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Hereditary multiple exostoses with a giant osteochondroma degenerated into chondrosarcoma.
Masino, Federica; Montatore, Manuela; Carpentiere, Rossella; Balbino, Marina; Gifuni, Rossella; Fascia, Giacomo; Guglielmi, Giuseppe.
Afiliação
  • Masino F; Department of Clinical and Experimental Medicine, Foggia University School of Medicine, Viale L. Pinto 1, 71121, Foggia , Italy.
  • Montatore M; Department of Clinical and Experimental Medicine, Foggia University School of Medicine, Viale L. Pinto 1, 71121, Foggia , Italy.
  • Carpentiere R; Radiology Unit, "Dimiccoli" Hospital, Viale Ippocrate 15, 70051, Barletta, Italy.
  • Balbino M; Department of Clinical and Experimental Medicine, Foggia University School of Medicine, Viale L. Pinto 1, 71121, Foggia , Italy.
  • Gifuni R; Department of Clinical and Experimental Medicine, Foggia University School of Medicine, Viale L. Pinto 1, 71121, Foggia , Italy.
  • Fascia G; Department of Clinical and Experimental Medicine, Foggia University School of Medicine, Viale L. Pinto 1, 71121, Foggia , Italy.
  • Guglielmi G; Department of Clinical and Experimental Medicine, Foggia University School of Medicine, Viale L. Pinto 1, 71121, Foggia , Italy.
Radiol Case Rep ; 19(8): 2943-2949, 2024 Aug.
Article em En | MEDLINE | ID: mdl-38737181
ABSTRACT
We present a case of hereditary multiple exostoses with malignant transformation to chondrosarcoma in a woman complaining of enlargement and pain in the right thigh. Hereditary multiple exostoses is a rare genetic disorder characterized by multiple osteochondromas. Malignant transformation to chondrosarcoma of a pre-existing osteochondroma is a possible significant manifestation of this hereditary syndrome. Imaging modalities such as X-ray, Ultrasound, and computed tomography play a crucial role in the diagnosis and management of these patients, as described in this case.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Radiol Case Rep Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Itália

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Radiol Case Rep Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Itália
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