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A Case of Palmoplantar Pustulosis Present in the Daughter of a SAPHO Syndrome Patient
Journal of Rheumatic Diseases ; : 127-131, 2015.
Article in Korean | WPRIM | ID: wpr-172589
ABSTRACT
SAPHO syndrome is a rare inflammatory, pseudoinfectious disease. Initially it was an acronym for Syndrome Acne Pustulosis Hyperostosis Osteitis, and the meaning of S was later changed to synovitis. It occurs predominantly in children and adults and is not common over 60 years. The most common clinical presentation is osteoarticular involvement at the anterior chest wall and skin manifestations may be evident, but it could occur years earlier or develop later. We report on two cases of mother and daughter. A 51-year-old female was diagnosed with SAPHO syndrome with costochondritis and palmoplantar pustulosis. Five years later, her 31-year-old daughter presented with similar skin manifestations of the hand and foot.
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Full text: Available Index: WPRIM (Western Pacific) Main subject: Osteitis / Psoriasis / Skin Manifestations / Synovitis / Nuclear Family / Hyperostosis / Acne Vulgaris / Acquired Hyperostosis Syndrome / Thoracic Wall / Foot Limits: Adult / Child / Female / Humans Language: Korean Journal: Journal of Rheumatic Diseases Year: 2015 Type: Article

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Full text: Available Index: WPRIM (Western Pacific) Main subject: Osteitis / Psoriasis / Skin Manifestations / Synovitis / Nuclear Family / Hyperostosis / Acne Vulgaris / Acquired Hyperostosis Syndrome / Thoracic Wall / Foot Limits: Adult / Child / Female / Humans Language: Korean Journal: Journal of Rheumatic Diseases Year: 2015 Type: Article