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由EML4e13-ALKe20融合导致的侵袭性分化型甲状腺癌:病例报告及文献综述

Aggressive Differentiated Thyroid Cancer due to EML4e13-ALKe20 Fusion: A Case Presentation and Review of the Literature.

作者信息

Khthir Rodhan, Shaheen Zainab, Santhanam Prasanna, Sigdel Saroj

机构信息

Marshall University, School of Medicine, Huntington, WV, USA.

Johns Hopkins University, School of Medicine, Baltimore, MD, USA.

出版信息

Case Rep Endocrinol. 2021 Feb 15;2021:8837399. doi: 10.1155/2021/8837399. eCollection 2021.

Abstract

BACKGROUND

Differentiated thyroid cancer (DTC) is an indolent malignancy. It rarely presents with aggressive local invasion and/or distant metastatic disease. . We describe a case of a 30-year-old man with a locally aggressive form of papillary thyroid cancer with fusion (: echinoderm microtubule-associated protein-like 4; : anaplastic lymphoma kinase). He presented with right-side cervical lymphadenopathy with a highly suspicious right-side thyroid nodule. Total thyroidectomy and level IV lymph node resection showed extensive bilateral disease, with extrathyroidal and extranodal extension. FDG-PET CT scan following surgery confirmed the presence of significant residual disease in the neck area. He underwent bilateral lateral lymph node dissection followed by radioactive iodine treatment. Somatic mutation testing showed fusion. . This case represents an aggressive form of DTC with fusion. The rapid progression of clinical signs and symptoms and the local extension beyond the thyroid and lymph nodes with the persistence of high-volume local disease after thyroidectomy highlight the aggressive nature of this mutation and the importance of performing genetic analysis to guide future treatments and determine prognosis.

CONCLUSION

This case highlights the importance of using molecular diagnostics in patient care, especially if the presentation is unusual for DTC. A thorough evaluation of the tumor pathology and the somatic mutational profile analysis are important for obtaining vital therapeutic and prognostic guidance.

摘要

背景

分化型甲状腺癌(DTC)是一种惰性恶性肿瘤。它很少表现为侵袭性局部侵犯和/或远处转移性疾病。我们描述了一例30岁男性,患有局部侵袭性乳头状甲状腺癌,伴有 EML4-ALK 融合(EML4:棘皮动物微管相关蛋白样4;ALK:间变性淋巴瘤激酶)。他表现为右侧颈部淋巴结肿大,右侧甲状腺结节高度可疑。全甲状腺切除术和IV区淋巴结切除术显示双侧广泛病变,伴有甲状腺外和结外扩展。术后的FDG-PET CT扫描证实颈部区域存在大量残留疾病。他接受了双侧侧方淋巴结清扫术,随后进行放射性碘治疗。体细胞突变检测显示EML4-ALK融合。该病例代表了一种伴有EML4-ALK融合的侵袭性DTC形式。临床体征和症状的快速进展以及甲状腺和淋巴结以外的局部扩展,以及甲状腺切除术后大量局部疾病的持续存在,突出了这种突变的侵袭性本质以及进行基因分析以指导未来治疗和确定预后的重要性。

结论

该病例突出了在患者护理中使用分子诊断的重要性,特别是如果临床表现对于DTC来说不寻常。对肿瘤病理学进行全面评估和体细胞突变谱分析对于获得重要的治疗和预后指导很重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/32dd/7899757/ad9bc61f9ef2/CRIE2021-8837399.001.jpg

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