Abstract Number: 1248 • 2019 ACR/ARP Annual Meeting
Clinical Manifestations and Management of US Patients with SAPHO (Synovitis, Acne, Pustulosis, Hyperostosis, Osteitis) Syndrome, a Retrospective Study
Background/Purpose: The SAPHO syndrome is a rare inflammatory disorder of bones, joints and skin first coined by Chamot in 1987 characterized by synovitis, acne, pustulosis,…Abstract Number: 1259 • 2019 ACR/ARP Annual Meeting
Synovitis, Acne, Pustulosis, Hyperostosis, and Osteitis (SAPHO): A Case Series
Background/Purpose: SAPHO is a chronic multisystemic illness with predominantly skin and joint manifestations. Disease presentation is heterogenous; proposed diagnostic criteria include chronic multifocal aseptic osteomyelitis…Abstract Number: 371 • 2017 ACR/ARHP Annual Meeting
Longer Term Outcomes of Chronic Relapsing Multifocal Osteomyelitis in a UK Tertiary Adolescent and Young Adult Rheumatology Centre
Background/Purpose: Chronic relapsing multifocal osteomyelitis (CRMO) is a rare autoinflammatory bone condition presenting primarily in children & adolescents. It characteristically affects the epiphysis & metaphysis…Abstract Number: 1883 • 2017 ACR/ARHP Annual Meeting
Patterns of Osteoarticular Involvement in SAPHO Syndrome: A Cluster Analysis Based on Whole Body Bone Scintigraphy in 157 Patients
Background/Purpose: The aim was to explore patterns of osteoarticular involvement in SAPHO syndrome using cluster analysis of lesions revealed by whole body bone scintigraphy. Methods:…Abstract Number: 1367 • 2012 ACR/ARHP Annual Meeting
Clinical Features and Treatment Results of Japanese Patients with SAPHO (Synovitis-Acne-Pustulosis-Hyperostosis-Osteitis) Syndrome
Background/Purpose: SAPHO syndrome is a disorder characterized by pustular skin lesions and osteoarticular lesions, which was proposed by Chamot et al. in 1987. Clinical studies…