Radiologic and pathologic correlation of a renal venous hemangioma.

IF 0.5 Q4 ONCOLOGY International Cancer Conference Journal Pub Date : 2023-08-04 eCollection Date: 2023-10-01 DOI:10.1007/s13691-023-00626-6
Alperen Elek, Jung Woo Kwon, Sena Ertugrul, Nisa Cem Oren
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Abstract

Renal hemangiomas, including the rare subtype of venous hemangioma, are typically non-cancerous, often asymptomatic, and usually discovered incidentally during imaging studies. Here, we report a unique case of a 59-year-old African-American female with a renal venous hemangioma that initially mimicked papillary-type renal cell carcinoma (RCC-pt) on imaging studies. The patient's presentation included a long history of rectal bleeding and an incidental discovery of a hypoattenuating mass in the left kidney during a contrast-enhanced CT scan. Renal MRI revealed a 3.5 cm left renal lower pole mass, presenting as heterogeneously hyperintense on T1-weighted images and hypointense on T2-weighted images, with gradual mild enhancement post-contrast. Subsequent total nephrectomy confirmed the histopathological diagnosis of a venous hemangioma. This case underlines the need for recognizing unique imaging features of renal venous hemangiomas, contributing to the differential diagnosis of T2 dark hypoenhancing renal masses. Correct interpretation may prevent unnecessary invasive procedures and operations, thereby improving patient management and outcomes.

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肾静脉血管瘤的放射学和病理学相关性。
肾血管瘤,包括罕见的静脉血管瘤亚型,通常是非癌性的,通常无症状,通常在影像学研究中偶然发现。在这里,我们报告了一例独特的病例,一名59岁的非裔美国女性患有肾静脉血管瘤,最初在影像学研究中模仿乳头状肾细胞癌(RCC pt)。患者的表现包括长期直肠出血史,以及在增强CT扫描中偶然发现左肾有一个低衰减肿块。肾MRI显示左肾下极有3.5cm的肿块,在T1加权图像上表现为不均匀高信号,在T2加权图像上呈低信号,对比后逐渐轻度增强。随后的全肾切除术证实了静脉血管瘤的组织病理学诊断。该病例强调了识别肾静脉血管瘤独特影像学特征的必要性,有助于鉴别诊断T2深色低增强肾肿块。正确的解释可以防止不必要的侵入性程序和操作,从而改善患者管理和结果。
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来源期刊
自引率
14.30%
发文量
57
期刊介绍: This online-only journal publishes original case reports on all types of cancer. In particular, we welcome not only case reports of educational value in the diagnosis and treatment of cancers, but also reports on molecularly analyzed cancer cases, including gene mutations, gene fusions, gene expression, and changes in copy number, regardless of their known clinical significance. Assessing the molecular analysis of a tumor usually requires a “cancer conference” in which experts from various fields discuss it. Even if the authors and their respective “cancer conference” were unable to determine the clinical significance of molecular changes at the time of submission and publication, their data may provide evidence that will help the scientific community develop precision medicine solutions in the future. We welcome case reports with reviews of the literature on similar cases, as they are more useful and valuable to readers than are reports of rare cases. International Cancer Conference Journal is the official publication of the Japan Society of Clinical Oncology (JSCO). - Presents an online-only collection of original case reports on all types of cancer - In particular, welcomes molecularly analyzed cancer cases - The Official Publication of the Japan Society of Clinical Oncology (JSCO)
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HER2-targeted therapy is changing. A case of gastritis caused by immune checkpoint inhibitor treated with infliximab. A case of grade1 follicular lymphoma diagnosed by laparoscopic lymph node resection: differentiating from late lymph node recurrence of endometrial cancer. A case report of mucinous borderline ovarian tumor with recurrence as invasive carcinoma with high copy number alterations. SMARCA4-deficient uterine tumors in young women: response to immune checkpoint inhibitors.
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