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Abstract
Surface tumors of the bone are broadly defined as a diverse group of osteogenic and chondrogenic benign and malignant neoplasms that arise adjacent to the outer surface of cortical bone. They may be a cause of diagnostic difficulty due to a degree of histological overlap, rarity, and nomenclature. In this review we summarize the different histological types of primary malignant tumors of bone surface, namely, secondary peripheral chondrosarcoma, periosteal chondrosarcoma, parosteal osteosarcoma, dedifferentiated parosteal osteosarcoma, periosteal osteosarcoma, and high-grade surface osteosarcoma. We provide a comprehensive updated review of their pathogenesis and highlight radiological, macroscopic, and histopathological features and recently available ancillary diagnostic tools that may aid in the differential diagnosis.
Keywords
Secondary peripheral chondrosarcoma
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periosteal chondrosarcoma
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parosteal osteosarcoma
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periosteal osteosarcoma
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high-grade surface osteosarcoma
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Marina Pacheco, Alberto Righi.
Primary malignant tumors of bone surface: a review with emphasis in differential diagnosis.
Journal of Cancer Metastasis and Treatment, 2020, 6: 49 DOI:10.20517/2394-4722.2020.85
| [1] |
Picci P,Donati DM.Diagnosis of musculoskeletal tumors and tumor-like conditions2020;2nd editionSwitzerlandSpringer Nature
|
| [2] |
Bovée JVMG,Flanagan AM.WHO Classification of Tumours of Soft Tissue and Bone.2020;5th editionLyonInternational Agency for research on cancer
|
| [3] |
Unni KK,Bridge JA,Wold LE.AFIP atlas of tumor pathology. Tumors of the bones and joints. 4th series.2005;Washington, DCThe American Registry of Pathology
|
| [4] |
Ahmed AR,Unni KK,Wenger DE.Secondary chondrosarcoma in osteochondroma: report of 107 patients..Clin Orthop Relat Res2003;193-206
|
| [5] |
Jones KB,Searby C.A mouse model of osteochondromagenesis from clonal inactivation of Ext1 in chondrocytes..Proc Natl Acad Sci U S A2010;107:2054-9 PMCID:PMC2836675
|
| [6] |
de Andrea CE,Prins F,Romeo S.Primary cilia organization reflects polarity in the growth plate and implies loss of polarity and mosaicism in osteochondroma..Lab Invest2010;90:1091-101
|
| [7] |
Matsumoto K,Mackem S.A mouse model of chondrocyte-specific somatic mutation reveals a role for Ext1 loss of heterozygosity in multiple hereditary exostoses..Proc Natl Acad Sci U S A2010;107:10932-7 PMCID:PMC2890731
|
| [8] |
Jennes I,Zuntini M.Multiple osteochondromas: mutation update and description of the multiple osteochondromas mutation database (MOdb)..Hum Mutat2009;30:1620-7
|
| [9] |
de Andrea CE,Kroon HM.Secondary peripheral chondrosarcoma evolving from osteochondroma as a result of outgrowth of cells with functional EXT..Oncogene2012;31:1095-104
|
| [10] |
Häcker U,Perrimon N.Heparan sulphate proteoglycans: the sweet side of development..Nat Rev Mol Cell Biol2005;6:530-41
|
| [11] |
Pacifici M.The pathogenic roles of heparan sulfate deficiency in hereditary multiple exostoses..Matrix Biol2018;71-72:28-39 PMCID:PMC6015767
|
| [12] |
Hallor KH,Bovée JV.Genomic profiling of chondrosarcoma: chromosomal patterns in central and peripheral tumors..Clin Cancer Res2009;15:2685-94
|
| [13] |
de Andrea CE.Epiphyseal growth plate and secondary peripheral chondrosarcoma: the neighbours matter..J Pathol2012;226:219-28
|
| [14] |
de Andrea CE,Jin H,Jones KB.Cell cycle deregulation and mosaic loss of Ext1 drive peripheral chondrosarcomagenesis in the mouse and reveal an intrinsic cilia deficiency..J Pathol2015;236:210-8 PMCID:PMC4564123
|
| [15] |
Nielsen GP,Deshpande V,Kattapuram SV.Diagnostic Pathology: Bone.2017;2nd ed.Philadelphia, PAElsevier
|
| [16] |
Vanel D,Monti C,Picci P.Radiological features of 24 periosteal chondrosarcomas..Skeletal Radiol2001;30:208-12
|
| [17] |
Amary MF,Maggiani F.IDH1 and IDH2 mutations are frequent events in central chondrosarcoma and central and periosteal chondromas but not in other mesenchymal tumours..J Pathol2011;224:334-43
|
| [18] |
Gelderblom H,Dijkstra SD.The clinical approach towards chondrosarcoma..Oncologist2008;13:320-29
|
| [19] |
van Maldegem AM,Palmerini E.Outcome of advanced, unresectable conventional central chondrosarcoma..Cancer2014;120:3159-64
|
| [20] |
Papagelopoulos PJ,Mavrogenis AF.Survivorship analysis in patients with periosteal chondrosarcoma..Clin OrthopRelat Res2006;448:199-207
|
| [21] |
Bertoni F,Laus M.Periosteal chondrosarcoma and periosteal osteosarcoma. Two distinct entities..J Bone Joint Surg Br1982;64:370-6
|
| [22] |
Cleven AH,Hogendoorn PC.Periosteal chondrosarcoma: a histopathological and molecular analysis of a rare chondrosarcoma subtype..Histopathology2015;67:483-90
|
| [23] |
Pansuriya TC,d’Adamo P.Somatic mosaic IDH1 and IDH2 mutations are associated with enchondroma and spindle cell hemangioma in Ollier disease and Maffucci syndrome..Nat Genet2011;43:1256-61 PMCID:PMC3427908
|
| [24] |
Dang L,Gross S.Cancer-associated IDH1 mutations produce 2-hydroxyglutarate..Nature2009;462:739-44 PMCID:PMC2818760
|
| [25] |
Suijker J,Roelofs H,Bovée JV.The oncometabolite D-2-hydroxyglutarate induced by mutant IDH1 or -2 blocks osteoblast differentiation in vitro and in vivo..Oncotarget2015;6:14832-42 PMCID:PMC4558118
|
| [26] |
Jin Y,Watanabe M.Mutant IDH1 dysregulates the differentiation of mesenchymal stem cells in association with gene-specific histone modifications to cartilage- and bone-related genes..PLoS One2015;10:e0131998 PMCID:PMC4498635
|
| [27] |
Czerniak B.Dorfman and Czerniak’s Bone Tumors.2016;2nd editionPhiladelphiaSaunders
|
| [28] |
Goedhart LM,Kroon HM,Jutte PC.The presentation, treatment and outcome of periosteal chondrosarcoma in the Netherlands..Bone Joint J2014;96:823-8
|
| [29] |
Ruengwanichayakun P,Frisoni T.Parosteal osteosarcoma: a monocentric retrospective analysis of 195 patients..Hum Pathol2019;91:11-8
|
| [30] |
Bertoni F,Staals EL.Dedifferentiated parosteal osteosarcoma: the experience of the Rizzoli Institute..Cancer2005;10:2373-82
|
| [31] |
Aparisi Gómez MP,Errani C.Inflammation and infiltration: can the radiologist draw a line? MRI versus CT to accurately assess medullary involvement in parosteal osteosarcoma..Int J Biol Markers2020;35:31-6
|
| [32] |
Reith JD,Hornicek FJ.Dedifferentiated parosteal osteosarcoma with rhabdomyosarcomatous differentiation..Skeletal Radiol1999;28:527-31
|
| [33] |
Szymanska J,Mertens F.Ring chromosomes in parosteal osteosarcoma contain sequences from 12q13-15: a combined cytogenetic and comparative genomic hybridization study..Genes Chromosomes Cancer1996;16:31-4
|
| [34] |
Dujardin F,Bouvier C.MDM2 and CDK4 immunohistochemistry is a valuable tool in the differential diagnosis of low-grade osteosarcomas and other primary fibro-osseous lesions of the bone..Mod Pathol2011;24:624-37
|
| [35] |
Duhamel LA,Halai D.Frequency of Mouse Double Minute 2 (MDM2) and Mouse Double Minute 4 (MDM4) amplification in parosteal and conventional osteosarcoma subtypes..Histopathology2012;60:357-9
|
| [36] |
Baumhoer D,Flanagan AM.An update of molecular pathology of bone tumors. Lessons learned from investigating samples by next generation sequencing..Genes Chromosomes Cancer2019;58:88-99
|
| [37] |
Bekers EM,Grünberg K.Myositis ossificans - another condition with USP6 rearrangement, providing evidence of a relationship with nodular fasciitis and aneurysmal bone cyst..Ann Diagn Pathol.2018;34:56-9
|
| [38] |
Meneses MF,Swee RG.Bizarre parostealosteochondromatous proliferation of bone (Nora’s lesion)..Am J Surg Pathol1993;17:691-7
|
| [39] |
Berber O,Jalgaonkar A.Bizarre parostealosteochondromatous proliferation of bone: clinical management of a series of 22 cases..J Bone Joint Surg Br2011;93:1118-21
|
| [40] |
Abramovici L.Bizarre parostealosteochondromatous proliferation (Nora’s lesion): a retrospective study of 12 cases, 2 arising in long bones..Hum Pathol2002;3:1205-10
|
| [41] |
Lewis VO,Springfield DS.Parosteal osteosarcoma of the posterior aspect of the distal part of the femur. Oncological and functional results following a new resection technique..J Bone Joint Surg Am2000;82:1083-8
|
| [42] |
Han I,Na YG,Kim HS.Clinical outcome of parosteal osteosarcoma..J Surg Oncol2008;97:146-9
|
| [43] |
Laitinen M,Albergo JI.The prognostic and therapeutic factors which influence the oncological outcome of parosteal osteosarcoma..Bone Joint J2015;97:1698-703
|
| [44] |
Cesari M,Vanel D.Periosteal osteosarcoma: a single-institution experience..Cancer.2011;117:1731-5
|
| [45] |
Chan CM,Spiguel ARV,Scarborough MT.Periosteal Osteosarcoma: a single-institutional study of factors related to oncologic outcomes..Sarcoma.2018;2018:8631237 PMCID:PMC6180962
|
| [46] |
Grimer RJ,Flege S.Periosteal osteosarcoma:a European review of outcome..Eur J Cancer2005;41:2806-11
|
| [47] |
Righi A,Benini S.MDM2 and CDK4 expression in periosteal osteosarcoma..Hum Pathol2015;46:549-53
|
| [48] |
Ritts GD,Unni KK,Eckardt JJ.Periosteal osteosarcoma..Clin Orthop Relat Res1987;219:299-307
|
| [49] |
Okada K,Swee RG.High grade surface osteosarcoma: a clinicopathologic study of 46 cases..Cancer1999;85:1044-54
|
| [50] |
Staals EL,Bertoni F.High-grade surface osteosarcoma: a review of 25 cases from the Rizzoli Institute..Cancer2008;112:1592-9
|