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Is palmoplantar pustulosis combined with hip involvement a SAPHO syndrome? [PDF]
Sun Q, Meng F, Chen N, Li C, Ying Z.
europepmc +1 more source
Coexistence of adult-onset Still's disease and SAPHO syndrome. [PDF]
Wang Y +6 more
europepmc +1 more source
“SAPHO syndrome and infections”
The syndrome of synovitis, acne, pustulosis, hyperostosis, osteitis (SAPHO) encompasses a broad spectrum of cutaneous manifestations associated with osteitic and hyperostotic lesions, which typically may involve the anterior chest wall (ACW). The aetiopathogenetic mechanisms as well as the nosographic framing of the disease are still not fully defined ...
Matteo Colina +2 more
exaly +4 more sources
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Rheumatic Disease Clinics of North America, 2013
SAPHO syndrome is a disorder characterized by Synovitis, Acne, Pustulosis, Hyperostosis, and Osteitis. As the osteoarticular and skin manifestations often do not occur simultaneously and there are no validated diagnostic criteria, the diagnosis can be difficult.
Sueli, Carneiro +1 more
+5 more sources
SAPHO syndrome is a disorder characterized by Synovitis, Acne, Pustulosis, Hyperostosis, and Osteitis. As the osteoarticular and skin manifestations often do not occur simultaneously and there are no validated diagnostic criteria, the diagnosis can be difficult.
Sueli, Carneiro +1 more
+5 more sources
Zeitschrift für Rheumatologie, 2014
The SAPHO syndrome, an acronym for synovitis, acne, pustulosis, hyperostosis and osteitis, is a rare disease which affects bones, joints and the skin. The main osteoarticular features are hyperostosis and osteitis. Osteoarticular symptoms predominantly occur on the anterior chest wall but the spine and the peripheral skeleton can also be involved.
F, Heldmann +3 more
openaire +3 more sources
The SAPHO syndrome, an acronym for synovitis, acne, pustulosis, hyperostosis and osteitis, is a rare disease which affects bones, joints and the skin. The main osteoarticular features are hyperostosis and osteitis. Osteoarticular symptoms predominantly occur on the anterior chest wall but the spine and the peripheral skeleton can also be involved.
F, Heldmann +3 more
openaire +3 more sources
Dermatology, 2009
Four women with pustulosis palmoplantaris (PPP) and associated sternocostoclavicular hyperostosis are described. The connection between the two diseases is not coincidental: it is encountered in 9.4% of PPP patients, and was reported in the French literature as part of the SAPHO (synovitis acne pustulosis hyperostosis osteomyelitis) syndrome.
R E, Brandsen +5 more
openaire +3 more sources
Four women with pustulosis palmoplantaris (PPP) and associated sternocostoclavicular hyperostosis are described. The connection between the two diseases is not coincidental: it is encountered in 9.4% of PPP patients, and was reported in the French literature as part of the SAPHO (synovitis acne pustulosis hyperostosis osteomyelitis) syndrome.
R E, Brandsen +5 more
openaire +3 more sources
SAPHO syndrome with ankylosis of the temporomandibular joint
SAPHO syndrome is a rare combination of different symptoms with unknown aetiology. A complete ankylosis of the temporomandibular joint (TMJ) in a patient with SAPHO syndrome has not been described previously.
Urs Müller-Richter +2 more
exaly +2 more sources

