Results 1 to 10 of about 17,452 (202)
Pulmonary tumor thrombotic microangiopathy presenting as recurrent syncope
Pulmonary tumor thrombotic microangiopathy is a rare condition in which embolization of tumor cells to the pulmonary arterioles causes fibrocellular intimal thickening and activation of the coagulation cascade resulting in pulmonary hypertension and ...
Constanza Burciaga Calderoni +3 more
doaj +1 more source
Association of thrombotic microangiopathy with interferon therapy for hepatitis B: a case report
Background Thrombotic microangiopathy is characterized by microangiopathic hemolytic anemia, thrombocytopenia, and organ injury. The pathological features include vascular damage that is manifested by arteriolar and capillary thrombosis with ...
Shan Wei, Wenjuan Mei, Ying Wang
doaj +1 more source
Background Ocular involvement in catastrophic antiphospholipid syndrome (CAPS), a rare, life-threatening form of antiphospholipid syndrome (APS) that results in multiorgan failure and a high mortality rate, has rarely been reported.
Young In Yun +6 more
doaj +1 more source
Severe Vitamin B12 Deficiency in Pregnancy Mimicking HELLP Syndrome
Severe vitamin B12 deficiency may present with hematologic abnormalities that mimic thrombotic microangiopathy disorders such as hemolysis, elevated liver enzymes, and low platelet count (HELLP) syndrome. We report a patient diagnosed with severe vitamin
Shravya Govindappagari +4 more
doaj +1 more source
Clinical case of thrombotic microangiopathy in obstetric practice
Trombotic microangiopathy is heterogeneous group of the diseases united by a community of a histological and clinical implications at difference of pathogenetic mechanisms, presents clinical-morphological syndrome characterizing a lesion of vessels of a ...
M. N. Mochalova +5 more
doaj
Ravulizumab in atypical hemolytic-uremic syndrome: a case report in a young woman with renal failure [PDF]
Atypical hemolytic-uremic syndrome (aHUS) is a rare, life-threatening, complement-mediated thrombotic microangiopathy characterized by microangiopathic hemolytic anemia, thrombocytopenia, and acute kidney injury.
Georgi Nikolov +6 more
doaj +3 more sources
Thrombotic microangiopathies: An update
Thrombotic microangiopathies (TMA) are microvascular occlusive disorders characterized by hemolytic anemia caused by fragmentation of erythrocytes and thrombocytopenia due to increased platelet aggregation and thrombus formation, eventually leading to disturbed microcirculation with reduced organ perfusion.
openaire +2 more sources
Key Clinical Message We present a case of a 23‐year‐old male who developed thrombotic microangiopathy associated with the induction dose of tacrolimus. Get an early diagnosis and give timely treatment of thrombotic microangiopathy is essential to improve
Alfredo Gutiérrez‐Govea +4 more
doaj +1 more source
The Use of Eculizumab in Tacrolimus-Induced Thrombotic Microangiopathy
Drug-induced thrombotic microangiopathy (DITMA) is a secondary cause of thrombotic microangiopathy and a potentially fatal inflammatory disease. DITMA has been attributed to a variety of drugs, particularly chemotherapeutic and immunosuppressive agents ...
Jihad Ben Gabr MD +3 more
doaj +1 more source

