Does osteofibrous dysplasia progress to adamantinoma and how should they be treated?
- PMID: 28249983
- DOI: 10.1302/0301-620X.99B3.38050
Does osteofibrous dysplasia progress to adamantinoma and how should they be treated?
Abstract
Aims: The aim of this study was to identify any progression between benign osteofibrous dysplasia (OFD), OFD-like adamantinoma and malignant adamantinoma, and to investigate the rates of local recurrence, metastases and survival, in order to develop treatment algorithms for each.
Patients and methods: A single institution retrospective review of all patients presenting with OFD, OFD-like adamantinoma and adamantinoma between 1973 and 2012 was undertaken. Complete data were available for 73 patients (42 with OFD; ten with an OFD-like adamantinoma and 21 with an adamantinoma). The mean follow-up was 10.3 years (3 to 25) for OFD, 9.2 years (3.0 to 26.3) for OFD-like and 11.6 years (0.25 to 33) for adamantinoma.
Results: The mean age at diagnosis for OFD was 13.5 years (1 to 49), 10.5 years (6 to 28) for OFD-like and 34 years (14 to 86) for adamantinoma. A total of 24 of the 42 patients with OFD (57%) have not required any treatment and have been managed with observation. A total of 18 of the 42 patients with OFD underwent surgery, 13 with curettage and five with resection. In all, three patients developed recurrence following curettage (23%) but none following resection. All these patients were cured with further limited surgery. A total of six patients initially diagnosed with OFD were subsequently found to have OFD-like adamantinoma. Of the ten patients initially diagnosed with OFD-like adamantinoma, three (30%) were managed with observation alone and seven underwent surgery, two with curettage and five with resection. Local recurrence arose in two patients, one each after curettage and resection. No patients with either OFD or an OFD-like adamantinoma developed metastases or had progression to adamantinoma. All patients with an adamantinoma were treated by surgery, three with curettage, six with amputation and 12 with excision. In all, two of the three treated with curettage developed local recurrence, requiring further surgery. Late development of both local recurrence and metastases led to a ten year disease specific survival of 93% which had dropped to 39% by 20 years.
Conclusion: We found no evidence of progression from OFD to adamantinoma. Conservative management with observation or curettage is often successful for patients with OFD and OFD-like adamantinoma. Resection with clear margins is required for patients with adamantinoma. Late tumour recurrence is not uncommon in adamantinoma and prolonged follow-up should be considered. Cite this article: Bone Joint J 2017;99-B:409-16.
Keywords: Adamantinoma; Osteofibrous dysplasia; Osteofibrous dysplasia -like adamantinoma.
©2017 The British Editorial Society of Bone & Joint Surgery.
Similar articles
-
Long-term outcome following treatment of Adamantinoma and Osteofibrous dysplasia of long bones.Orthop Traumatol Surg Res. 2016 Nov;102(7):925-932. doi: 10.1016/j.otsr.2016.08.010. Epub 2016 Oct 10. Orthop Traumatol Surg Res. 2016. PMID: 27745864
-
Osteofibrous dysplasia of the tibia : the importance of deformity in surveillance.Bone Joint J. 2022 Feb;104-B(2):302-308. doi: 10.1302/0301-620X.104B2.BJJ-2021-0815.R1. Bone Joint J. 2022. PMID: 35094574
-
Outcome of osteofibrous dysplasia-like versus classic adamantinoma of long bones: a single-institution experience.J Orthop Surg Res. 2020 Jul 16;15(1):268. doi: 10.1186/s13018-020-01769-5. J Orthop Surg Res. 2020. PMID: 32677983 Free PMC article.
-
A classic adamantinoma arising from osteofibrous dysplasia-like adamantinoma in the lower leg: a case report and review of the literature.Tohoku J Exp Med. 2006 May;209(1):53-9. doi: 10.1620/tjem.209.53. Tohoku J Exp Med. 2006. PMID: 16636523 Review.
-
Osteofibrous dysplasia and adamantinoma.J Am Acad Orthop Surg. 2010 Jun;18(6):358-66. doi: 10.5435/00124635-201006000-00008. J Am Acad Orthop Surg. 2010. PMID: 20511441 Review.
Cited by
-
Persistent Challenges: A Recurrent Adamantinoma - Case Report.J Orthop Case Rep. 2024 Jul;14(7):51-54. doi: 10.13107/jocr.2024.v14.i07.4572. J Orthop Case Rep. 2024. PMID: 39035399 Free PMC article.
-
Osteofibrous dysplasia-like adamantinoma treated via intercalary segmental resection with partial cortex preservation using pedicled vascularized fibula graft: a case report.World J Surg Oncol. 2020 Aug 13;18(1):203. doi: 10.1186/s12957-020-01983-9. World J Surg Oncol. 2020. PMID: 32792007 Free PMC article.
-
Adamantinoma of Pelvis: A Rare Tumor at an Uncommon Site, with Diagnostic Implications.Indian J Orthop. 2020 Jul 18;55(Suppl 1):261-266. doi: 10.1007/s43465-020-00196-2. eCollection 2021 May. Indian J Orthop. 2020. PMID: 34122777 Free PMC article.
-
TIBIAL ADAMANTINOMA: ANALYSIS OF SEVEN CONSECUTIVE CASES IN A SINGLE INSTITUTION.Acta Ortop Bras. 2018;26(4):252-254. doi: 10.1590/1413-785220182604192680. Acta Ortop Bras. 2018. PMID: 30210255 Free PMC article.
-
Osteofibrous dysplasia-like adamantinoma of isolated fibula in a child mimicking chronic osteomyelitis with pathological fracture.J Surg Case Rep. 2022 Jun 7;2022(6):rjac196. doi: 10.1093/jscr/rjac196. eCollection 2022 Jun. J Surg Case Rep. 2022. PMID: 35685295 Free PMC article.
MeSH terms
Supplementary concepts
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical