结节性硬化症患儿肾脏和纵隔血管周围上皮样细胞瘤(PEComas)罕见病例报告。

IF 0.5 Q4 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING BJR Case Reports Pub Date : 2023-03-01 DOI:10.1259/bjrcr.20220105
Kamal H Attia, Ahmad A Al Boukai, Muammar H Mohammed, Maha Arafah
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摘要

我们描述了一个独特的病例血管周围上皮样细胞肿瘤发生纵隔和左肾软组织肿块偶然发现在一个5岁结节性硬化症患者提出上呼吸道疾病的急诊科。影像学特征无特异性。然而,两种病变的相似的CT特征和背景病史引起了对同步间质肿瘤的怀疑,组织病理学证实了诊断。这些肿瘤在儿科人群中罕见,缺乏具体的诊断标准,因此需要报告病例,并强调需要进一步研究此类肿瘤的影像学特征。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Renal and mediastinal perivascular epithelioid cell tumors (PEComas) in a young child with tuberous sclerosis; a rare case report.

We describe a unique case of perivascular epithelioid cell tumors occurring as mediastinal and left renal soft tissue masses discovered incidentally in a 5-year-old tuberous sclerosis patient upon presentation to the emergency department for upper respiratory illness. The radiographic features were non-specific. However, the similar CT characteristics of both lesions and background history raised the suspicion of a synchronous mesenchymal tumor, and histopathology confirmed the diagnosis. The rarity of these tumors in the pediatric population and lack of specific diagnostic criteria impose reporting the case and emphasize the need for further research on imaging features of such tumors.

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BJR Case Reports
BJR Case Reports RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING-
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发文量
77
审稿时长
11 weeks
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