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Aortic stenosis concomitant with microscopic polyangiitis: a challenge in medical reasoning and thinking
Paulo Sampaio Gutierrez1, Vera Demarchi Aiello1
1Laboratory of Pathology - Instituto do Coração - Hospital das Clínicas - Faculdade de Medicina - Universidade de São Paulo, São Paulo/SP - Brazil.
Abstract:
Microscopic polyangiitis (MPA) is part of the anti-neutrophil cytoplasmic antibodies (ANCA)-related vasculitis, which usually presents as renal pulmonary syndrome. It is defined as a pauci-immune necrotizing small vessel vasculitis, which usually affects the kidneys, followed by the lungs. It also presents systemic symptoms. The etiology of MPA is still unclear, but evidence reinforces the autoimmune mechanisms as the main etiopathogenic factor. Aortic valve stenosis (AS) is not an uncommon disease whose etiology varies according to geographical differences and the patient's age. The natural history of AS begins with a prolonged asymptomatic period, but when symptomatic, respiratory failure is one of its main clinical presentations. The authors present the case of a 55-year-old woman who was admitted with the diagnosis of renal failure, anemia, and a cardiac murmur. The patient had been recently diagnosed with pneumonia. During hospitalization, diagnostic workup disclosed a normal kidney size as well as parenchymal thickness. A renal biopsy was undertaken but the specimen was exiguous, showing 4 sclerotic glomeruli and 1 glomerulus with crescentic glomerulonephritis. The search for ANCA was positive. The investigation of the cardiac murmur disclosed AS. The patient, on hemodialysis, presented episodes of respiratory failure, which was interpreted as acute pulmonary edema, but a suspicion of ANCA-related pulmonary renal syndrome was raised. However, the aortic valve replacement was prioritized. While awaiting cardiac surgery, the patient died because of respiratory insufficiency. Autopsy findings concluded that MPA with pulmonary hemorrhage due to vasculitis was the immediate cause of death. Although AS was present at autopsy and classified as moderate/severe, this lesion was a bystander in the process of this patient's end of life, demonstrating the value of autopsy for medical learning and reasoning purposes.
Insights
Microscopic polyangiitis (MPA), an autoimmune vasculitis, can cause severe kidney and lung damage. This case highlights MPA
Area of Science:
- Nephrology and Rheumatology
- Cardiovascular Medicine
- Pathology
Background:
- Microscopic polyangiitis (MPA) is an anti-neutrophil cytoplasmic antibodies (ANCA)-associated small vessel vasculitis, typically affecting the kidneys and lungs.
- Aortic valve stenosis (AS) is a common cardiac condition with varied etiologies, often presenting with respiratory symptoms when severe.
- The interplay between MPA and concurrent cardiac conditions like AS can complicate diagnosis and management.
Observation:
- A 55-year-old woman presented with renal failure, anemia, and a cardiac murmur, initially suspected to have pneumonia.
- Renal biopsy revealed pauci-immune crescentic glomerulonephritis, and ANCA testing was positive, supporting MPA.
- Significant aortic valve stenosis (AS) was identified, posing a diagnostic dilemma regarding the primary cause of respiratory failure.
Findings:
- Despite prioritization of aortic valve replacement, the patient experienced fatal respiratory insufficiency.
- Autopsy confirmed microscopic polyangiitis (MPA) with pulmonary hemorrhage as the cause of death.
- The moderate-to-severe aortic valve stenosis (AS) was deemed incidental and not the primary driver of the fatal outcome.
Implications:
- This case underscores the critical role of autopsy in elucidating the true cause of death in complex multi-system diseases.
- It highlights the importance of considering ANCA-related vasculitis in patients with unexplained renal and pulmonary syndromes, even with co-existing cardiac conditions.
- Accurate diagnosis and timely management of MPA are crucial to prevent life-threatening complications, irrespective of other comorbidities.
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