A Case of Palmoplantar Pustulosis Present in the Daughter of a SAPHO Syndrome Patient
Journal of Rheumatic Diseases
; : 127-131, 2015.
Article
en Ko
| WPRIM
| ID: wpr-172589
Biblioteca responsable:
WPRO
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.
Palabras clave
Texto completo:
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Índice:
WPRIM
Asunto principal:
Osteítis
/
Psoriasis
/
Manifestaciones Cutáneas
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Sinovitis
/
Núcleo Familiar
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Hiperostosis
/
Acné Vulgar
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Síndrome de Hiperostosis Adquirido
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Pared Torácica
/
Pie
Límite:
Adult
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Child
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Female
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Humans
Idioma:
Ko
Revista:
Journal of Rheumatic Diseases
Año:
2015
Tipo del documento:
Article