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Pulmonary Microscopic Polyangiitis Presenting as Acute Respiratory Failure from Diffuse Alveolar Hemorrhage
Katharine K Roberts1, Michael M Chamberlin, Allen R Holmes
1San Antonio Military Medical Center. katharine.k.roberts.mil@mail.mil.
Abstract:
Microscopic polyangiitis and granulomatosis with polyangiitis are rare anti-neutrophilic cytoplasmic antibody-associated systemic vasculitides that predominantly affect small to medium sized vessels of the lungs and kidneys. These syndromes are largely confined to older adults and often present sub-acutely following weeks to months of nonspecific prodromal symptoms. While both diseases often manifest within multiple organ systems concurrently, the disease spectrum of microscopic polyangiitis almost always includes the kidneys, while granulomatosis with polyangiitis is most commonly associated with pulmonary disease. We present two cases of rapid onset respiratory failure secondary to diffuse alveolar hemorrhage in young active duty military personnel. After serological testing and surgical lung biopsy, both patients were diagnosed with microscopic polyangiitis with isolated pulmonary involvement.
Insights
Microscopic polyangiitis, a rare vasculitis, can cause rapid respiratory failure in young adults. This study highlights two military personnel diagnosed with isolated pulmonary microscopic polyangiitis.
Area of Science:
- Rheumatology
- Pulmonology
- Pathology
Background:
- Microscopic polyangiitis (MPA) and granulomatosis with polyangiitis (GPA) are rare anti-neutrophilic cytoplasmic antibody-associated vasculitides.
- These conditions primarily affect small to medium-sized vessels in the lungs and kidneys, typically in older adults with subacute onset.
- MPA commonly involves kidneys, while GPA is associated with pulmonary disease.
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