Abstract
We experienced a favorable outcome in an adult case of atypical hemolytic uremic syndrome (aHUS) after long-term eculizumab treatment. A 38-year-old Japanese man with a history of central retinal vein occlusion was admitted to our hospital with progressive dyspnea. He was found to have non-immune hemolytic anemia, thrombocytopenia, and acute renal failure two weeks after an episode of the common cold. Plasma exchange was ineffective; therefore, we initiated eculizumab after we excluded other thrombotic microangiopathies. Although long-term peritoneal dialysis was required, we successfully discontinued dialysis 18 months after the onset of aHUS with eculizumab.
Original language | English |
---|---|
Pages (from-to) | 1085-1088 |
Number of pages | 4 |
Journal | Internal Medicine |
Volume | 56 |
Issue number | 9 |
DOIs | |
Publication status | Published - 2017 |
Externally published | Yes |
Keywords
- Atypical hemolytic uremic syndrome
- Eculizumab
- Peritoneal dialysis
- Thrombotic microangiopathy
ASJC Scopus subject areas
- Internal Medicine