Adult Onset Still’s Disease: A Review on Diagnostic Workup and Treatment Options

Author:

Gopalarathinam Rajesh1,Orlowsky Eric2,Kesavalu Ramesh3,Yelaminchili Sreeteja4

Affiliation:

1. Department of Internal Medicine, Allegheny General Hospital, 320 E. North Avenue, Pittsburgh, PA 15212, USA

2. Department of Rheumatology, Allegheny General Hospital, 320 E. North Avenue, Pittsburgh, PA 15212, USA

3. Department of Rheumatology, Lakeside Community Healthcare Medical Group, 1500 S. Central Avenue No. 200, Glendale, CA 91204, USA

4. Department of Internal Medicine, Capital Health Regional Medical Center, 750 Brunswick Avenue, Trenton, NJ 08638, USA

Abstract

Adult onset Still’s disease (AOSD) is a rare systemic inflammatory disease of unknown etiology and pathogenesis that presents in 5 to 10% of patients as fever of unknown origin (FUO) accompanied by systemic manifestations. We report an interesting case of a 33-year-old African-American male who presented with one-month duration of FUO along with skin rash, sore throat, and arthralgia. After extensive workup, potential differential diagnoses were ruled out and the patient was diagnosed with AOSD based on the Yamaguchi criteria. The case history, incidence, pathogenesis, clinical manifestations, differential diagnoses, diagnostic workup, treatment modalities, and prognosis of AOSD are discussed in this case report.

Publisher

Hindawi Limited

Subject

General Agricultural and Biological Sciences

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