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Revista Colombiana de Reumatología

versión impresa ISSN 0121-8123

Resumen

CORDOBA, Juan Pablo et al. Pulmonary - renal syndrome: case series Hospital Universitario San Ignacio. Rev.Colomb.Reumatol. [online]. 2015, vol.22, n.1, pp.11-15. ISSN 0121-8123.  https://doi.org/10.1016/j.rcreu.2015.02.005.

Introduction: Pulmonary- renal syndrome (PRS) is defined as the presence of alveolar hemorrhage and rapidly progressive glomerulonephritis. It was initially described as glomerular basement membrane syndrome, although other more common causes and mechanisms are involved such as, anti-neutrophil cytoplasmic antibody-associated vasculitis (ANCA), systemic lupus erythematosus, antiphospholipid syndrome, cryoglobulinemia, and thrombotic microangiopathy. Objective: To describe the experience in the treatment of patients with PRS in our center and analyze the demographic, clinical variables, and outcomes. Methods: The databases of the Nephrology Unit and the electronic medical records of the hospital were reviewed, and a total of 14 patients with PRS between January 2009 and August 2011 were identified. Results: A total of 14 cases managed in the intensive care unit of the hospital where analyze, of which 57% were woman and the mean age was 44 years. The most frequent diagnosis was positive ANCA vasculitis in 8 patients, lupus in 4, one case of cryoglobulinemia, and other with thrombotic microangiopathy. Most of them were treated with corticosteroids and cyclophosphamide, with 10 patients also receiving plasmapheresis. The overall mortality was 66%. Conclusions: The results of 14 patients with PRS in our center are presented. The most common cause of this was positive ANCA vasculitis. It is an aggressive disease and its treatment included the use of steroids, cyclophosphamide and plasmapheresis.

Palabras clave : Rapidly progressive glomerulonephritis with pulmonary hemorrhage; Anti-neutrophil cytoplasmic antibody-associated vasculitis; Plasmapheresis Plasma exchange therapy.

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