Aditya Chauhan, Siddhartha Sen, Khalid Amin, Lynn A Burmeister
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引用次数: 0
摘要
在甲状腺乳头状癌(PTC)中,多个驱动突变的频率和影响尚未被广泛探讨,其中驱动突变最常见的是孤立的。我们提出一个62岁的女性病例,她被发现有一个2.6厘米的经典,非侵袭性PTC。下一代测序小组评估肿瘤的突变。我们发现了5个独特的单核苷酸序列变异:BRAF D594N、NRAS Q61H、PIK3CA G1007R、PTEN R335*和PTEN Y225*,这些变异均未在The Cancer Genome Atlas研究中发现。我们认为5个致病变异是迄今为止报道的原发性PTC切除标本的最高数量。观察到的典型PTC行为可能是由于单个致病变异驱动致癌过程的强度较弱。在这种情况下,大量的基因改变并没有转化为侵袭性的组织病理学或临床病程。
Papillary Thyroid Carcinoma With 5 Unique Point Mutations and Typical Behavior.
The frequency and impact of multiple driver mutations have not been extensively explored in papillary thyroid carcinoma (PTC), in which driver mutations are most commonly solitary. We present a case of a 62-year-old female who was found to have a 2.6-cm classical, nonaggressive-appearing PTC. A next-generation sequencing panel assessed the tumor for mutations. Five unique single nucleotide sequence variants, none of which was seen in The Cancer Genome Atlas study on PTC, were found: BRAF D594N, NRAS Q61H, PIK3CA G1007R, PTEN R335*, and PTEN Y225*. We believe that 5 pathogenic variants are the highest reported number for a primary PTC resection specimen to date. The observed typical PTC behavior may be due to a weaker strength of the individual pathogenic variants to drive oncogenic processes. In this case, the high number of genetic alterations did not translate into aggressive histopathology or clinical course.