Results 91 to 100 of about 1,143,866 (185)

SAPHO syndrome: Misdiagnosed and operated [Sindrome de SAPHO: Mal diagnosticado e operado] [PDF]

, 2008
SAPHO is a rare disorder that results in synovitis, acne, pustulosis, hyperostosis and osteitis. Patients with this syndrome typically present with musculoskeletal complaints, frequently localized to the anterior chest wall.

core  

Synovitis, acne, pustulosis, hyperostosis, osteitis (SAPHO) syndrome in childhood: a report of ten cases and review of the literature [PDF]

, 2000
Chronic recurrent multifocal osteomyelitis is a rare chronic inflammatory musculoskeletal process observed in children and young adults. Recently, the acronym SAPHO syndrome (for synovitis, acne, pustulosis, hyperostosis, osteitis) was coined to ...
Bianchetti, MG, Sauvain, M J, Schibler, A, Beretta-Piccoli, BC, Gal, I, Saurenmann, T, Kressebuch, H, Beretta-Piccoli, B C, Bianchetti, M G, Sauvain, MJ   +9 more
core   +2 more sources

SAPHO syndrome

BMJ Case Reports, 2019
Takanobu, Hirosawa, Shun, Kawamoto, Taro, Shimizu   +2 more
openaire   +4 more sources

Synovitis, acne, pustular lesions, hyperostosis, and osteitis syndrome associated with monoclonal gammopathy of undetermined significance: a case report

BMC Musculoskeletal Disorders
Herein, we present a case of synovitis, acne, pustular lesions, hyperostosis, and osteitis (SAPHO) syndrome in which the patient had monoclonal gammopathy.
Cheng Xu, Wenjuan Zhang, Xin Huang, Yongmei Han   +3 more
doaj   +1 more source

Painful scalp nodules in SAPHO syndrome

A girl aged 13 years presented with mild subcutaneous vertex tumefaction and localised alopecia (figure A). She was administered bisphosphonate and infliximab for SAPHO syndrome (ie, synovitis, acnea conglobata, pustulosis, hyperostosis, and osteitis ...
Triaille, Clément, Kokta, Victor, Powell, Julie, De Bruycker, Jean Jacques   +3 more
core   +1 more source

Coincidence of Behçet's disease and SAPHO syndrome.

, 2002
A young woman presented with deteriorated visual acuity due to acute retinal vasculitis. The diagnosis of Behçet's disease was made on the basis of the ophthalmologic findings and recurrent oral and genital aphthous ulcerations.
Welzl-Hinterkörner E, Caravatti M, Wiesli P, Schulthess G, Germann D, Uebelhart D   +5 more
core   +1 more source

SAPHO syndrome: current clinical, diagnostic and treatment approaches.

This review provides an overview of SAPHO (Synovitis, Acne, Pustulosis, Hyperostosis, and Osteitis), a rare autoinflammatory disease that primarily affects bones, skin, and joints.
Demirci Yildirim, Tuba, Sari, İsmail
core   +1 more source

Demographic features of the SAPHO syndrome patients and healthy controls.

, 2018
Demographic features of the SAPHO syndrome patients and healthy controls.
Wei Song (30780), Kai-Feng Xu (305907), Xin Sui (211430), Wenshuai Xu (6053291), Xinlun Tian (305900), Jian Wang (5901), Shuang Liu (8449), Wen Zhang (7555), Chen Li (54018)   +8 more
core   +1 more source

Successful treatment of SAPHO syndrome with oral abrocitinib: a case report

Journal of Dermatological Treatment
Aim SAPHO (synovitis, acne, pustulosis, hyperostosis and osteitis) syndrome is a rare autoimmune disorder characterized by typical cutaneous lesions (palmoplantar pustulosis and eruptive acne) and osteoarticular symptoms (aseptic osteomyelitis and joint ...
Zhipeng Lin, Songyi Piao, Rongxin Zhang, Chao Yu, Zhao Hou, Aoxue Wang   +5 more
doaj   +1 more source

SAPHO syndrome masquerading as metastatic bone disease.

, 2005
A 46-year-old woman who had had a right mastectomy for breast carcinoma a month before underwent bone scintigraphy. The examination revealed multiple pelvic, vertebral and sternal hot spots suggestive of bone metastases.
Duvoisin B, Theumann NH, Boubaker E, Schnyder P, Pugnale M, So A, Mouhsine E, Hoesli P, Spoletini P   +8 more
core   +1 more source