30-176
Osteopoiquilosis y síndrome de Buschke-Ollendörf.
Osteopoikilosis and buschke-ollendórf disease. Case report
A. ARRANZ ROA, A. BLANCO POZO, E. MADERO MADERO, J. ARTECHE DEL LLANO y J. CAMATS FRANCO Servicio de Cirugía Ortopédica y Traumatología. Hospital «General Yagüe». Burgos.
Recepción:
06/11/2008
Aceptación:
06/11/2008
Publicación:
06/11/2008
Métricas
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Resumen (ES)
A female patient, 22 years oíd, showing characteristic sclerotic bone images on
radiographic examinations is reported. The main locations were on the distal limbs and pelvis.
She has also elastic nevi as freckles in the skin. This entity was not stablished as inhered process.
The differential diagnosis lies between sclerotic metastasis, neurofibromatosis (Von Recklinghausen),
Bourneville disease and other displastyc lesions.
radiographic examinations is reported. The main locations were on the distal limbs and pelvis.
She has also elastic nevi as freckles in the skin. This entity was not stablished as inhered process.
The differential diagnosis lies between sclerotic metastasis, neurofibromatosis (Von Recklinghausen),
Bourneville disease and other displastyc lesions.
Palabras clave (ES):
Buscke-Ollendörf
Síndrome
Osteopoiquilosis
Osteopoiquilia
Displasia
Ósea
Resumen (EN)
A female patient, 22 years oíd, showing characteristic sclerotic bone images on
radiographic examinations is reported. The main locations were on the distal limbs and pelvis.
She has also elastic nevi as freckles in the skin. This entity was not stablished as inhered process.
The differential diagnosis lies between sclerotic metastasis, neurofibromatosis (Von Recklinghausen),
Bourneville disease and other displastyc lesions.
radiographic examinations is reported. The main locations were on the distal limbs and pelvis.
She has also elastic nevi as freckles in the skin. This entity was not stablished as inhered process.
The differential diagnosis lies between sclerotic metastasis, neurofibromatosis (Von Recklinghausen),
Bourneville disease and other displastyc lesions.
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