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Atypical haemolytic uremic syndrome from multiple missenses to a full-blown disease

Filipe Santos Mira1,2, Ana Luísa Nunes3, Ana Rita Elvas3

  • 1Nephrology, Centro Hospitalar e Universitario de Coimbra EPE, Coimbra, Portugal.

BMJ Case Reports
|June 30, 2019
PubMed

A 72-year-old woman was admitted to the hospital because of dorsal, lumbar and lower abdomen pain that had started 4 days before. She had a history of age-related macular degeneration (treated with intraocular bevacizumab). Blood tests showed anaemia, thrombocytopaenia, acute kidney injury, elevated liver enzymes and total bilirubin (mainly because of the indirect fraction). Viral serologies and ADAMTS13 activity levels were normal, and stool testing was negative for Escherichia coli-producing Shiga toxins. E. coli was isolated in urine. Atypical haemolytic uremic syndrome triggered by a urinary tract infection or by the vascular endothelial growth factor-inhibitor bevacizumab were the most likely hypothesis. The patient started urgent plasmapheresis and dialysis that lasted for a total of 18 days. There was complete remission and recovery of kidney function allowing for treatment discontinuation, and she was discharged home. After 6 months of follow-up, she shows no signs of relapse.

Keywords:
acute renal failuredialysisfluid electrolyte and acid-base disturbanceshaematology (incl blood transfusion)

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