Tag: #Vasculitis
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Resolved Atrioventricular Block and Left Ventricular Dysfunction in Wegener’s Granulomatosis
Introduction: Wegener’s granulomatosis, now known as granulomatosis with polyangiitis (GPA), is a rare but severe systemic vasculitis primarily affecting the respiratory tract and kidneys. However, cardiac involvement, though less common, can significantly impact patient outcomes. This case report explores the complete resolution of atrioventricular (AV) block and severe left ventricular dysfunction in a patient with…
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Double-Positive ANCA and Anti-GBM Vasculitis Insights from Two Case Reports
Introduction:Double-positive Anti-GBM and ANCA vasculitis represents a rare yet significant overlap in systemic vasculitis, posing unique challenges in diagnosis and management. This article summarizes key findings from two reported cases, shedding light on the clinical manifestations, histopathological features, and treatment considerations for this condition. Visit Clinical Nephrology Journal for more groundbreaking research in nephrology. Key…
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Hypocomplementemic Urticarial Vasculitic Syndrome A Rare Case of Renal Failure
Introduction Hypocomplementemic urticarial vasculitic syndrome (HUVS) is a rare autoimmune disorder characterized by chronic urticarial vasculitis, low complement levels, and multi-organ involvement. This condition often presents diagnostic challenges due to its overlapping features with systemic lupus erythematosus (SLE) and other autoimmune diseases. In a recently published case study, a 66-year-old man developed severe renal failure…
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