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Rev. esp. anestesiol. reanim ; 69(3)Mar 2022. graf
Article in Spanish | IBECS | ID: ibc-205042

ABSTRACT

Las microangiopatías trombóticas (MAT) son un conjunto de síndromes clínicos que asocian anemia hemolítica, trombocitopenia y disfunción orgánica, principalmente renal o neurológica. Están asociados a una morbimortalidad significativa, por lo que su diagnóstico y tratamiento precoz son esenciales. En este artículo detallamos 2 casos de MAT; una paciente con una púrpura trombocitopénica trombótica (PTT) y otra paciente con un síndrome hemolítico urémico atípico (SHUa).(AU)


Thrombotic microangiopathies (TMA) are a group of clinical syndromes associated with haemolytic anaemia, thrombocytopenia and organ dysfunction, mainly renal or neurological. They are associated with significant morbidity and mortality, so early diagnosis and treatment are essential. In this article we report two cases of TMA; a patient with thrombotic thrombocytopenic purpura (TTP) and a patient with atypical haemolytic uraemic syndrome (aHUS).(AU)


Subject(s)
Humans , Female , Adult , Middle Aged , Thrombotic Microangiopathies/congenital , Thrombotic Microangiopathies/drug therapy , Thrombotic Microangiopathies/therapy , Anemia, Hemolytic , Thrombocytopenia , Atypical Hemolytic Uremic Syndrome , Purpura, Thrombotic Thrombocytopenic , ADAMTS13 Protein , Anesthesiology , Cardiopulmonary Resuscitation , Indicators of Morbidity and Mortality
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