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Double relapse of incomplete form of thrombotic thrombocytopenic purpura.

机译:血栓性血小板减少性紫癜的不完全形式两次复发。

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BACKGROUND: Although several etiologies can be identified in thrombotic thrompocytopenic purpura (TTP), idiopathic cases are still frequent. Incomplete forms are rare and the diagnosis should be suspected in case of thrombocytopenia and microangiopathic haemolytic anaemia. Relapses are frequent in the complete classic form but rarely reported in incomplete forms. According to the literature, mortality and morbidity are significantly improved with plasma exchange (PE). Nevertheless, the management and treatment of relapses remain problematic.CASE REPORT: A 35-year-old woman presented with a double relapse of an incomplete TTP form in the second (24 months) and the fourth year (40 months) after the initial episode. The patient underwent plasma infusion, PE, and was then started on corticosteroids. She also received antiplatelet agents. The main biological indicators were platelet count, haematocrit, lactate dehydrogenase level and schistocytes. Following this treatment, the patient's condition rapidly improved.CONCLUSION: In this incomplete form of TTP, two relapses occured, with the same presentation. Standard therapy was effective in this case.
机译:背景:尽管在血栓性血小板减少性紫癜(TTP)中可以发现几种病因,但特发性病例仍然很常见。形式不完整的情况很少见,如果发生血小板减少症和微血管性溶血性贫血,应怀疑诊断。复发以完全经典形式频繁发生,但很少以不完全形式报道。根据文献,血浆置换(PE)可显着改善死亡率和发病率。然而,复发的管理和治疗仍然存在问题。病例报告:一名35岁女性在初次发作后的第二个(24个月)和第四年(40个月)出现不完全TTP形式的双重复发。 。患者接受血浆输注PE,然后开始使用糖皮质激素治疗。她还接受了抗血小板药。主要生物学指标为血小板计数,血细胞比容,乳酸脱氢酶水平和血细胞。结论:在这种不完全的TTP形式下,出现了两次复发,表现相同。在这种情况下,标准疗法是有效的。

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