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孤立性肾结节病所致的肉芽肿性间质性肾炎。

Granulomatous interstitial nephritis due to isolated renal sarcoidosis.

作者信息

Miyoshi Ken-ichi, Okura Takafumi, Manabe Seiko, Watanabe Sanae, Fukuoka Tomikazu, Higaki Jitsuo

机构信息

Second Department of Internal Medicine, Ehime University School of Medicine, Shitsukawa, Shigenobu-cho, Onsen-gun, Ehime 791-0295, Japan.

出版信息

Clin Exp Nephrol. 2004 Sep;8(3):279-82. doi: 10.1007/s10157-004-0294-y.

Abstract

An 81-year-old woman was admitted to our hospital because of acute exacerbation of chronic renal failure. Her 24-h urine protein value was 0.37 g, but neither hematuria nor leukocyturia was seen. Renal biopsy specimens showed noncaseating granulomas with giant cells in the interstitium. A clinical examination revealed no evidence of tuberculosis, fungus, or malignancy. All of the drugs she had been taking were discontinued, but her renal function continued to deteriorate. No uveitis, erythema nodosum, or common macular skin lesion was seen. A computed tomography scan of the thorax and a total-body gallium-67 scan showed no abnormalities. The serum lysozyme level was greater than four times above normal. Finally, a diagnosis was made, of granulomatous interstitial nephritis due to isolated renal sarcoidosis. Treatment was started with 60 mg/day of prednisolone, and she had an excellent response. Her serum creatinine level decreased to the level shown before the acute exacerbation. It is important to consider renal sarcoidosis as a differential diagnosis in patients with severely progressive renal failure, because corticosteroid therapy is very effective.

摘要

一名81岁女性因慢性肾衰竭急性加重入住我院。她的24小时尿蛋白值为0.37克,但未发现血尿和白细胞尿。肾活检标本显示间质中有非干酪样肉芽肿伴巨细胞。临床检查未发现结核病、真菌或恶性肿瘤的证据。她之前服用的所有药物均已停用,但她的肾功能仍继续恶化。未发现葡萄膜炎、结节性红斑或常见的黄斑皮肤病变。胸部计算机断层扫描和全身镓-67扫描均未发现异常。血清溶菌酶水平高于正常四倍以上。最终,诊断为孤立性肾结节病所致的肉芽肿性间质性肾炎。开始使用泼尼松龙60毫克/天进行治疗,她对此反应良好。她的血清肌酐水平降至急性加重前所示水平。对于严重进行性肾衰竭患者,将肾结节病作为鉴别诊断很重要,因为皮质类固醇治疗非常有效。

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