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首页> 外文期刊>Reumatologia >Thrombotic thrombocytopenic purpura as the first presentation in systemic lupus erythematosus
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Thrombotic thrombocytopenic purpura as the first presentation in systemic lupus erythematosus

机译:血栓性血小板减少性紫癜首次出现于系统性红斑狼疮

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Thrombotic thrombocytopenic purpura (TTP) is an uncommon, life-threatening disease characterized by severe thrombocytopenia, microangiopathic haemolytic anaemia, neurologic abnormalities, renal insufficiency, and fever commonly associated with infections, malignancy, drugs, and autoimmune diseases. Coexistence of TTP with systemic lupus erythematosus (SLE) is extremely rare, and the emergence of the full manifestation of SLE starting with TTP is even rarer. Black people due to genetic risk factors are at increased risk of TTP. In the present article the authors describe the case of a?Nigerian woman who developed classical features of TTP as the first manifestation of SLE. The patient’s condition was stabilized after treatment with intravenous pulses of methylprednisolone and subsequently on oral prednisolone and hydroxychloroquine treatment.
机译:血栓性血小板减少性紫癜(TTP)是一种罕见的威胁生命的疾病,其特征是严重的血小板减少症,微血管性溶血性贫血,神经系统异常,肾功能不全和发烧,通常与感染,恶性肿瘤,药物和自身免疫性疾病相关。 TTP与系统性红斑狼疮(SLE)并存的情况极为罕见,而且以TTP开头的SLE完整表现的出现更为罕见。由于遗传风险因素,黑人患TTP的风险增加。在本文中,作者描述了一个尼日利亚妇女的案例,该妇女发展了TTP的经典特征,是SLE的第一个表现。静脉注射甲基强的松龙治疗后病情稳定,随后口服泼尼松龙和羟氯喹治疗。

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