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

  • Gopalarathinam R
  • Orlowsky E
  • Kesavalu R
  • et al.
N/ACitations
Citations of this article
72Readers
Mendeley users who have this article in their library.

This article is free to access.

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.

Cite

CITATION STYLE

APA

Gopalarathinam, R., Orlowsky, E., Kesavalu, R., & Yelaminchili, S. (2016). Adult Onset Still’s Disease: A Review on Diagnostic Workup and Treatment Options. Case Reports in Rheumatology, 2016, 1–6. https://doi.org/10.1155/2016/6502373

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free