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A case of pulmonary hemorrhage and renal failure

dc.contributor.authorMeara, Alexa S.
dc.contributor.authorHarrington, Daphne M.
dc.contributor.authorFoster, Jennifer
dc.contributor.authorVachharajani, Tushar J.
dc.contributor.authorDesai, Tejas
dc.date.accessioned2020-04-02T17:54:05Z
dc.date.available2020-04-02T17:54:05Z
dc.date.issued2012-12-14
dc.description.abstractBackground: Alveolar hemorrhage can be seen in many vasculitic disorders. However, granulomatosis polyangiitis (formerly Wegener’s granulomatosis) uncommonly presents with life threatening alveolar hemorrhage and has only been discussed in a few case reports [1]. Case Presentation: A 53 year old Caucasian male presented with hemoptysis and profound anemia. Two weeks prior, he had presented with abdominal pain with normal renal function and numerous pulmonary nodules. During the current admission, the patient was hypoxic with acute renal failure requiring hemodialysis. Urine sediment demonstrated dysmorphic red blood cells. A bronchoscopy revealed diffuse alveolar hemorrhage. The diagnosis of pulmonary-renal syndrome was made and therapeutic plasma exchange was initiated. Laboratory studies were significant for a c-ANCA titer positive at 1:640 FIU and anti-proteinase (PR)-3 antibody titer positive with 78.3 U/ml. Renal biopsy demonstrated necrotizing crescentic glomerulonephritis. A diagnosis of granulomatosis vasculitis was determined. Conclusion: Alveolar hemorrhage is rare to be the presenting symptom of granulomatosis vasculitis where the common presenting features are recurrent sinusitis, epistaxis, chronic otitis media or rhinitis. Physicians should consider granulomatosis vasculitis in the differential diagnosis of pulmonary-renal syndrome presenting with hemoptysis.en_US
dc.identifier.doi10.2174/1874303X01205010040
dc.identifier.urihttp://hdl.handle.net/10342/7762
dc.titleA case of pulmonary hemorrhage and renal failureen_US
dc.typeArticleen_US
ecu.journal.issue1en_US
ecu.journal.nameThe Open Urology & Nephrology Journalen_US
ecu.journal.pages40-47en_US
ecu.journal.volume5en_US

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