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首页> 外文期刊>Clinical rheumatology >Methylprednisolone pulse plus mizoribine in children with Henoch-Schoenlein purpura nephritis.
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Methylprednisolone pulse plus mizoribine in children with Henoch-Schoenlein purpura nephritis.

机译:儿童过敏性紫癜性肾炎患儿甲基强的松龙脉搏加米唑啉碱。

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摘要

We evaluated whether methylprednisolone and urokinase pulse therapy combined with mizoribine (MUPM) was effective in children with severe Henoch-Schoenlein purpura nephritis (HSPN). We studied 12 patients who had been diagnosed with HSPN of at least ISKDC type III. All patients were treated with MUPM. Clinical features, pathological findings, and prognosis were prospectively investigated. Ten patients (responders; nine with ISKDC grade IIIb and one with grade IVb) were treated with MUPM, whereas MUPM was discontinued due to the lack of response in two patients (non-responders; two with grade IVb). Among responders, urinary protein excretion had decreased significantly from 99.7 +/- 37.8 to 25.9 +/- 33.4 mg/m(2) per hour after 3 months of therapy. The acute index and tubulointerstitial scores decreased significantly from 5.8 +/- 1.5 and 3.8 +/- 0.6 at the first biopsy to 2.3 +/- 1.3 and 1.0 +/- 0.8 at the second biopsy, respectively. At the most recent follow-up, eight of the responders had normal urine, and two had minor urinary abnormalities. Non-responders demonstrated continued high levels of urinary protein excretion after 3 months of therapy, and MUPM was discontinued. Our study suggests that MUPM is effective in ameliorating the proteinuria and the histological severity of HSPN in patients with <50% crescents but is not so effective for HSPN in patients with >50% crescents.
机译:我们评估了甲基泼尼松龙和尿激酶脉冲疗法联合米佐利滨(MUPM)在重症过敏性紫癜性紫癜性肾炎(HSPN)儿童中是否有效。我们研究了12例至少被诊断为ISKDC III型HSPN的患者。所有患者均接受MUPM治疗。临床特征,病理结果和预后进行了调查。用MUPM治疗了10例患者(有反应者; ISKDC IIIb级有9名,IVb级有1名),而由于2名患者(无反应者; 2名IVb级)缺乏反应而中断了MUPM。在应答者中,治疗3个月后,每小时尿蛋白排泄量从每小时99.7 +/- 37.8降至25.9 +/- 33.4 mg / m(2)。急性指数和肾小管间质评分分别从第一次活检时的5.8 +/- 1.5和3.8 +/- 0.6显着降低到第二次活检时的2.3 +/- 1.3和1.0 +/- 0.8。在最近的随访中,八名反应者的尿液正常,而两名尿液异常。无反应者在治疗3个月后表现出持续高水平的尿蛋白排泄,并停用了MUPM。我们的研究表明,MUPM可有效改善新月体<50%的患者的蛋白尿和HSPN的组织学严重程度,但不适用于新月体> 50%的患者的HSPN。

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