素受体和 HER2)三重表达,支持肿瘤来源于乳腺。基因测序发现了与激素标记表达相关的独特基因突变。其中一个融合基因(ERBB2-NAGLU)在任何肿瘤中都未见报道,其他具有独特突变类型的基因突变以前在MLVA中也未见报道。我们的研究结果揭示了MLV的分子特征,可能有助于改善这种罕见类型外阴腺癌的诊断和治疗。
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Case report: Primary vulvar adenocarcinoma of mammary gland type—its genetic characteristics by focused next-generation sequencing
Mammary-like vulvar adenocarcinoma (MLVA) is an exceedingly rare subtype of vulvar adenocarcinoma that shares features with mammary gland tissue. Due to its rarity and lack of consensus, MLVA presents diagnostic challenges to pathologists. We present the case of a 59-year-old female with an ulcerated mass on the right side of the external genitalia, diagnosed as MLVA. Comprehensive immunohistochemistry (IHC) and gene sequencing studies were performed to characterize the tumor. IHC analysis revealed triple expression of hormonal receptors (estrogen receptor, progesterone receptor, and HER2), supporting the mammary gland origin of the tumor. Gene sequencing identified unique genetic mutations associated with the expression of hormonal markers. One fusion gene (ERBB2-NAGLU) has not been reported in any tumors, and other mutations with unique mutation types have not been previously reported in MLVA. Our findings shed light on the molecular characteristics of MLV and may help improve the diagnosis and treatment of this rare type of vulvar adenocarcinoma.
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