Adult-Onset Still’s Disease in a 28-Year-Old Man From Ghana

Adult-onset Still’s disease is a rare, autoinflammatory disease characterized by spiking fevers, arthritis, salmon-colored skin rash, and leukocytosis. It has been compared to systemic juvenile idiopathic arthritis because of its similar features but is much rarer than its pediatric counterpart. It...

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Detalles Bibliográficos
Autores principales: Kashfi, Simon, Sharma, Sapna, Bengualid, Victoria, Sharma, Shorabh, Gandrabur, Liliya
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2021
Materias:
Internal Medicine
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8528165/
https://www.ncbi.nlm.nih.gov/pubmed/34692336
http://dx.doi.org/10.7759/cureus.18126
Descripción
Sumario:Adult-onset Still’s disease is a rare, autoinflammatory disease characterized by spiking fevers, arthritis, salmon-colored skin rash, and leukocytosis. It has been compared to systemic juvenile idiopathic arthritis because of its similar features but is much rarer than its pediatric counterpart. It is usually treated with corticosteroids and disease-modifying anti-rheumatic drugs. However, those with refractory disease are candidates for one of many biological therapies. We present the case of a 28-year-old man who was successfully managed with first-line steroid therapy.

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