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.
| SAPHO syndrome | |
|---|---|
| Other names | Synovitis-acne-pustulosis-hyperostosis-osteitis syndrome |
| Specialty | Rheumatology  |
An entity initially known as chronic recurrent multifocal osteomyelitis was first described in 1972.[1] Subsequently, in 1978,[2] several cases of 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 (an acronym for 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.
Diagnosis
editRadiologic findings
edit- 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
editBisphosphonate 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) has been tried in a 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 Cutibacterium acnes, a bacterium known for its role in acne, has been isolated from bone biopsies of SAPHO patients.[7][9]
See also
editReferences
edit- ^ Giedion A, Holthusen W, Masel LF, Vischer D (1972). "Subacute and chronic "symmetrical" osteomyelitis". Annals of Radiology. 15 (15): 329–42. PMID 4403064.
- ^ Bjorksten B, Gustavson KH, Eriksson B, et al. (1978). "Chronic recurrent multifocal osteomyelitis and pustulosis palmoplantaris". Journal of Pediatrics. 93 (2): 227–31. doi:10.1016/S0022-3476(78)80501-0. PMID 671154.
- ^ Chamot AM, Benhamou CL, Kahn MF, Beraneck L, Kaplan G, Prost A (1987). "Acne-pustulosis-hyperostosis-osteitis syndrome. Results of a national survey. 85 cases". Revue du Rhumatisme et des Maladies Osteo-Articulaires. 54 (3): 187–96. PMID 2954204.
- ^ Ichikawa J, Sato E, Haro H, Ando T, Maekawa S, Hamada Y (November 2008). "Successful treatment of SAPHO syndrome with an oral bisphosphonate". Rheumatology International. 29 (6): 713–5. doi:10.1007/s00296-008-0760-z. PMID 18998139. S2CID 151512.
- ^ Kerrison C, Davidson JE, Cleary AG, Beresford MW (October 2004). "Pamidronate in the treatment of childhood SAPHO syndrome". Rheumatology (Oxford). 43 (10): 1246–51. doi:10.1093/rheumatology/keh295. PMID 15238641.
- ^ Amital H, Applbaum YH, Aamar S, Daniel N, Rubinow A (May 2004). "SAPHO syndrome treated with pamidronate: an open-label study of 10 patients". Rheumatology (Oxford). 43 (5): 658–61. doi:10.1093/rheumatology/keh149. PMID 14983108.
- ^ a b Olivieri I, Padula A, Palazzi C (October 2006). "Pharmacological management of SAPHO syndrome". Expert Opinion on Investigational Drugs. 15 (10): 1229–33. doi:10.1517/13543784.15.10.1229. PMID 16989598. S2CID 34307641.
- ^ Scarpato S, Tirri E (2005). "Successful treatment of SAPHO syndrome with leflunomide. Report of two cases". Clinical and Experimental Rheumatology. 23 (5): 731. PMID 16173265.
- ^ Colina M, Lo Monaco A, Khodeir M, Trotta F (2007). "Propionibacterium acnes and SAPHO syndrome: a case report and literature review". Clinical and Experimental Rheumatology. 25 (3): 457–60. PMID 17631745.
Further reading
edit- SAPHO Syndrome Archived 2007-09-27 at the Wayback Machine by Mike Chang, M.D., University of Washington Department of Radiology
- Earwaker JW, Cotten A (June 2003). "SAPHO: syndrome or concept? Imaging findings". Skeletal Radiol. 32 (6): 311–27. doi:10.1007/s00256-003-0629-x. PMID 12719925. S2CID 25247507.