Polyostotic fibrous dysplasia. A long term follow up of 8 patients

Toshihumi Ozaki, M. Sugihara, Y. Nakatsuka, A. Kawai, H. Inoue

Research output: Contribution to journalArticle

30 Citations (Scopus)

Abstract

Eight patients who had polyostotic fibrous dysplasia were followed up for more than 10 years. One had the Albright syndrome. Two of 3 proximal femoral lesions which were treated before puberty by either curettage and bone grafting or by osteotomy, developed progressive deformity during the growth period. One of 2 proximal femoral lesions treated by curettage and bone grafting after the age of 18 also developed a deformity. Two tibial lesions operated on at the age of one and 30 years remained stable. The histological findings showed more active lesions in young patients compared with adults.

Original languageEnglish
Pages (from-to)227-232
Number of pages6
JournalInternational Orthopaedics
Volume20
Issue number4
DOIs
Publication statusPublished - 1996

Fingerprint

Polyostotic Fibrous Dysplasia
Curettage
Bone Transplantation
Thigh
Puberty
Osteotomy
Growth

ASJC Scopus subject areas

  • Surgery
  • Orthopedics and Sports Medicine

Cite this

Polyostotic fibrous dysplasia. A long term follow up of 8 patients. / Ozaki, Toshihumi; Sugihara, M.; Nakatsuka, Y.; Kawai, A.; Inoue, H.

In: International Orthopaedics, Vol. 20, No. 4, 1996, p. 227-232.

Research output: Contribution to journalArticle

Ozaki, Toshihumi ; Sugihara, M. ; Nakatsuka, Y. ; Kawai, A. ; Inoue, H. / Polyostotic fibrous dysplasia. A long term follow up of 8 patients. In: International Orthopaedics. 1996 ; Vol. 20, No. 4. pp. 227-232.
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