| Literature DB >> 29531495 |
Reyhan Kose1, Taskin Senturk1, Gokhan Sargin1, Songul Cildag1, Yasemin Kara1.
Abstract
Pustulotic arthro-osteitis (PAO) is a rare chronic inflammatory disease, which has now been classified as a seronegative spondyloarthritis. The sternoclavicular and sternocostal joints, pelvis, vertebra, hip, and long bones are affected. Skin findings of the disease are accepted as a variant of pustular psoriasis, but some authors have suggested that palmoplantar pustulosis (PPP) is a different entity. The synovitis, acne, pustulosis, hyperostosis, and osteitis (SAPHO) syndrome should be considered in the differential diagnosis. PAO differs from SAPHO by the absence of hyperostosis and the difference in skin manifestations. Here, we aimed to present a 34-year-old female patient with a diagnosis of PAO with typical skin findings and joint involvement.Entities:
Keywords: Sonozaki syndrome; arthritis; osteitis; pustular
Year: 2018 PMID: 29531495 PMCID: PMC5843456 DOI: 10.5152/eurasianjmed.2018.17268
Source DB: PubMed Journal: Eurasian J Med ISSN: 1308-8734