Skip to main content
Top
Published in: Skeletal Radiology 1/2020

01-01-2020 | Chondrosarcoma | Scientific Article

Whole-body MRI in assessing malignant transformation in multiple hereditary exostoses and enchondromatosis: audit results and literature review

Authors: Anne Grethe Jurik, Peter Holmberg Jørgensen, Mikkel Meng Mortensen

Published in: Skeletal Radiology | Issue 1/2020

Login to get access

Abstract

Objective

To analyze the results of annual screening using whole-body magnetic resonance imaging (WBMRI) in patients with multiple hereditary exostoses (MHE) and enchondromatosis (EC), and estimate the risk for transformation to chondrosarcoma (CS) in these disorders.

Materials and methods

A total of 62 patients (57 with MHE and five with EC) screened during a mean follow-up period of 4.6 years (range, 1–10 years) using 253 WBMRIs (median four WBMRIs per patient, range, 1–10) were analyzed retrospectively. The time of WBMRIs was compared with dates for diagnosed CSs. A supplementary literature review was performed focusing on the risk of malignant transformation.

Results

Ten patients had CS before being enrolled in the screening program, nine with MHE and one with EC. Three asymptomatic CSs were detected by screening; one in a patient with EC and two in patients with MHE, one of whom had CS previously. During the screening period, there was no occurrence of CS not detected by WBMRI in the study group.
Histopathologically, the CSs were predominantly grade 1 and were, except for in two patients, located at the truncus, proximal femur, and shoulder girdle.
Based on the current material and literature review, the risk of CS seems to be in the range of 2–3.7% for MHE and up to 50% for EC patients.

Conclusions

MRI may be used as a screening method detecting malignant transformation in MHE and EC patients, but the efficacy has to be confirmed in long-term follow-up studies including cost analysis.
Literature
1.
go back to reference Altay M, Bayrakci K, Yildiz Y, Erekul S, Saglik Y. Secondary chondrosarcoma in cartilage bone tumors: report of 32 patients. J Orthop Sci. 2007;12(5):415–23.CrossRef Altay M, Bayrakci K, Yildiz Y, Erekul S, Saglik Y. Secondary chondrosarcoma in cartilage bone tumors: report of 32 patients. J Orthop Sci. 2007;12(5):415–23.CrossRef
2.
go back to reference Black B, Dooley J, Pyper A, Reed M. Multiple hereditary exostoses. An epidemiologic study of an isolated community in Manitoba. Clin Orthop Relat Res. 1993;287(287):212–7. Black B, Dooley J, Pyper A, Reed M. Multiple hereditary exostoses. An epidemiologic study of an isolated community in Manitoba. Clin Orthop Relat Res. 1993;287(287):212–7.
3.
go back to reference Brien EW, Mirra JM, Luck JV. Jr. benign and malignant cartilage tumors of bone and joint: their anatomic and theoretical basis with an emphasis on radiology, pathology and clinical biology. II. Juxtacortical cartilage tumors. Skelet Radiol. 1999;28(1):1–20.CrossRef Brien EW, Mirra JM, Luck JV. Jr. benign and malignant cartilage tumors of bone and joint: their anatomic and theoretical basis with an emphasis on radiology, pathology and clinical biology. II. Juxtacortical cartilage tumors. Skelet Radiol. 1999;28(1):1–20.CrossRef
4.
go back to reference Clement ND, Ng CE, Porter DE. Shoulder exostoses in hereditary multiple exostoses: probability of surgery and malignant change. J Shoulder Elb Surg. 2011;20(2):290–4.CrossRef Clement ND, Ng CE, Porter DE. Shoulder exostoses in hereditary multiple exostoses: probability of surgery and malignant change. J Shoulder Elb Surg. 2011;20(2):290–4.CrossRef
5.
go back to reference Czajka CM, DiCaprio MR. What is the proportion of patients with multiple hereditary exostoses who undergo malignant degeneration? Clin Orthop Relat Res. 2015;473(7):2355–61.CrossRef Czajka CM, DiCaprio MR. What is the proportion of patients with multiple hereditary exostoses who undergo malignant degeneration? Clin Orthop Relat Res. 2015;473(7):2355–61.CrossRef
6.
go back to reference Gordon SL, Buchanan JR, Ladda RL. Hereditary multiple exostoses: report of a kindred. J Med Genet. 1981;18(6):428–30.CrossRef Gordon SL, Buchanan JR, Ladda RL. Hereditary multiple exostoses: report of a kindred. J Med Genet. 1981;18(6):428–30.CrossRef
7.
go back to reference Crandall BF, Field LL, Sparkes RS, Spence MA. Hereditary multiple exostoses. Report of a family. Clin Orthop Relat Res. 1984;190(190):217–9. Crandall BF, Field LL, Sparkes RS, Spence MA. Hereditary multiple exostoses. Report of a family. Clin Orthop Relat Res. 1984;190(190):217–9.
8.
go back to reference Goud AL, de Lange J, Scholtes VA, Bulstra SK, Ham SJ. Pain, physical and social functioning, and quality of life in individuals with multiple hereditary exostoses in the Netherlands: a national cohort study. J Bone Joint Surg Am. 2012;94(11):1013–20.CrossRef Goud AL, de Lange J, Scholtes VA, Bulstra SK, Ham SJ. Pain, physical and social functioning, and quality of life in individuals with multiple hereditary exostoses in the Netherlands: a national cohort study. J Bone Joint Surg Am. 2012;94(11):1013–20.CrossRef
9.
go back to reference Kivioja A, Ervasti H, Kinnunen J, Kaitila I, Wolf M, Bohling T. Chondrosarcoma in a family with multiple hereditary exostoses. J Bone Joint Surg Br. 2000;82(2):261–6.CrossRef Kivioja A, Ervasti H, Kinnunen J, Kaitila I, Wolf M, Bohling T. Chondrosarcoma in a family with multiple hereditary exostoses. J Bone Joint Surg Br. 2000;82(2):261–6.CrossRef
10.
go back to reference Francannet C, Cohen-Tanugi A, Le Merrer M, Munnich A, Bonaventure J, Legeai-Mallet L. Genotype-phenotype correlation in hereditary multiple exostoses. J Med Genet. 2001;38(7):430–4.CrossRef Francannet C, Cohen-Tanugi A, Le Merrer M, Munnich A, Bonaventure J, Legeai-Mallet L. Genotype-phenotype correlation in hereditary multiple exostoses. J Med Genet. 2001;38(7):430–4.CrossRef
11.
go back to reference Pedrini E, Jennes I, Tremosini M, et al. Genotype-phenotype correlation study in 529 patients with multiple hereditary exostoses: identification of "protective" and "risk" factors. J Bone Joint Surg Am. 2011;93(24):2294–302.CrossRef Pedrini E, Jennes I, Tremosini M, et al. Genotype-phenotype correlation study in 529 patients with multiple hereditary exostoses: identification of "protective" and "risk" factors. J Bone Joint Surg Am. 2011;93(24):2294–302.CrossRef
12.
go back to reference Pierz KA, Stieber JR, Kusumi K, Dormans JP. Hereditary multiple exostoses: one center’s experience and review of etiology. Clin Orthop Relat Res. 2002;401(401):49–59.CrossRef Pierz KA, Stieber JR, Kusumi K, Dormans JP. Hereditary multiple exostoses: one center’s experience and review of etiology. Clin Orthop Relat Res. 2002;401(401):49–59.CrossRef
13.
go back to reference Porter DE, Lonie L, Fraser M, et al. Severity of disease and risk of malignant change in hereditary multiple exostoses. A genotype-phenotype study. J Bone Joint Surg Br. 2004;86(7):1041–6.CrossRef Porter DE, Lonie L, Fraser M, et al. Severity of disease and risk of malignant change in hereditary multiple exostoses. A genotype-phenotype study. J Bone Joint Surg Br. 2004;86(7):1041–6.CrossRef
14.
go back to reference Schmale GA, Conrad EU 3rd, Raskind WH. The natural history of hereditary multiple exostoses. J Bone Joint Surg Am. 1994;76(7):986–92.CrossRef Schmale GA, Conrad EU 3rd, Raskind WH. The natural history of hereditary multiple exostoses. J Bone Joint Surg Am. 1994;76(7):986–92.CrossRef
15.
go back to reference Wicklund CL, Pauli RM, Johnston D, Hecht JT. Natural history study of hereditary multiple exostoses. Am J Med Genet. 1995;55(1):43–6.CrossRef Wicklund CL, Pauli RM, Johnston D, Hecht JT. Natural history study of hereditary multiple exostoses. Am J Med Genet. 1995;55(1):43–6.CrossRef
16.
go back to reference Vanhoenacker FM, Van Hul W, Wuyts W, Willems PJ, De Schepper AM. Hereditary multiple exostoses: from genetics to clinical syndrome and complications. Eur J Radiol. 2001;40(3):208–17.CrossRef Vanhoenacker FM, Van Hul W, Wuyts W, Willems PJ, De Schepper AM. Hereditary multiple exostoses: from genetics to clinical syndrome and complications. Eur J Radiol. 2001;40(3):208–17.CrossRef
17.
go back to reference Tong K, Liu H, Wang X, et al. Osteochondroma: review of 431 patients from one medical institution in South China. J Bone Oncol. 2017;8:23–9.CrossRef Tong K, Liu H, Wang X, et al. Osteochondroma: review of 431 patients from one medical institution in South China. J Bone Oncol. 2017;8:23–9.CrossRef
18.
go back to reference Voutsinas S, Wynne-Davies R. The infrequency of malignant disease in diaphyseal aclasis and neurofibromatosis. J Med Genet. 1983;20(5):345–9.CrossRef Voutsinas S, Wynne-Davies R. The infrequency of malignant disease in diaphyseal aclasis and neurofibromatosis. J Med Genet. 1983;20(5):345–9.CrossRef
19.
go back to reference Liu J, Hudkins PG, Swee RG, Unni KK. Bone sarcomas associated with Ollier’s disease. Cancer. 1987;59(7):1376–85.CrossRef Liu J, Hudkins PG, Swee RG, Unni KK. Bone sarcomas associated with Ollier’s disease. Cancer. 1987;59(7):1376–85.CrossRef
20.
go back to reference Brien EW, Mirra JM, Kerr R. Benign and malignant cartilage tumors of bone and joint: their anatomic and theoretical basis with an emphasis on radiology, pathology and clinical biology. I The intramedullary cartilage tumors. Skeletal Radiol. 1997;26(6):325–53.CrossRef Brien EW, Mirra JM, Kerr R. Benign and malignant cartilage tumors of bone and joint: their anatomic and theoretical basis with an emphasis on radiology, pathology and clinical biology. I The intramedullary cartilage tumors. Skeletal Radiol. 1997;26(6):325–53.CrossRef
21.
go back to reference Verdegaal SH, Bovee JV, Pansuriya TC, et al. Incidence, predictive factors, and prognosis of chondrosarcoma in patients with Ollier disease and Maffucci syndrome: an international multicenter study of 161 patients. Oncologist. 2011;16(12):1771–9.CrossRef Verdegaal SH, Bovee JV, Pansuriya TC, et al. Incidence, predictive factors, and prognosis of chondrosarcoma in patients with Ollier disease and Maffucci syndrome: an international multicenter study of 161 patients. Oncologist. 2011;16(12):1771–9.CrossRef
22.
go back to reference Hameetman L, Bovee JV, Taminiau AH, Kroon HM, Hogendoorn PC. Multiple osteochondromas: clinicopathological and genetic spectrum and suggestions for clinical management. Hered Cancer Clin Pract. 2004;2(4):161–73.CrossRef Hameetman L, Bovee JV, Taminiau AH, Kroon HM, Hogendoorn PC. Multiple osteochondromas: clinicopathological and genetic spectrum and suggestions for clinical management. Hered Cancer Clin Pract. 2004;2(4):161–73.CrossRef
23.
go back to reference Gariani J, Westerland O, Natas S, Verma H, Cook G, Goh V. Comparison of whole-body magnetic resonance imaging (WBMRI) to whole-body computed tomography (WBCT) or (18)F-fluorodeoxyglucose positron emission tomography/CT ((18)F-FDG PET/CT) in patients with myeloma: systematic review of diagnostic performance. Crit Rev Oncol Hematol. 2018;124:66–72.CrossRef Gariani J, Westerland O, Natas S, Verma H, Cook G, Goh V. Comparison of whole-body magnetic resonance imaging (WBMRI) to whole-body computed tomography (WBCT) or (18)F-fluorodeoxyglucose positron emission tomography/CT ((18)F-FDG PET/CT) in patients with myeloma: systematic review of diagnostic performance. Crit Rev Oncol Hematol. 2018;124:66–72.CrossRef
24.
go back to reference Sampath Kumar V, Tyrrell PN, Singh J, Gregory J, Cribb GL, Cool P. Surveillance of intramedullary cartilage tumours in long bones. Bone Joint J. 2016;98-B(11):1542–7.CrossRef Sampath Kumar V, Tyrrell PN, Singh J, Gregory J, Cribb GL, Cool P. Surveillance of intramedullary cartilage tumours in long bones. Bone Joint J. 2016;98-B(11):1542–7.CrossRef
25.
go back to reference Anupindi SA, Bedoya MA, Lindell RB, et al. Diagnostic performance of whole-body MRI as a tool for Cancer screening in children with genetic Cancer-predisposing conditions. AJR Am J Roentgenol. 2015;205(2):400–8.CrossRef Anupindi SA, Bedoya MA, Lindell RB, et al. Diagnostic performance of whole-body MRI as a tool for Cancer screening in children with genetic Cancer-predisposing conditions. AJR Am J Roentgenol. 2015;205(2):400–8.CrossRef
26.
go back to reference Greer MC, Voss SD, States LJ. Pediatric cancer predisposition imaging: focus on whole-body MRI. Clin Cancer Res. 2017;23(11):e6–e13.CrossRef Greer MC, Voss SD, States LJ. Pediatric cancer predisposition imaging: focus on whole-body MRI. Clin Cancer Res. 2017;23(11):e6–e13.CrossRef
27.
go back to reference Saya S, Killick E, Thomas S, Taylor N, Bancroft EK, Rothwell J, et al. Baseline results from the UK SIGNIFY study: a whole-body MRI screening study in TP53 mutation carriers and matched controls. Familial Cancer. 2017;16(3):433–40.CrossRef Saya S, Killick E, Thomas S, Taylor N, Bancroft EK, Rothwell J, et al. Baseline results from the UK SIGNIFY study: a whole-body MRI screening study in TP53 mutation carriers and matched controls. Familial Cancer. 2017;16(3):433–40.CrossRef
28.
go back to reference Bernard SA, Murphey MD, Flemming DJ, Kransdorf MJ. Improved differentiation of benign osteochondromas from secondary chondrosarcomas with standardized measurement of cartilage cap at CT and MR imaging. Radiology. 2010;255(3):857–65.CrossRef Bernard SA, Murphey MD, Flemming DJ, Kransdorf MJ. Improved differentiation of benign osteochondromas from secondary chondrosarcomas with standardized measurement of cartilage cap at CT and MR imaging. Radiology. 2010;255(3):857–65.CrossRef
29.
go back to reference Ahmed AR, Tan TS, Unni KK, Collins MS, Wenger DE, Sim FH. Secondary chondrosarcoma in osteochondroma: report of 107 patients. Clin Orthop Relat Res. 2003;(411):193–206 doi(411):193–206.CrossRef Ahmed AR, Tan TS, Unni KK, Collins MS, Wenger DE, Sim FH. Secondary chondrosarcoma in osteochondroma: report of 107 patients. Clin Orthop Relat Res. 2003;(411):193–206 doi(411):193–206.CrossRef
30.
go back to reference Sonne-Holm E, Wong C, Sonne-Holm S. Multiple cartilaginous exostoses and development of chondrosarcomas—a systematic review. Dan Med J. 2014;61(9):A4895.PubMed Sonne-Holm E, Wong C, Sonne-Holm S. Multiple cartilaginous exostoses and development of chondrosarcomas—a systematic review. Dan Med J. 2014;61(9):A4895.PubMed
31.
go back to reference Pansuriya TC, Kroon HM, Bovee JV. Enchondromatosis: insights on the different subtypes. Int J Clin Exp Pathol. 2010;3(6):557–69.PubMedPubMedCentral Pansuriya TC, Kroon HM, Bovee JV. Enchondromatosis: insights on the different subtypes. Int J Clin Exp Pathol. 2010;3(6):557–69.PubMedPubMedCentral
32.
go back to reference Wuisman PI, Jutte PC, Ozaki T. Secondary chondrosarcoma in osteochondromas. Medullary extension in 15 of 45 cases. Acta Orthop Scand. 1997;68(4):396–400.CrossRef Wuisman PI, Jutte PC, Ozaki T. Secondary chondrosarcoma in osteochondromas. Medullary extension in 15 of 45 cases. Acta Orthop Scand. 1997;68(4):396–400.CrossRef
33.
go back to reference Goud AL, Wuyts W, Bessems J, Bramer J, van der Woude HJ, Ham J. Intraosseous atypical chondroid tumor or chondrosarcoma grade 1 in patients with multiple osteochondromas. J Bone Joint Surg Am. 2015;97(1):24–31.CrossRef Goud AL, Wuyts W, Bessems J, Bramer J, van der Woude HJ, Ham J. Intraosseous atypical chondroid tumor or chondrosarcoma grade 1 in patients with multiple osteochondromas. J Bone Joint Surg Am. 2015;97(1):24–31.CrossRef
34.
go back to reference Hendel HW, Daugaard S, Kjaer A. Utility of planar bone scintigraphy to distinguish benign osteochondromas from malignant chondrosarcomas. Clin Nucl Med. 2002;27(9):622–4.CrossRef Hendel HW, Daugaard S, Kjaer A. Utility of planar bone scintigraphy to distinguish benign osteochondromas from malignant chondrosarcomas. Clin Nucl Med. 2002;27(9):622–4.CrossRef
35.
go back to reference Subhawong TK, Winn A, Shemesh SS, Pretell-Mazzini J. F-18 FDG PET differentiation of benign from malignant chondroid neoplasms: a systematic review of the literature. Skelet Radiol. 2017;46(9):1233–9.CrossRef Subhawong TK, Winn A, Shemesh SS, Pretell-Mazzini J. F-18 FDG PET differentiation of benign from malignant chondroid neoplasms: a systematic review of the literature. Skelet Radiol. 2017;46(9):1233–9.CrossRef
36.
go back to reference Staal HM, Dremmen MHG, Robben SGF, Witlox AMA, Rhijn LW. The use of whole-body MR imaging in children with HMO, an extended case study in two patients. Pediatr Ther. 2016;6:275.CrossRef Staal HM, Dremmen MHG, Robben SGF, Witlox AMA, Rhijn LW. The use of whole-body MR imaging in children with HMO, an extended case study in two patients. Pediatr Ther. 2016;6:275.CrossRef
37.
go back to reference Doyle LA. Sarcoma classification: an update based on the 2013 World Health Organization classification of tumors of soft tissue and bone. Cancer. 2014;120:1763–74.CrossRef Doyle LA. Sarcoma classification: an update based on the 2013 World Health Organization classification of tumors of soft tissue and bone. Cancer. 2014;120:1763–74.CrossRef
38.
go back to reference The Skeletal Lesions Interobserver Correlation among Expert Diagnosticians (SLICED) Study Group. Reliability of histopathologic and radiologic grading of cartilaginous neoplasms in long bones. J Bone Joint Surg Am. 2007;89:2113–23.CrossRef The Skeletal Lesions Interobserver Correlation among Expert Diagnosticians (SLICED) Study Group. Reliability of histopathologic and radiologic grading of cartilaginous neoplasms in long bones. J Bone Joint Surg Am. 2007;89:2113–23.CrossRef
Metadata
Title
Whole-body MRI in assessing malignant transformation in multiple hereditary exostoses and enchondromatosis: audit results and literature review
Authors
Anne Grethe Jurik
Peter Holmberg Jørgensen
Mikkel Meng Mortensen
Publication date
01-01-2020
Publisher
Springer Berlin Heidelberg
Keyword
Chondrosarcoma
Published in
Skeletal Radiology / Issue 1/2020
Print ISSN: 0364-2348
Electronic ISSN: 1432-2161
DOI
https://doi.org/10.1007/s00256-019-03268-z

Other articles of this Issue 1/2020

Skeletal Radiology 1/2020 Go to the issue

Browser's Notes

Browser’s Notes