肌上皮癌前多形性腺瘤暴露RET种系突变:罕见的遗传事件。

IF 4.1
Manar Al Masri, Phillip Pirgousis, Alok A Bhatt, Jordan Reynolds, Douglas Riegert-Johnson, Shweta Agarwal
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引用次数: 0

摘要

肌上皮癌(Myoepithelial carcinoma, MECA)是一种完全由肌上皮细胞组成的恶性肿瘤,占所有唾液腺肿瘤的不到1%。由于与良性病变的组织学重叠以及其多变的形态表现,其诊断往往具有挑战性。虽然分子谱分析已成为唾液腺肿瘤分类的一种有价值的工具,但MECA的遗传格局仍然不完全确定。我们报告一例65岁男性慢性淋巴细胞白血病病史,表现为耳痛、喉咙痛和吞咽困难,最终被诊断为颌下腺高度MECA。术前影像学显示广泛的区域性淋巴结病变,并可能转移到肺部和肋骨,下一代测序(NGS)发现了RET p.V804M变异,众所周知,该变异在甲状腺髓样癌中具有致病性,但此前未在MECA中报道。在随后发现这种遗传变化是种系的之后,这一发现扩大了RET作为肿瘤驱动因素的广度,特别是考虑到患者出现时年龄较大,唾液腺肿瘤的RET改变最常与遗传融合事件相关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Myoepithelial Carcinoma Ex-Pleomorphic Adenoma Exposing a RET Germline Mutation: A Rare Genetic Event.

Myoepithelial carcinoma (MECA) is a malignant neoplasm composed exclusively of myoepithelial cells and accounts for less than 1% of all salivary gland tumors. Its diagnosis is often challenging due to histologic overlaps with benign lesions and its variable morphologic presentation. Although molecular profiling has emerged as a valuable tool in salivary gland tumor classification, the genetic landscape of MECA remains incompletely defined. We report a case of a 65-year-old male with a history of chronic lymphocytic leukemia who presented with otalgia, sore throat, and dysphagia, ultimately diagnosed with a high-grade MECA of the submandibular gland following excision. Preoperative imaging revealed extensive regional lymphadenopathy and likely metastases to the lungs and ribs, and next-generation sequencing (NGS) identified a RET p.V804M variant, well-known to be pathogenic in medullary thyroid carcinoma but previously unreported in MECA. After this genetic change was subsequently found to be germline, this finding expands the implications for the breadth of RET as a tumor driver, particularly given the patient's older age at presentation, with RET alterations in salivary tumors most commonly associated with genetic fusion events.

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