SESSION TITLE: Pulmonary Manifestations of Systemic Disease 1 SESSION TYPE: Affiliate Case Report Poster PRESENTED ON: Tuesday, October 31, 2017 at 01:30 PM - 02:30 PM INTRODUCTION: Amyloidosis is a term used to describe a group of protein folding disorders. One form of systemic amyloidosis is amyloid A-type (AA). It is known to occur in chronic inflammatory conditions, including rheumatoid arthritis (RA). The prevalence of secondary amyloidosis in patients with RA ranges from 5-78% with only a small portion of cases with biopsy proven pulmonary amyloidosis.1,2 Here we present a patient with newly diagnosed RA found to have pulmonary amyloidosis. CASE PRESENTATION: Patient is a 76 year old woman with a past medical history of asthma, hypertension, hypothyroidism, and recurrent sinusitis who presented with complaints of swelling and joint pain bilaterally in her hands, shoulders, hips, and knees of 3-4 weeks duration. She reported difficulty rising from a chair as well as lifting her arms above shoulder level. Additionally, the patient complained of a minimally productive cough with clear sputum of 2-3 weeks duration. Review of systems was positive for fatigue, weakness, dry eyes, dry mouth, and joint pain. Physical exam was notable for pain on passive ROM and decreased ROM of bilateral upper extremities; there was no tenderness to palpation over her hands. Lab work up demonstrated positive rheumatoid factor, ANA, Smith, RNP, CCP, and SSA/RO. An x-ray of the hands demonstrated normal joint spaces bilaterally and no evidence of erosive changes. A chest x-ray demonstrated multiple pulmonary nodules in both lungs. Chest CT with IV contrast demonstrated diffuse pulmonary mass lesions without cavitations. Biopsy of a peripheral lung nodule demonstrated eosinophilic material consistent with amyloid. Congo red stain confirmed the presence of amyloid. A work up for amyloidosis showed normal urine protein, normal kappa/lambda ratio, and SPEP with no monoclonal spike. The patient was started on hydroxychloroquine 200 mg BID and prednisone 20mg daily with significant improvement in swelling and joint pain. DISCUSSION: Secondary amyloidosis occurs after several years in an inflammatory state. Deposition of the precursor protein, serum amyloid A, most commonly occurs in the kidneys and gastrointestinal tract.3 Pulmonary amyloidosis is an exceedingly rare finding in RA. CONCLUSIONS: Although AA amyloidosis has become less common due to advances in the treatment of RA, clinicians should include pulmonary amyloidosis in the differential when patients with RA present with pulmonary nodules. Reference #1: Barile L, Ariza R, Muci H, et al. Tru-cut needle biopsy of subcutaneous fat in the diagnosis of secondary amyloidosis in rheumatoid arthritis. Archives of Medical Research. 1993; 189-192. Reference #2: Kobayashi H, Tada S, Fuchigami T, et al. Secondary amyloidosis in patients with rheumatoid arthritis: diagnostic and prognostic value of gastroduodenal biopsy. British Journal of Rheumatology. 1996; 44-49. Reference #3: Lachmann HJ, Goodman HJB, Gilbertson JA, et al. Natural History and Outcome in Systemic AA Amyloidosis. New England Journal of Medicine. 2007: 2361-2371. DISCLOSURE: The following authors have nothing to disclose: Hooman Saberinia, Richa Bhardwaj, Justin Goralnik, Prashant Grover No Product/Research Disclosure Information