同一甲状腺结节同时出现 BRAF V600E 和 NRAS Q61R 突变:病例报告。

IF 0.7 Q3 MEDICINE, GENERAL & INTERNAL AME Case Reports Pub Date : 2024-07-01 eCollection Date: 2024-01-01 DOI:10.21037/acr-23-83
Marianna Brogna, Francesca Collina, Simona Losito, Eduardo Clery, Angela Montone, Michele DelSesto, Gerardo Ferrara
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引用次数: 0

摘要

背景:甲状腺乳头状癌(PTC甲状腺乳头状癌(PTC)是最常见的分化良好的内分泌恶性肿瘤。一般来说,甲状腺结节伴有多种致癌突变的情况并不常见,这种情况的发生可能与肿瘤更具侵袭性的生物学行为有关。RET/PTC重排、RAS和BRAF突变在PTC中被认为是相互排斥的。尽管这些突变对肿瘤生长和生存的影响尚存在争议,但同时存在RET/PTC、RAS或BRAF突变的情况已有记录:我们在此介绍一例罕见病例,患者女性,46 岁,颈部肿块,甲状腺结节经细胞学检查归类为 TIR5。我们在同一叶(右叶)的不同区域发现了当代BRAF p.(Val600Glu) [p.(V600E); c.1799T>A]和NRAS p.(Gln61Arg) [p.(Q61R); c.182A>G]突变;两个病灶表现出不同的形态。突变的 BRAF 病变显示出与典型乳头状癌相符的形态特征。突变的NRAS病变显示出与滤泡变异型乳头状癌相符的形态特征。据我们所知,这是首次同时发现这种通常相互排斥的突变:结论:发现同步突变是一种罕见现象,这表明即使在 PTC 中也存在瘤内异质性(ITH)。有多个突变的患者临床预后较差,通常表现为侵袭性甲状腺癌,这可能会影响手术治疗、化疗和BRAF V600E突变靶向治疗。
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Concomitant BRAF V600E and NRAS Q61R mutations in the same thyroid nodule: a case report.

Background: Papillary thyroid cancer (PTC) is the most common type of well-differentiated endocrine malignancy. Generally, thyroid nodules with multiple oncogenic mutations are uncommon with an occurrence which may be related to more aggressive biological behavior of tumors. RET/PTC rearrangement, RAS, and BRAF mutations are considered to be mutually exclusive in PTC. Concomitant RET/PTC, RAS, or BRAF mutations have been documented, although the impact of these mutations for tumor growth and survival is debated.

Case description: Here we present a rare case of woman 46 years old with a neck mass and thyroid nodule classified as TIR5 on cytological examination. We found contemporary BRAF p.(Val600Glu) [p.(V600E); c.1799T>A] and NRAS p.(Gln61Arg) [p.(Q61R); c.182A>G] mutations in morphologically different areas within the same lobe (the right one); The two lesions show different morphology. The mutated BRAF lesion showed morphological characteristics compatible with classic papillary carcinoma. The mutant NRAS lesion shows morphological features compatible with follicular variant papillary carcinoma. To the best of our knowledges, this is the first time that such mutations, which are normally mutually exclusive, have been detected at the same time.

Conclusions: The finding of synchronous mutations is a rare occurrence suggesting for intratumoral heterogeneity (ITH) even in PTC. Patients with multiple mutations have a clinical worse prognosis, generally characterized by an aggressive thyroid cancer, which may influence the surgical treatment, chemotherapy, and BRAF V600E mutation-targeting therapy.

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