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Detection and genomic characterization of a mammary-like adenocarcinoma

机译:乳腺样腺癌的检测和基因组表征

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摘要

Whole-genome and transcriptome sequencing were performed to identify potential therapeutic strategies in the absence of viable treatment options for a patient initially diagnosed with vulvar adenocarcinoma. Genomic events were prioritized by comparison against variant distributions in the TCGA pan-cancer data set and complemented with detailed transcriptome sequencing and copy-number analysis. These findings were considered against published scientific literature in order to evaluate the functional effects of potentially relevant genomic events. Analysis of the transcriptome against a background of 27 TCGA cancer types led to reclassification of the tumor as a primary HER2+ mammary-like adenocarcinoma of the vulva. This revised diagnosis was subsequently confirmed by follow-up immunohistochemistry for a mammary-like adenocarcinoma. The patient was treated with chemotherapy and targeted therapies for HER2+ breast cancer. The detailed pathology and genomic findings of this case are presented herein.
机译:在没有可行的治疗选择的情况下,对最初诊断为外阴腺癌的患者进行了全基因组和转录组测序,以确定潜在的治疗策略。通过与TCGA泛癌数据集中的变体分布进行比较来确定基因组事件的优先级,并辅以详细的转录组测序和拷贝数分析。为了评估潜在相关基因组事件的功能影响,将这些发现与已发表的科学文献进行了比较。在27种TCGA癌症类型的背景下对转录组进行分析导致该肿瘤被重新分类为原发性外阴性HER2 + 乳腺样腺癌。随后,通过对乳腺样腺癌的后续免疫组织化学证实了这一修订的诊断。该患者接受了针对HER2 + 乳腺癌的化疗和靶向治疗。本文介绍了这种情况的详细病理学和基因组发现。

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