Literature DB >> 9768065

[Treatment of fibrous dysplasia of the cranio-facial bones. Report of 25 cases].

V Pinsolle1, J Rivel, V Michelet, C Majoufre, J Pinsolle.   

Abstract

Fibrous dysplasia accounts for approximately 2% of bone tumors. The ribs, proximal femurs and cranio-facial bones represent the majority of bone lesions. Surgery is the mainstay of treatment but the technique is controversial: conservative surgery or removal of dysplastic lesions followed by implantation of autogenous bone graft. The aim of this study was to assess the indications of each method. The medical records of 25 patients with fibrous dysplasia of the cranio-facial bones treated between January 1, 1980 and December 31, 1994 at the Department of Maxillofacial Surgery, Centre Hospitalier Universitaire de Bordeaux, France, were reviewed. Fourteen (56%) patients were women and 11 (44%) men. The median age at the time of diagnosis was 23 years (ranging from 8 to 56 years). The mean follow-up was 8 years. Two patients were unavailable for follow-up after treatment. The primary sites of the tumors were the mandible (n = 19 [76%]), maxilla (n = 1 [4%]) and skull (n = 5 [20%]). For mandibular lesions, the primary treatment always included a correction of deformations and asymmetry, which was the only treatment in 14 cases. Two patients required subsequent surgery to reduce further bone enlargement (1 and 2 years later in the first case and 11 years later in the second) without further problems. In 3 cases a segmental mandibulectomy followed by implantation of autogenous bone graft was required, and no further recurrence was observed. Therefore, the success rate of conservative surgery was 74% initially, and up to 86% after subsequent surgery. Skull lesions, although often very extensive, were remarkably stable and asymptomatic. They were successfully treated 4 times by conservative surgery, mainly for cosmetic reasons. One patient, with an ethmoidal tumor producing a mass effect along the course of the optic nerve, underwent a combined cranio-facial resection. As for the only maxillary tumor, three curettages were performed throughout an 11-year period and there was no evidence of further recurrence 4 years after the last intervention. In all cases, conservative surgery may be recommended as primary treatment of fibrous of the craniofacial bones, providing essential structures like the optic nerve are not at risk. Cosmetic results and local control proved excellent, and a further removal of the tumor remained feasible in the event of a recurrence. Success or failure did not correlate with tumor size, which justifies the use of this technique.

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Year:  1998        PMID: 9768065

Source DB:  PubMed          Journal:  Ann Chir Plast Esthet        ISSN: 0294-1260            Impact factor:   0.660


  5 in total

1.  Gene expression profiling of craniofacial fibrous dysplasia reveals ADAMTS2 overexpression as a potential marker.

Authors:  Shang-Hui Zhou; Wen-Jun Yang; Sheng-Wen Liu; Jiang Li; Chun-Ye Zhang; Yun Zhu; Chen-Ping Zhang
Journal:  Int J Clin Exp Pathol       Date:  2014-12-01

2.  Craniofacial Fibrous Dysplasia in an Elderly Patient: A Case Report with a Review of Literature.

Authors:  Suresh K Sachdeva
Journal:  Acta Stomatol Croat       Date:  2015-03

3.  Fibrous dysplasia of ethmoid - a rare presentation.

Authors:  Indra Nath Kundu; Saumitra Biswas
Journal:  Indian J Otolaryngol Head Neck Surg       Date:  2002-04

4.  CT and MR Imaging in a Large Series of Patients with Craniofacial Fibrous Dysplasia.

Authors:  Mehmet Haydar Atalar; Ismail Salk; Recep Savas; Ismail Onder Uysal; Hulusi Egilmez
Journal:  Pol J Radiol       Date:  2015-05-04

5.  Recurrent Monostotic Fibrous Dysplasia in the Mandible.

Authors:  Nilton Alves; Reinaldo José de Oliveira; Denise Takehana; Naira Figueiredo Deana
Journal:  Case Rep Dent       Date:  2016-05-31
  5 in total

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