Results 41 to 50 of about 61,384 (225)
Thrombotic microangiopathy etiologies.
Thrombotic microangiopathy etiologies.
Aina Obrador Mulet (5925170) +14 more
core +1 more source
Thrombotic microangiopathy encompasses microvascular thrombosis, hemolytic anemia, thrombocytopenia, and end-organ damage. Secondary thrombotic microangiopathy can result from malignancies, autoimmune diseases, or treatments such as tyrosine kinase ...
Ryan Sabour +6 more
doaj +1 more source
Complement Activation Linked to Type II Interferon Signaling in Still Disease
Objective Still disease (SD) is an autoinflammatory syndrome characterized by innate immune dysregulation. Although complement can drive inflammation, its involvement in SD remains to be defined. Thus, we aimed to assess complement activation in SD. Methods Complement was assessed using transcriptomic, proteomic, and in vitro approaches. RNA sequencing
Freya M. C. H. Huijsmans +115 more
wiley +1 more source
Drug Induced Thrombotic Microangiopathy Caused by Levofloxacin
Thrombotic microangiopathy is a rare but serious manifestation of a variety of diseases. The key features are microangiopathic haemolysis, thrombocytopaenia, renal dysfunction and neurological symptoms. Here we discuss the case of a previously well male
GC Preston, S Kazi
core +1 more source
COVID-19 Microangiopathy: Insights into plasma exchange as a therapeutic strategy
COVID-19-associated thrombotic microangiopathy has emerged as a severe complication that exacerbates morbidity and mortality in critical cases. Thrombotic microangiopathy, characterized by microvascular thrombosis and endothelial injury, includes ...
Yigit Baykara, Kaan Sevgi, Yamac Akgun
doaj +1 more source
Pulmonary tumor thrombotic microangiopathy successfully treated with corticosteroids: a case report
Background Pulmonary tumor thrombotic microangiopathy is a special type of tumor thromboembolism. We report the case of a patient who developed pulmonary tumor thrombotic microangiopathy with alveolar hemorrhage.
Shinichi Miyazaki +6 more
doaj +1 more source
CHAPLE‐Like Enteropathy and Renal Microangiopathy in an Adult Patient With CD46 Deficiency
We report an adult patient with a homozygous CD46 variant presenting with lifelong protein‐losing enteropathy, intestinal lymphangiectasia, and CVID‐like hypogammaglobulinemia mimicking CHAPLE syndrome. Concurrent renal biopsy revealed PLA2R‐negative membranous nephropathy with chronic thrombotic microangiopathy, establishing multi‐organ complement ...
Bircan Erden +14 more
wiley +1 more source
How I treat thrombotic thrombocytopenic purpura and atypical haemolytic uraemic syndrome [PDF]
Thrombotic thrombocytopenic purpura (TTP) and atypical haemolytic uraemic syndrome (aHUS) are acute, rare life-threatening thrombotic microangiopathies that require rapid diagnosis and treatment.
Goodship, T, Scully, M
core
We report on a 3-month old infant male who had a seven-days history of fever and rhinorrhea associated with wheezing prior to his death, during the Covid-19 pandemic.
Hubert Daisley Jr +4 more
doaj
Elevated troponin was associated with poor prognosis during thrombotic microangiopathy (TMA) in several reports, but elevated troponin in haploidentical hematopoietic stem cell transplantation-associated thrombotic microangiopathy (TATMA) has not yet ...
Lili Zhou +4 more
doaj +1 more source

