A systemic disease that mimics a severe pulmonary infection
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Keywords

Poliangeítis granulomatosa aguda
Enfermedad de Wegener
Hemorragia alveolar
Neumonía
SDRA Acute granulomatous poliangiitis
Wegener’s disease
Alveolar bleeding
Pneumonia
ARDS

How to Cite

Vega La Rotta , G. ., Olierserra, T. ., Arboleda , G. ., & Alvarado, C. . (2014). A systemic disease that mimics a severe pulmonary infection: Acute granulomatous polyangiotis. Case report. Revista Médica Sanitas, 17(3), 159-166. Retrieved from //revistas.unisanitas.edu.co/index.php/rms/article/view/357

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.

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References

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