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Thrombotic microangiopathy in children
(2022-01-01)
The syndrome of thrombotic microangiopathy (TMA) is a clinical-pathological entity characterized by microangiopathic hemolytic anemia, thrombocytopenia, and end organ involvement. It comprises a spectrum of underlying ...
Treatment of thrombotic thrombocytopenic purpura with rituximab. Report of eight cases
(SOC MEDICA SANTIAGO, 2015)
Thrombotic thrombocytopenic purpura, an immune/non-immune thrombotic microangiopathy (TTP/TMA) is associated with high morbidity and mortality, even with appropriate treatment. In patients refractory to standard treatment ...
Histopathological features of thrombotic microangiopathies in renal biopsies
(2019-01-01)
Background: Thrombotic microangiopathy (TMA) is a morphologic lesion characterized by thrombi occluding microvasculature related to endothelial injury. Objectives: This study aimed to assess the association between ...
Complement in secondary thrombotic microangiopathy
Thrombotic microangiopathy (TMA) is a condition characterized by thrombocytopenia and
microangiopathic hemolytic anemia (MAHA) with varying degrees of organ damage in the
setting of normal International Normalized Ratio ...
Acute Cerebrovascular events associated to hemolytic uremic syndrome: Description of two pediatric cases
(2017)
Introduction: Diarrhea-associated Hemolytic Uremic Syndrome (D+HUS) is a multisystem disorder in which neurological involvement (35 to 50%) is associated to adverse outcome. An important cause of a permanent neurological ...
Thrombotic microangiopathy coming of age
(UANL. Facultad de Medicina, 2015)
Thrombotic microangiopathy as first manifestation of acute human immunodeficiency virus infection: a case report and review of the literature
(2016)
Abstract
Background
We present the case of a patient with acute human immunodeficiency virus infection and a thrombotic microangiopathy as the first clinical manifestation, a ...
Critical Appraisal Of Eculizumab For Atypical Hemolytic Uremic Syndrome
(Dove Medical Press LtdAlbany, 2016)
Chronic catastrophic-like antiphospholipid syndrome: a ???smoldering??? variant?
(Springer Verlag, 2009)