SAPHO syndrome
| SAPHO syndrome | |
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| Classification and external resources | |
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| DiseasesDB | 30718 |
| Patient UK | SAPHO syndrome |
SAPHO syndrome includes a variety of inflammatory bone disorders that may be associated with skin changes. These diseases share some clinical, radiologic, and pathologic characteristics.
An entity initially known as chronic recurrent multifocal osteomyelitis (CRMO) was first described in 1972.[1] Subsequently, in 1978,[2] several cases of CRMO were associated with blisters on the palms and soles (palmoplantar pustulosis). Since then, a number of associations between skin conditions and osteoarticular disorders have been reported under a variety of names, including sternocostoclavicular hyperostosis, pustulotic arthro-osteitis, and acne-associated spondyloarthropathy. The term SAPHO (synovitis, acne, pustulosis, hyperostosis, osteitis) was coined in 1987[3] to represent this spectrum of inflammatory bone disorders that may or may not be associated with dermatologic pathology.
Definition
- Synovitis
- Acne — commonly involving the face and upper back.
- Pustulosis — usually involving the palms of the hands and/or soles of the feet (palmo-plantar pustulosis).
- Hyperostosis
- Osteitis
Radiologic findings
- Anterior chest wall (most common site, 65–90% of patients):[citation needed] Hyperostosis, sclerosis and bone hypertrophy especially involving the sternoclavicular joint, often with a soft tissue component.
- Spine (33% of patients):[citation needed] Segmental, usually involving the thoracic spine. The four main presentations include spondylodiscitis, osteosclerosis, paravertebral ossifications, and sacroiliac joint involvement.
- Long bones (30% of patients):[citation needed] usually metadiaphyseal and located in the distal femur and proximal tibia. It looks like chronic osteomyelitis but will not have a sequestrum or abscess.
- Flat bones (10% of patients):[citation needed] mandible and ilium.
Peripheral arthritis has been reported in 92% of cases of SAPHO as well.[citation needed]
In children, the SAPHO syndrome is most likely to affect the metaphysis of long bones in the legs (tibia, femur, fibula), followed by clavicles and spine.
Treatment
Bisphosphonate therapy has been suggested as a first-line therapeutic option in many case reports and series.[4][5][6]
Treatment with tumor necrosis factor alpha antagonists (TNF inhibitors) have been tried in few patients with limited success.[7] Other drugs that are used in psoriatic arthritis, to which SAPHO syndrome is closely related, have also been used in this condition. They include NSAIDs, corticosteroids, sulfasalazine, methotrexate, ciclosporin and leflunomide.[8]
Some patients have responded to antibiotics. The rationale for their use is that Propionibacterium acnes, a bacterium known for its role in acne, has been isolated from bone biopsies of SAPHO patients.[7][9]
See also
References
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- SAPHO Syndrome by Mike Chang, M.D., University of Washington Department of Radiology
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- MedicineNet.com
