Ollier disease: A case report and literature review.
Enchondromatosis
Metaphyseal osteolytic lesion
Ollier disease
Journal
Radiology case reports
ISSN: 1930-0433
Titre abrégé: Radiol Case Rep
Pays: Netherlands
ID NLM: 101467888
Informations de publication
Date de publication:
Oct 2023
Oct 2023
Historique:
received:
22
05
2023
revised:
05
07
2023
accepted:
18
07
2023
medline:
18
8
2023
pubmed:
18
8
2023
entrez:
18
8
2023
Statut:
epublish
Résumé
Ollier disease is an uncommon disease characterized by several enchondromas and an asymmetric distribution of cartilage lesions, which can vary significantly in size, location, age, and gender. The primary symptom of this condition is a nonossifying chondrocyte mass or hamartomatous chondrocyte growth in the metaphysis of a short or long bone. Specific cases can progress to chondrosarcoma or osteosarcoma. X-ray is the most fundamental diagnostic technique for skeletal illnesses. In this article, we present a case of Ollier disease from Mother and Child Hospital IBN SINA, Rabat, Morocco.
Identifiants
pubmed: 37593331
doi: 10.1016/j.radcr.2023.07.042
pii: S1930-0433(23)00480-6
pmc: PMC10432136
doi:
Types de publication
Case Reports
Langues
eng
Pagination
3652-3656Informations de copyright
© 2023 The Authors. Published by Elsevier Inc. on behalf of University of Washington.
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