SESSION TITLE: Fellows Pulmonary Manifestations of Systemic Disease Posters SESSION TYPE: Fellow Case Report Posters PRESENTED ON: October 18-21, 2020 INTRODUCTION: A 78-year-old male with history of aortic sclerosis and anemia was admitted with two weeks of dyspnea, profound weakness, cough, and orthopnea On presentation he was afebrile and hemodynamically stable with normal oxygen saturations but was notably tachypneic which improved on simple nasal cannula On exam he had bilateral crackles to auscultation posteriorly with no peripheral edema Labs revealed hemoglobin 5 6g/dL with MCV 112 1, new acute kidney injury with creatinine 1 8mg/dL, and mildly elevated total and indirect bilirubin B-type natriuretic peptide was 518pg/mL Chest x-ray showed bilateral left greater than right hazy opacities CASE PRESENTATION: Initial concern was for Covid-19 with superimposed bacterial pneumonia Despite broad-spectrum antibiotics he declined over the following two days and was ultimately intubated He was noted to have a small blood clot in his posterior oropharynx at intubation Following two negative Covid-19 rt-PCR he underwent bronchoscopy with BAL that showed no blood in large airways but grossly bloody lavage return from right middle lobe and lingula Further workup was significant for elevated CRP (150 mg/dL), ANA 1:320 (homogenous) with weakly positive anti-histone antibodies, elevated anticardiolipin and anti-beta-2 microglobulin IgM, and positive p-ANCA with titer 1:640 and elevated anti-MPO and anti-PR3 Due to worsening creatinine he underwent renal biopsy which revealed crescentic necrotizing glomerulonephritis without thrombotic microangiopathy, and with IgG and C3 deposition After initiation of high dose steroids and rituximab the patient rapidly improved, was extubated and transferred to the floor Plasma exchange was deferred due to stabilization Further chart review revealed that he had been taking hydralazine for several years in increasing doses, most recently increased two months prior to his presentation DISCUSSION: Diffuse alveolar hemorrhage should be suspected in patients with systemic symptoms, anemia, and pulmonary infiltrates High dose steroids should be empirically started if there is high suspicion for inflammatory cause, particularly in the presence of concurrent renal dysfunction Immunomodulatory agents such as cyclophosphamide or rituximab should then be initiated based on serologies or pathology, as well as plasma exchange in patients with rapidly declining renal function or diffuse alveolar hemorrhage with respiratory compromise CONCLUSIONS: Unexpected overlap in rheumatologic markers should prompt consideration of drug-induced vasculitis Hydralazine induced vasculitis in particular is commonly associated with dual ANCA positivity with concurrent antiphospholipid and antihistone antibodies Renal biopsy shows pauci-immune crescentic glomerulonephritis and may also show IgM, IgG and C3 deposits without immune complexes Management consists of halting the offending agent and long-term immunosuppression Reference #1: Babar, F , Posner, J N , & Obah, E A (2016) Hydralazine-induced pauci-immune glomerulonephritis: intriguing case series with misleading diagnoses Journal of community hospital internal medicine perspectives, 6(2), 30632 Reference #2: Dobre, M , Wish, J , & Negrea, L (2009) Hydralazine-induced ANCA-positive pauci-immune glomerulonephritis: a case report and literature review Renal failure, 31(8), 745-748 DISCLOSURES: No relevant relationships by Natalie Achamallah, source=Web Response