【显微镜下多血管炎合并非特异性间质性肺炎1例】。

Ryumachi. [Rheumatism] Pub Date : 2003-10-01
Yukiko Takeda, Akiko Aoki, Takashi Tsuji, Midori Misumi, Haruko Ideguchi, Yuko Inoue, Atsuhisa Ueda, Shigeru Ohno, Mitsuhiro Takeno, Yoshiaki Ishigatsubo
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引用次数: 0

摘要

非特异性间质性肺炎最初表现为显微镜下多血管炎患者。一名62岁男子于2001年3月因发热和间歇性下肢肌痛入院。自1996年以来,胸部x线片显示双侧中、下肺野网状影。就在入院前,患者在另一家医院通过电视胸腔镜手术(VATS)获得的标本被诊断为非特异性间质性肺炎(NSIP)。入院体检发现双侧锁骨炎。实验室数据显示CRP和KL-6水平升高,多克隆γ球蛋白血症,类风湿因子和髓过氧化物酶抗中性粒细胞胞浆抗体(MPO-ANCA)阳性。感觉和运动神经传导速度在左侧腓神经延迟,而其他神经未见延迟,提示单神经病变。左股四头肌活检标本显示动脉血管炎。除蛋白尿和血尿阳性外,肾脏未见病理损害。从所有这些结果来看,患者被诊断为显微镜下的多血管炎(MPA),没有肾脏受累。甲基强的松龙脉冲治疗后静脉环磷酰胺脉冲治疗改善了患者的临床症状,如发热、咳嗽、肌痛、巩膜炎和呼吸道症状,血清MPO-ANCA滴度降低。此后,强的松龙的剂量成功减少到10mg /天,没有临床复发。在目前以MPA为初始表现的非特异性间质性肺炎患者中,VATS提供了有用的诊断和预后信息,从而导致适当的治疗选择。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[A case of non-specific interstitial pneumonia in patient with microscopic polyangiitis].

Non-specific interstitial pneumonia developed as an initial manifestation in a patient with microscopic polyangiitis. A 62-year-old man was admitted to our hospital in March 2001, because of fever and intermittent myalgia of lower extremities. Chest X-ray had revealed reticular shadows in the bilateral middle and lower lung fields since 1996. Just before admission, the patient had been diagnosed as having nonspecific interstitial pneumonia (NSIP) from the specimen obtained by video-assisted thoracoscopic surgery (VATS) in another hospital. Physical examination on admission revealed bilateral episcleritis. Laboratory data showed elevated levels of CRP and KL-6, polyclonal gammaglobulinemia, positive rheumatoid factor and myeloperoxidase-antineutrophil cytoplasmic antibody (MPO-ANCA). Sensory and motor nerve conducting velocities were delayed in left peroneal nerve, but not other nerves, suggesting mononeuropathy. Biopsied specimens of the left quadriceps revealed vasculitis of arteioles. In spite of positive proteinuria and hematuria, no pathological lesion was found in the kidney. From all of these findings, the patient was diagnosed as having microscopic polyangiitis (MPA) without renal involvement. Methylprednisolone pulse therapy followed by intravenous cyclophosphamide pulse therapy improved his clinical conditions such as pyrexia, cough, myalgia, episcleritis and respiratory symptoms with decreased titer of serum MPO-ANCA. Thereafter, the dose of prednisolone was successfully tapered to 10 mg/day without clinical relapse. In the present patient who developed demonstrated non-specific interstitial pneumonia as an initial manifestation of MPA, VATS provided useful diagnostic and prognostic information, leading to an appropriate therapeutic choice.

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