ISSN 1308-8734 | E-ISSN 1308-8742
Case Report
Pustulotic Arthro-Osteitis (Sonozaki Syndrome): A Case Report and Review of Literature
1 Department of Rheumatology, Adnan Menderes University, Aydın, Turkey  
Eurasian J Med 2018; 50: 53-55
DOI: 10.5152/eurasianjmed.2018.17268
Key Words: Sonozaki syndrome, pustular, osteitis, arthritis
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.

 

 

Cite this article as: Kose R, Senturk T, Sargin G, Cildag S, Kara Y.Pustulotic Arthro-Osteitis (Sonozaki Syndrome): A Case Report and Review of Literature.. Eurasian J Med 2018; 53-5.

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