Osteofibröse dysplasie und ihre differentialdiagnose

Translated title of the contribution: Osteofibrous dysplasia and its differential diagnosis

F. Del Grande, G. U. Exner, J. Hodler

Research output: Contribution to journalArticlepeer-review


We present a case of a 13 year old girl with swelling and pain of the right lower leg persisting for four months. The radiological and histological diagnosis is osteofibrous dysplasia. Osteofibrous dysplasia is a rare bone lesion predominantly affecting the cortex of the tibia. Almost all patients are younger than ten years at presentation. Swelling is a typical clinical manifestation. Radiologically and even histologically the distinction between the osteofibrous dysplasia and the more aggressive adamantinoma can be difficult. Other bone lesions potentially mimicking osteofibrous dysplasia include: fibrous dysplasia, osteoid osteoma, osteosarcoma, osteoblastoma and intracortical Brodie's abcess. The natural course of the disease is unpredictible. Lesions with typical radiological appearance are considered to be «no touch lesions». In equivocal cases block resection (with both a diagnostic and therapeutic purpose) should be performed.

Translated title of the contributionOsteofibrous dysplasia and its differential diagnosis
Original languageGerman
Pages (from-to)1770-1774
Number of pages5
Issue number43
StatePublished - Oct 20 1999
Externally publishedYes


  • Adamantinoma
  • Bone tumors
  • Osteofibrous dysplasia
  • Radiology
  • Tibia
  • Tumors

ASJC Scopus subject areas

  • Medicine(all)


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