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Órgano Científico Oficial de SOCIEM-UCV

2007, Number 4

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Acta Cient Estud 2007; 5 (4)

Displasia Osteofibrosa Costal. A Propósito De Un Caso Clínico

Bousquet JR, Granado Á, Bousquet JA, Rodríguez I, Charcousse Y

Language: Spanish
References: 14
Page: 178-185
PDF size: 313.09 Kb.


ABSTRACT

Costal osteo-fibrous dysplasia is idiopathic pathology of the skeleton, in which the marrow of some bones is replaced by fibrous and bony weave disorganized, with trabeculae of immature, devoid bone of osteoblastos. They have predilection by the long bones, ribs, and craniofacial bones. It can imply a bone (monostotic), multiple bones (polyostotic), and a polyostotic form accompanied by abnormalitys endocrines, like precocious puberty, premature skeletal maturation or hyperthyroidism, well-known set at the moment like disease of Albrighty. Objective: To inform the case into a masculine patient of 60 years of age, carrier of costal tumors. Method: Description of the clinical case and revision of Literature. Atmosphere: Department of Surgery. University Hospital Dr Luis Razetti. Barcelona. Anzoátegui State. Result: It was come to make Right Axillary Toracotomía with inferior anterior extension by costal tumors. Conclusion: The great majority of the injuries is asymptomatic, affects to a single bone (monostotic variety) and they have been discovered accidentally. The surgery this indicated for taking of confirmatory biopsy, correction of the deformity, prevention of pathological fractures and/or the extirpation of symptomatic injuries.


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