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A fatal case of severe gastrointestinal and renal involvement in Henoch–Sch?nlein purpura

机译:严重的胃肠道和肾脏受累致Henoch-Schonlein紫癜的致命病例

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Henoch-Sch?nlein purpura (HSP) is an immune-complex mediated vasculitis affecting small vessels with dominant IgA deposits. It is seen mostly in children, with a self-limiting disease, but can present with more severe clinical features in older patients, such as gastrointestinal (GI) involvement, with a propensity for rapid progression. In this report, we describe our experience with a male HSP patient who presented with pneumonia, palpable purpuric rash, severe GI involvement with hemodynamic compromise and acute kidney injury. Even though we escalated therapy over time given the lack of response with each previous strategy, with corticosteroids and cyclophosphamide, he developed massive lower gastrointestinal hemorrhage that was not responsive to any supportive measure and died as a result of hemorrhagic shock. There was no established protocol that guided this treatment due to lack of rigorous data, which emphasizes the need for more studies on adult HSP in order to establish the optimal management for HSP patients with severe gastrointestinal manifestations.
机译:过敏性紫癜(HSP)是一种免疫复合物介导的血管炎,影响具有主要IgA沉积物的小血管。它主要出现在患有自限性疾病的儿童中,但在老年患者中可能表现出更严重的临床特征,例如胃肠道(GI)受累,并有快速发展的趋势。在本报告中,我们描述了一位男性HSP患者的经历,该患者患有肺炎,可触及的紫癜性皮疹,严重的GI涉及血液动力学损害和急性肾损伤。即使我们由于先前对每种策略缺乏反应(皮质类固醇和环磷酰胺)而逐步提高治疗水平,但他仍发生了巨大的下消化道出血,对任何支持措施均无反应,并因失血性休克而死亡。由于缺乏严格的数据,尚无指导该治疗的既定方案,该方案强调需要对成人HSP进行更多研究,以便为患有严重胃肠道表现的HSP患者建立最佳治疗方法。

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