[一名6岁女孩的局部肾囊性疾病]。

Q4 Medicine
Kota Fujimoto, Satoko Matsuyama, Futoshi Matsui, Koji Yazawa, Fumi Matsumoto
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引用次数: 0

摘要

局限性肾脏囊性疾病(LCDK)是一种罕见的、非遗传性的、非进行性的良性囊性肾脏疾病。它主要发生在成人中,很少报道发生在儿童中。迄今为止,文献中仅报道了5例青春期前LCDK病例。在这个报告中,我们提出了一个6岁女孩的LCDK与恶性肾肿瘤难以鉴别的病例。不能进行保留肾单位的手术。一名6岁女孩,无既往病史,以肉眼血尿和右侧腹痛表现。当地医院的腹部超声检查显示右肾有多个大小不等的囊肿。她被转介到我们医院作进一步评估。计算机断层扫描显示,囊肿之间的区域在下极的某些部分略有增强,诊断为波斯尼亚分类III。对可能的囊性肾肿瘤行肾切除术。术后通过组织病理学检查诊断为LCDK。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[LOCALIZED CYSTIC DISEASE OF THE KIDNEY IN A 6-YEAR-OLD GIRL].

Localized cystic disease of the kidney (LCDK) is a rare, non-hereditary, non-progressive benign cystic renal condition. It is found primarily in adults, and is rarely reported in children. To date, only 5 prepubertal cases of LCDK have been reported in the literature. In this report, we present a case of LCDK that was difficult to differentiate from malignant renal tumor in a 6-year-old girl. Nephron-sparing surgery could not be performed.A 6-year-old girl with no past medical history presented with gross hematuria and right-sided abdominal pain. An abdominal ultrasound at a local hospital showed multiple variable-sized cysts throughout the right kidney. She was referred to our hospital for further evaluation. Computed tomography demonstrated that the region between cysts was slightly enhanced in some part of the lower pole and was diagnosed III in the Bosniak classification. Nephrectomy was performed for possible cystic renal neoplasm. After surgery, a diagnosis of LCDK was made by histopathological examination.

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来源期刊
Japanese Journal of Urology
Japanese Journal of Urology Medicine-Urology
CiteScore
0.20
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