一例与种系EGFR T790M变异体相关的孤立性髓性肉瘤:在体细胞肿瘤测序板上识别潜在种系变异体的重要性

IF 1.3 Q4 HEMATOLOGY
Margaret Walker, Matthew Folstad, Kelcy Smith-Simmer, Erica F Reinig, Kalyan Nadiminti, Lauren Lovrien, J. Churpek, L. Banaszak
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引用次数: 0

摘要

孤立性髓系肉瘤是一种罕见的急性髓系白血病亚型,预后不一。我们报告了一例先前健康的30岁男性,他出现胸痛和体重减轻,发现有一个巨大的纵隔肿块。肿块的活检与孤立的髓系肉瘤一致。体细胞肿瘤测序小组揭示了EGFR T790M变体,该变体后来被证实是种系起源。种系EGFR T790M变异体与癌症遗传易感性相关,尽管髓系恶性肿瘤尚未被描述。据我们所知,这是第一例有潜在种系EGFR T790M突变的骨髓肉瘤病例。随着体细胞肿瘤测序小组变得越来越普遍,重要的是识别潜在的种系变异,以促进适当的遗传咨询转诊,进行验证性基因检测,并为患者及其家人制定个性化的治疗和监测计划。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A Case of Isolated Myeloid Sarcoma Associated With Germline EGFR T790M Variant: The Importance of Recognizing Potential Germline Variants on Somatic Tumor Sequencing Panels
Isolated myeloid sarcoma is an uncommon subtype of acute myeloid leukemia associated with variable prognosis. We present the case of a previously healthy 30-year-old man presenting with chest pain and weight loss who was found to have a large mediastinal mass. Biopsy of the mass was consistent with isolated myeloid sarcoma. A somatic tumor sequencing panel revealed an EGFR T790M variant, which was later confirmed to be of germline origin. Germline EGFR T790M variants are associated with a hereditary predisposition to lung cancer, though myeloid malignancies have not yet been described. To our knowledge, this is the first reported case of myeloid sarcoma in a patient with an underlying germline EGFR T790M mutation. As somatic tumor sequencing panels become more commonplace, it is important to recognize potential germline variants in order to facilitate appropriate referral for genetic counseling, perform confirmatory genetic testing, and to develop a personalized treatment and surveillance plan for patients and their families.
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Journal of hematology
Journal of hematology HEMATOLOGY-
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