Abstract
Acute Granulomatous Polyangiitis (AGPA), known as Wegener,’s granulomatosis, is a rare and multi-systemic disease that causes medium and small vessel inflammation. It appears initially during adolescence from 15 to 16 years of age, affecting primarily the upper respiratory tract, the lungs and kidneys. This is the case of a male, 15 year old symptomatic and paraclinical tests suggestive of pneumonia; the patient evolved to ARDS and diffuse refractory alveolar bleeding.
References
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