Results 11 to 20 of about 207 (110)

Sternocostoclavicular Hyperostosis: An Ill-Recognized Disease. [PDF]

open access: yesDiagnostics (Basel), 2016
Sternocostoclavicular hyperostosis (SCCH) is an ill-recognized, rarely diagnosed disease. Today, SCCH is widely considered part of the synovitis, acne, pustulosis, hyperostosis and osteitis (SAPHO) syndrome. SCCH develops over years with intermittent attacks of pain, swelling, and reddening of the sternocostoclavicular region.
Roed B   +4 more
europepmc   +3 more sources

Immunological Characterization of Chronic Nonbacterial Osteomyelitis (CNO) in Adults: A Cross-Sectional Exploratory Study. [PDF]

open access: yesJBMR Plus, 2023
Generic inflammation parameters like ESR, CRP, platelet and neutrophil count are relatively increased in our adult CNO cohort compared to healthy controls, but stay within absolute reference range. Within patients, vertebral involvement and skin inflammation are associated with more pronounced systemic inflammation as compared to isolated bone ...
Leerling AT   +6 more
europepmc   +2 more sources

Enteropathic SAPHO Syndrome in Ulcerative Colitis Responsive to Bisphosphonates. [PDF]

open access: yesCase Rep Rheumatol
SAPHO syndrome, a rare inflammatory disorder of bone, joints, and skin, is named based on the presence of synovitis, acne, pustulosis, hyperostosis, and osteitis. The hallmark of SAPHO syndrome includes osteoarticular and dermatologic manifestations, however, rarer associations with inflammatory bowel disease (particularly Crohn’s disease) have been ...
Phillipps J   +6 more
europepmc   +2 more sources

Synovitis, Acne, Pustulosis, Hyperostosis, and Osteitis Syndrome with Purely Osteolytic, Not Osteosclerotic, Lesions Mimicking a Malignant Tumor. [PDF]

open access: yesCase Rep Rheumatol, 2020
Synovitis, acne, pustulosis, hyperostosis, and osteitis (SAPHO) syndrome is a rare inflammatory disorder with multiple phenotypes. The syndrome has identifiable radiologic characteristics that are the most important when making a diagnosis. X‐rays of cases diagnosed with SAPHO syndrome reveal sclerotic lesions or mixed lytic and sclerotic lesions. Pure
Kinoshita H   +9 more
europepmc   +2 more sources

Stress fracture of the midshaft clavicle associated with sternocostoclavicular hyperostosis—Case report [PDF]

open access: yesInternational Journal of Surgery Case Reports, 2019
Shuichi Miyamoto   +2 more
exaly   +2 more sources

SAPHO Syndrome in Crohn’s Disease Successfully Treated with Ustekinumab: Case Report and Review of the Literature

open access: yesEuropean Medical Journal Gastroenterology, 2023
The authors report a case of synovitis, acne, pustulosis, hyperostosis, osteitis (SAPHO) syndrome in a patient with Crohn’s disease (CD). SAPHO syndrome is a rare disease characterised by the association, even if not simultaneous, of joint and skin ...
Sara Caporuscio   +4 more
doaj   +1 more source

Sternocostoclavicular Hyperostosis [PDF]

open access: yesYonsei Medical Journal, 1988
Stemocostoclavicular hyperostosis (SCCH) is a very uncommon disease characterized by hyperostosis of the clavicle, upper ribs, sternum and soft tissue ossification, particularly of the costoclaviculr ligament. Although the cause of this disorder is unknown, clinical, radiological and histological examinations may allow the diagnosis of SCCH. This paper
J S, Suh   +3 more
openaire   +3 more sources

Similarities and Differences between Clavicular Bacterial Osteomyelitis and Nonbacterial Osteitis: Comparisons of 327 Reported Cases

open access: yesJournal of Immunology Research, Volume 2021, Issue 1, 2021., 2021
Background. Currently, both clavicular bacterial osteomyelitis (BO) and nonbacterial osteitis (NBO) remain not well understood owing to their much lower incidences. This study is aimed at summarizing similarities and differences between clavicular BO and NBO based on comparisons of literature‐reported cases. Methods.
Nan Jiang   +5 more
wiley   +1 more source

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