Thrombotic Thrombocytopenic Purpura: A Rare Cause of Severe Acute Kidney Injury

被引:1
作者
Najar, Hatem [1 ]
Tuider, Laurene [1 ]
Kukkar, Vinita [2 ]
Quasem, Mohammad [3 ]
机构
[1] United Hlth Serv Hosp, Internal Med Dept, Johnson City, TN 37604 USA
[2] United Hlth Serv Hosp, Pathol Dept, Johnson City, TN USA
[3] United Hlth Serv Hosp, Nephrol Dept, Johnson City, TN USA
关键词
acute kidney injury; therapeutic plasmapheresis; thrombocytopenia; thrombotic thrombocyropenic purpura; thrombotic microangiopathy (tma); MICROANGIOPATHY;
D O I
10.7759/cureus.24221
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Thrombotic microangiopathy (TMA) is a serious and potentially fatal disorder, especially if there is a delay in diagnosis and appropriate treatment. Thrombotic thromhocytopenic purpura (TTP) and hemolytic uremic syndrome (HUS) are the two main forms of TMA. Although severe acute kidney injury (AKI) is a common manifestation of TMA, it remains rarely described in reported TTP cases. We present a rare case of TTP in a 76-year-old African American male who presented with severe AKI (stage 3) and uremic symptoms. Early diagnosis and prompt treatment of TTP with plasmapheresis followed by rituximab and caplacizumab were associated with the resolution of the AKI and avoidance of hemodialysis. This case highlights the need to consider TTP as a possible diagnosis even in the setting of severe AKI.
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页数:4
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