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10.1155/2017/6501738

http://scihub22266oqcxt.onion/10.1155/2017/6501738
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C5585673!5585673!28912820
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suck abstract from ncbi


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pmid28912820      Case+Rep+Med 2017 ; 2017 (ä): ä
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  • Granulomatosis with Polyangiitis with Myocarditis and Ventricular Tachycardia #MMPMID28912820
  • Hanna RM; Lopez E; Wilson J
  • Case Rep Med 2017[]; 2017 (ä): ä PMID28912820show ga
  • Granulomatosis with polyangiitis (GPA), previously known as Wegener's granulomatosis, is a pulmonary-renal syndrome affecting small and medium sized blood vessels. The disease has a prevalence in studies ranging from 3 to 15.7 cases per 100,000, with a noted increasing incidence and prevalence in more recent studies. Pulmonary manifestations include hemorrhage, lung cavitary lesions, and pulmonary fibrosis. Within the kidney, GPA is known to cause rapidly progressive pauci-immune crescentic glomerulonephritis. Rare and severe cardiovascular manifestations include pericarditis, arrhythmias, myocarditis, and aortic valve disease. Our patient is a 43-year-old female with typical pulmonary and renal lesions from GPA and also acute myocarditis, multiple episodes of ventricular tachycardia, and a severe reactive thrombocytosis.
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