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Acute renal failure and severe rhabdomyolysis in a patient with resistant thrombotic thrombocytopenic purpura

机译:耐药性血栓性血小板减少性紫癜患者的急性肾衰竭和严重横纹肌溶解

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摘要

Thrombotic thrombocytopenic purpura (TTP) is a rare, life-threatening disorder. This paper describes the case of a 39-year-old Sudanese male who presented to the emergency room with fever, jaundice, decreased level of consciousness, and worsening kidney function for 7 days, a high lactate dehydrogenase level (1947), severe thrombocytopenia (platelets 8), and numerous schistocytes in the peripheral blood smear. The patient was admitted with a diagnosis of TTP for plasma exchange. Fourteen days later, his creatinine kinase (CK) level rose to >50,000 IU; rhabdomyolysis was suggested. Continuous venovenous hemodialysis (CVVHD) was started. The patient’s CK level remained high, despite CVVHD, until the 6th day, after which this parameter gradually started to decrease. This report highlights a resistant case of TTP that presented with concomitant severe rhabdomyolysis, which demanded aggressive, continuous intervention.
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。本文描述了一名39岁的苏丹男性患者,他在急诊室出现发烧,黄疸,意识下降,肾功能恶化7天,乳酸脱氢酶水平高(1947年),严重血小板减少(血小板8),以及外周血涂片中大量的血细胞。该患者被诊断患有血浆置换的TTP。 14天后,他的肌酸酐激酶(CK)水平升至50,000 IU以上;建议横纹肌溶解。开始进行连续静脉血液透析(CVVHD)。尽管有CVVHD,患者的CK水平仍然很高,直到第6天,此参数逐渐开始下降。该报告重点介绍了TTP耐药病例,并伴有严重横纹肌溶解症,需要积极,持续的干预。

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