成人无镰状细胞特征的VCL-ALK肾细胞癌

Q4 Medicine
Ankur R. Sangoi , Simon Y. Kimm , Emily Chan
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引用次数: 1

摘要

间变性淋巴瘤激酶重排相关肾细胞癌(ALK-RCC)是一种暂时性的肾细胞癌亚型,有越来越多的已发表的融合伴侣。VCL-ALK基因融合是一种罕见的融合伴侣(仅报道了6例),几乎总是与镰状细胞特征相关,通常发生在儿科人群中。在此,我们报告了第二例VCL-ALK基因融合的ALK-RCC,来自一名31岁的女性,没有相关的镰状细胞特征,也是第三例报道的发生在成年患者中的病例。肿瘤(直径8.5 cm,局限于肾脏)主要表现为实体生长,核多形性,细胞质呈横纹肌样或液泡状,PAX8和ALK染色均表现为弥漫性强免疫反应性。基因面板测序证实肿瘤中存在VCL-ALK基因融合。本研究扩展了对这种罕见肿瘤进行潜在靶向药物治疗的临床诊断框架。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
VCL-ALK renal cell carcinoma in adult patient without sickle cell trait

Anaplastic lymphoma kinase rearrangement-associated renal cell carcinoma (ALK-RCC) is a provisional renal cell carcinoma subtype with a growing list of published fusion partners. VCL-ALK gene fusion represents an uncommon fusion partner (only 6 reported cases), almost always associated with sickle cell trait and typically in a pediatric population. Herein, we report only the second case of VCL-ALK gene fusion ALK-RCC from a 31-year-old female without associated sickle cell trait, and also only the third reported case occurring in an adult patient. The tumor (measuring 8.5 cm and confined to the kidney) demonstrated mostly solid growth, pleomorphic nuclei, variably rhabdoid to vacuolated cytoplasm, and showed diffuse strong immunoreactivity for both PAX8 and ALK stains. Gene panel sequencing confirmed VCL-ALK gene fusion in the tumor. This study expands the clinical framework for diagnostic consideration of this rare tumor with potential targeted pharmacotherapy.

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来源期刊
Human Pathology: Case Reports
Human Pathology: Case Reports Medicine-Pathology and Forensic Medicine
CiteScore
0.50
自引率
0.00%
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0
审稿时长
16 weeks
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