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[一例从难治性附睾炎病理结果诊断出的结节性多动脉炎病例]

[A Case of Polyarteritis Nodosa Diagnosed from Pathological Findings of Refractory Epididymitis].

作者信息

Horii Sayaka, Iwanishi Toshichika, Kishimoto Nozomu, Kobayashi Masao, Ono Yutaka

机构信息

The Department of Urology, Higashiosaka City Medical Center.

出版信息

Hinyokika Kiyo. 2018 Dec;64(12):515-518. doi: 10.14989/ActaUrolJap_64_12_515.

Abstract

A 54-year-old man was admitted to internal medicine due to unidentified fever persisting for 3 months, and was examined. Then, he was referred to our department for suspected pyelonephritis. Although he was initially being treated for pyelonephritis, right epididymitis occurred during the course of treatment. Antibiotics were ineffective, and symptoms such as weakness and subctaneous nodules also appeared. We performed epididymectomy to differentiate this intractable epididymitis from other systemic diseases. Pathological findings were fibrinoid necrotic vasculitis of middle and small arteries. Of the diagnostic criteria for polyarteritis nodosa, 4 major symptoms and histological findings were satisfied. After we started oral administration of predonin, the fever went down and the creative protein level decreased immediatately.

摘要

一名54岁男性因不明原因发热持续3个月入住内科并接受检查。随后,因怀疑肾盂肾炎被转诊至我科。尽管最初按肾盂肾炎进行治疗,但在治疗过程中出现了右侧附睾炎。抗生素治疗无效,还出现了乏力和皮下结节等症状。为了将这种难治性附睾炎与其他全身性疾病相鉴别,我们进行了附睾切除术。病理结果显示为中小动脉的纤维蛋白样坏死性血管炎。结节性多动脉炎的诊断标准中,4项主要症状及组织学表现均符合。开始口服泼尼松后,发热消退,C反应蛋白水平立即下降。

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