Abstract
Atypical hemolytic uremic syndrome (aHUS) is a life-threatening disease causing systemic thrombotic microangiopathy (TMA) due to the fact of complement dysregulation. Immune activation by viruses, including SARS-CoV-2, can lead to the development of an episode of aHUS against a background of genetic dysregulation in the complement pathway. This paper presents an analysis of two cases of aHUS—siblings diagnosed with familial disease, with a genetic predisposition to aHUS, in whom infection with SARS-CoV-2 was a strong trigger of disease recurrence. The quick recognition and treatment with eculizumab in the early stage of the disease resulted in a rapid improvement in clinical conditions and laboratory parameters.
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Smarz-Widelska, I., Syroka-Główka, M., Janowska-Jaremek, J., Kozioł, M. M., & Załuska, W. (2022). Atypical Hemolytic Uremic Syndrome after SARS-CoV-2 Infection: Report of Two Cases. International Journal of Environmental Research and Public Health, 19(18). https://doi.org/10.3390/ijerph191811437
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