[Juvenile Sapho a two cases reports]
Revue Maghrebine de Pediatrie [La]. 2008; 18 (1): 39-42
en Francés
| IMEMR
| ID: emr-108753
ABSTRACT
The acronym Sapho syndrome [for synovitis, acne, pustulosis, hyperostosis, osteitis] is a rare entity, particulary in pediatric patients. A 15 year-old and 19 year-old adolescents, with severe acne history, presented inflammatory buttock pain associated to lumbar pain in the first case and sternal pain in the second. Radiographic exploration demonstrated bilateral sacro-iliitis associated to sterno-clavicle arthritis in the second case. Diagnosis of Sapho syndrome was retained. Satisfactory improvement was caused by corticosteroids in the first case and non steroidal anti-inflammatory drugs in the second. Sapho syndrome is rare disease with unknown origin. Non steroidal anti-inflammatory drugs are the treatment of choice, as they are usually both effective and well tolerated
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Índice:
IMEMR (Mediterraneo Oriental)
Asunto principal:
Síndrome de Hiperostosis Adquirido
/
Sacroileítis
Tipo de estudio:
Informe de Casos
Límite:
Humanos
/
Masculino
Idioma:
Francés
Revista:
Rev. Maghreb. Pediatr.
Año:
2008
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