Abstract
Adult-onset Still's disease is a rare autoimmune disorder accompanied by a triad of fever, exanthema, and arthralgia. In addition to this dominant presentation, it has a wide spectrum of clinical symptoms, with extensive involvement of multiple organs. Because of this diagnostic of adult-onset Still's disease remains one of exclusion and fulfilling sets of diagnostic criteria
We report on the case of a 20-year-old female who was initially treated for a suspected allergic reaction to a drug and then referred to an infectious disease specialist as Fever of unknown origin accompanied with rash.
Keywords
Array
DOI:
10.5937/mckg57-48282
References
Downloads
Download data is not yet available.