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Cuad. Hosp. Clín ; 52(2): 82-85, 2007. ilus
Article in Spanish | LILACS | ID: lil-784075

ABSTRACT

La enfermedad de Ollier es una encondromatosis múltiple querepresenta el 3 % de los tumores óseos benignos. Las encodromatosisson tumores cartilaginosos que pueden ensanchar el hueso yproducir la clásica característica de la calcifi cación moteada dentrode las lesiones. Se presenta el caso de un escolar masculino de6 años de edad con presencia de múltiples encondromas en lasextremidades torácicas y pélvicas derechas (húmero- radio y cubito,falanges de la mano, fémur, tibia, peroné, y falanges del pie), quehan producido deformidades angulares, rotacionales y asimetría deextremidades pélvicas, que han sido tratadas con osteotomías yfi jación externa tipo Ilizarow a nivel del defecto tumoral en la Unidadde Ortopedia pediátrica del Hospital del Niño de La Paz-Bolivia.


Ollier’s disease is a multiple enchondromatose which constitutes3% of benign bone tumors. Enchondromatoses can thicken thebone and produce the classical characteristics of the cartilaginoustumors: spotted calcifi cations within the lesion. I present the caseof a six year-old school boy who had multiple enchondromes in theright thoracic and pelvic extremities (humero-radius and cubitus,phalanges of the hand, femur, tibia, fi bula, and phalanges of the foot).that had produced angular, rotational deformities and asymmetry ofthe pelvic extremities which had been treated with osteotomy andexternal fi xation according to IIizarow at the level of the tumorousdefect, in the Unit of Pediatric Orthopedics of the Children’s Hospitalin La Paz, Bolivia.


Subject(s)
Humans , Male , Child , Enchondromatosis/pathology , Fractures, Spontaneous , Femoral Fractures , Bone Diseases, Developmental , Enchondromatosis
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