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首页> 外文期刊>Medicine. >Henoch-Sch?nlein Purpura in Northern Spain: Clinical Spectrum of the Disease in 417 Patients From a Single Center
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Henoch-Sch?nlein Purpura in Northern Spain: Clinical Spectrum of the Disease in 417 Patients From a Single Center

机译:西班牙北部Henoch-Sch?nlein紫癜:来自单一中心的417例患者的临床疾病谱

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Abstract: The severity of clinical features and the outcomes in previous series of patients reported with Henoch-Sch?nlein purpura (HSP) vary greatly, probably due to selection bias. To establish the actual clinical spectrum of HSP in all age groups using an unselected and wide series of patients diagnosed at a single center, we performed a retrospective review of 417 patients classified as having HSP according to the criteria proposed by Michel et al. Of 417 patients, 240 were male and 177 female, with a median age at the time of disease diagnosis of 7.5 years (interquartile range [IQR], 5.3–20.1 yr). Three-quarters of the patients were children or young people aged 20 years or younger (n = 315), and one-quarter were adults (n = 102). The most frequent precipitating events were a previous infection (38%), usually an upper respiratory tract infection, and/or drug intake (18.5%) shortly before the onset of the vasculitis. At disease onset the most common manifestations were skin lesions (55.9%), nephropathy (24%), gastrointestinal involvement (13.7%), joint symptoms (9.1%), and fever (6.2%). Cutaneous involvement occurring in all patients, mainly purpuric skin lesion, was the most common manifestation when the vasculitis was fully established, followed by gastrointestinal (64.5%), joint (63.1%), and renal involvement (41.2%). The main laboratory findings were leukocytosis (36.7%), anemia (8.9%), and increased serum IgA levels (31.7%). The most frequent therapies used were corticosteroids (35%), nonsteroidal antiinflammatory drugs (14%), and cytotoxic agents (5%). After a median follow-up of 12 months (IQR, 2–38 mo), complete recovery was observed in most cases (n = 346; 83.2%), while persistent, usually mild, nephropathy was observed in only 32 (7.7%) cases. Relapses were observed in almost a third of patients (n = 133; 31.9%). In conclusion, although HSP is a typical vasculitis affecting children and young people, it is not uncommon in adults. The prognosis is favorable in most cases, depending largely on renal involvement.
机译:摘要:过敏性紫癜(Henoch-Sch?nlein purpura,HSP)报告的先前系列患者的临床特征和预后严重程度差异很大,可能是由于选择偏倚。为了使用在一个中心诊断的未经选择且广泛的一系列患者来确定所有年龄组中HSP的实际临床谱,我们根据Michel等人提出的标准对417例归类为HSP的患者进行了回顾性研究。在417例患者中,男性240例,女性177例,疾病诊断时的中位年龄为7.5岁(四分位间距[IQR],5.3-20.1岁)。四分之三的患者是年龄在20岁以下的儿童或年轻人(n = 315),四分之一是成年人(n = 102)。最频繁的沉淀事件是血管炎发作前不久的先前感染(38%),通常是上呼吸道感染和/或药物摄入(18.5%)。发病时最常见的表现是皮肤病变(55.9%),肾病(24%),胃肠道受累(13.7%),关节症状(9.1%)和发烧(6.2%)。血管炎完全建立后,所有患者的皮肤受累最主要是紫癜性皮肤病变,其次是胃肠道受累(64.5%),关节受累(63.1%)和肾脏受累(41.2%)。实验室的主要发现是白细胞增多(36.7%),贫血(8.9%)和血清IgA水平升高(31.7%)。使用最频繁的疗法是皮质类固醇(35%),非甾体类抗炎药(14%)和细胞毒剂(5%)。在中位随访12个月(IQR,2-38个月)后,大多数情况下观察到完全康复(n = 346; 83.2%),而只有32例(7.7%)观察到持续的,通常为轻度的肾病。案件。在几乎三分之一的患者中观察到复发(n = 133; 31.9%)。总之,尽管HSP是影响儿童和年轻人的典型血管炎,但在成年人中并不少见。在大多数情况下,预后良好,这在很大程度上取决于肾脏受累情况。

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