Hemolytic kidney failure and transient ischemic attack in a 32-year-old female

被引:0
|
作者
Anders, R. [1 ]
Grohmann, M. [2 ]
Lindner, T. H. [1 ]
Bergmann, C. [2 ]
Halbritter, J. [1 ]
机构
[1] Univ Klinikum Leipzig, Klin Endokrinol Nephrol, Dept Innere Med Neurol & Dermatol, Liebigstr 20, D-04103 Leipzig, Germany
[2] Bioscientia, Zentrum Humangenet, Ingelheim, Germany
来源
INTERNIST | 2016年 / 57卷 / 10期
关键词
Kidney failure; Atypical hemolytic uremic syndrome; Thrombotic microangiopathy; Eculizumab; Complement pathway; UREMIC SYNDROME; MUTATIONS; PREDISPOSE; MCP;
D O I
10.1007/s00108-016-0092-0
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
We report on the case of a 32-year-old female patient who initially presented with oliguric acute renal failure, hemolytic anemia with moderate thrombocytopenia and subsequently developed a transient ischemic attack in the cerebellum. The kidney biopsy revealed clinically suspected atypical hemolytic-uremic syndrome (aHUS), which was confirmed by intraglomerular thrombotic microangiopathy (TMA). Treatment with plasmapheresis and sustained administration of the C5 inhibitor eculizumab resulted in hematological remission but without improvement of kidney function. Further etiological investigations led to reduced plasma levels of inhibitory complement factor I on the basis of a heterozygous CFI mutation. In patients with aHUS molecular genetic investigations are indicated in order to determine the underlying cause, to regulate the therapeutic regimen and to allow prognostic statements with respect to a potential kidney transplantation.
引用
收藏
页码:1022 / 1028
页数:7
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