Uno M, Yamada S, Ozeki S, Okano M, Deguchi T, Kuriyama M, Ban Y, Kawada Y, Okumura N, Tanaka T
Department of Urology, Gifu University School of Medicine.
Nihon Hinyokika Gakkai Zasshi. 1993 Jun;84(6):1130-3. doi: 10.5980/jpnjurol1989.84.1130.
We reported a case of juxtaglomerular cell tumor, which excessively produced renin, resulting in secondary hypertension. A 25-year-old woman complained of headache and nausea. Hypertension and elevation of plasma renin activity were found by physical and laboratory examination. US and CT showed a space occupying lesion at upper pole of the right kidney. Angiography showed a hypovascular area at the corresponding area of the right kidney. Renin-secreting renal tumor of the right kidney was diagnosed and right nephrectomy was performed. Postoperatively, blood pressure and plasma renin activity became normalized and symptoms ameliorated. The juxtaglomerular cell tumor was pathologically confirmed and localization renin in the tumor cells was shown by immunohistochemical study. Forty one cases of juxtaglomerular cell tumor have been reported, since Robertson reported the first case. We discussed the clinical and pathological characteristics of the disease in this report.
我们报告了一例近球细胞肿瘤,该肿瘤过度分泌肾素,导致继发性高血压。一名25岁女性主诉头痛和恶心。体格检查和实验室检查发现高血压和血浆肾素活性升高。超声和CT显示右肾上极有占位性病变。血管造影显示右肾相应区域有血管减少区。诊断为右肾分泌肾素的肿瘤,并进行了右肾切除术。术后,血压和血浆肾素活性恢复正常,症状改善。病理证实为近球细胞肿瘤,免疫组化研究显示肿瘤细胞中有定位肾素。自罗伯逊报告首例近球细胞肿瘤以来,已报告了41例。我们在本报告中讨论了该疾病的临床和病理特征。