Fibrous dysplasia of bone (Q44580): Difference between revisions

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A displasia fibrosa do osso é uma doença óssea benigna, congênita, não hereditária, na qual o osso normal é substituído por um tecido semelhante à fibrose, com osteogênese imatura. Lesões ósseas são mono ou poliostóticas e podem associar-se à dor e fragilidade, levando a fraturas. Em alguns pacientes ou localizações ósseas, as lesões são hipertróficas e podem levar a complicações neurológicas.
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Fibrous dysplasia of bone is a congenital non-hereditary benign bone disease, where normal bone is replaced by a fibrous-like tissue with immature osteogenesis. Bone lesions are mono- or polyostotic and may be associated with bone pain and fragility, leading to fractures. In some patients or bone sites, they are hypertrophic, and responsible for neurological complications.

Revision as of 12:06, 13 August 2026

Fibrous dysplasia of bone is a congenital non-hereditary benign bone disease, where normal bone is replaced by a fibrous-like tissue with immature osteogenesis. Bone lesions are mono- or polyostotic and may be associated with bone pain and fragility, leading to fractures. In some patients or bone sites, they are hypertrophic, and responsible for neurological complications.
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    Fibrous dysplasia of bone
    Fibrous dysplasia of bone is a congenital non-hereditary benign bone disease, where normal bone is replaced by a fibrous-like tissue with immature osteogenesis. Bone lesions are mono- or polyostotic and may be associated with bone pain and fragility, leading to fractures. In some patients or bone sites, they are hypertrophic, and responsible for neurological complications.

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