在资源有限的环境中诊断 TFE3 重排肾细胞癌的方法:病例报告。

IF 1.9 Q3 ONCOLOGY
Journal of Kidney Cancer and VHL Pub Date : 2024-08-24 eCollection Date: 2024-01-01 DOI:10.15586/jkcvhl.v11i3.338
Allison Kaye Lombridas Pagarigan, Pamela Delos Reyes-Murillo, Dennis Jose Sienes Carbonell
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引用次数: 0

摘要

本报告叙述了一名女性儿童的诊断过程,她因腹部造影发现巨大肾肿块而出现血尿。对其进行了组织学评估和随后的免疫组化研究。TFE3和α-甲基酰-CoA-racemase的免疫组化表达强烈而明确,碳酸酐酶IX相应呈阴性,加上非常独特的临床、放射学、大体和显微镜检查结果,确诊为TFE3基因重排的肾细胞癌,这在菲律宾尚属首例。在资源匮乏的环境中,评估罕见疾病的分子模式基本不存在,本病例凸显了可靠、可负担和可获得的免疫组化研究的重要作用和重大诊断影响。认识到儿童和青少年肾脏恶性肿瘤的独特形态学、免疫组化和细胞遗传学特征,就能及时对这种侵袭性实体进行治疗干预。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Approach to Diagnosis of TFE3-rearranged Renal Cell Carcinoma in a Limited Resource Setting: A Case Report.

This report recounts the diagnostic workup of a pediatric female who presented with hematuria secondary to a large renal mass visualized on abdominal imaging. Histologic assessment and subsequent immunohistochemistry studies were performed. Intense, unequivocal immunohistochemical expression of TFE3 and alpha-methylacyl-CoA-racemase with corresponding negativity for carbonic anhydrase IX, along with highly distinctive clinical, radiologic, gross, and microscopic findings confirmed the diagnosis of a renal cell carcinoma with TFE3 gene rearrangement - the first ever reported case in the Philippines. This case highlights the vital role and significant diagnostic impact of reliable, affordable and accessible immunohistochemistry studies in low-resource settings where molecular modalities for evaluating rare diseases are largely unavailable. Recognition of distinctive morphologic, immunohistochemical, and cytogenetic features in childhood and adolescent renal malignancies allows for the timely institution of therapeutic interventions for this aggressive entity.

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