Atypical hemolytic-uremic syndrome (aHUS)

Abstract Atypical hemolytic-uremic syndrome (aHUS) is a diagnosis of exclusion which should be proposed in cases where there is microangiopathic hemolytic anemia, thrombocytopenia and acute kidney injury. It is associated with mutations which cause dysregulation of the complement system and implies...

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Veröffentlicht in:AMC. Acta médica Colombiana 2019-12, Vol.44 (4), p.42-44
Hauptverfasser: Domínguez-Ramírez, Gustavo Adolfo, Blanco-Pertuz, Paola María, Herrera-Rueda, Guillermo Andrés
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Sprache:por
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Zusammenfassung:Abstract Atypical hemolytic-uremic syndrome (aHUS) is a diagnosis of exclusion which should be proposed in cases where there is microangiopathic hemolytic anemia, thrombocytopenia and acute kidney injury. It is associated with mutations which cause dysregulation of the complement system and implies an adverse prognosis and a high risk of progression to chronic kidney disease. Following, we present the case of a patient with aHUS, highlighting the effect and importance of biologic therapy with the monoclonal antibody eculizumab. (Acta Med Colomb 2019; 44. DOI:https://doi.org/10.36104/amc.2019.1301).
ISSN:0120-2448
DOI:10.36104/amc.2019.1301