Zobrazeno 1 - 10
of 32
pro vyhledávání: '"Secondary Peripheral Chondrosarcoma"'
Autor:
Maria Gnoli, Marco Gambarotti, Alberto Righi, Eric Lodewijk Staals, Andrea Evangelista, Morena Tremosini, Evelise Brizola, Marina Mordenti, Manila Boarini, Manuela Locatelli, Elena Pedrini, Luca Sangiorgi
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 19, Iss 1, Pp 1-10 (2024)
Abstract Background Multiple osteochondromas is genetic disorder characterized by the formation of multiple benign cartilage-capped bone tumors, named osteochondromas, during skeletal development. The most feared complication is the secondary periphe
Externí odkaz:
https://doaj.org/article/39630631ea254982b0c1ea691e0ae7c2
Akademický článek
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Autor:
Alberto Righi, Marina Pacheco, Stefania Cocchi, Sofia Asioli, Marco Gambarotti, Davide Maria Donati, Andrea Evangelista, Maria Gnoli, Manuela Locatelli, Marina Mordenti, Manila Boarini, Evelise Brizola, Elena Pedrini, Luca Sangiorgi
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 17, Iss 1, Pp 1-8 (2022)
Abstract Background Secondary peripheral chondrosarcomas arising in solitary osteochondromas is an unusual complication, reported in small series. In this study, we aimed to present our experience with this rare variant of chondrosarcoma and compare
Externí odkaz:
https://doaj.org/article/45965d4def734b6fb07d33073a0c9492
Autor:
Arjen H.G. Cleven, Judith V.M.G. Bovée
Publikováno v:
Diagnostic Histopathology. 26:484-491
Chondrogenic or cartilaginous tumours represent the most common bone tumours and can be diagnostically challenging especially on scarce biopsy material. As morphologically they may overlap, correlation between radiological and pathological findings a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2996944e5c16dd7b05ca182de2e6ed56
https://doi.org/10.1016/j.mpdhp.2020.07.006
https://doi.org/10.1016/j.mpdhp.2020.07.006
Autor:
Divya Joshi, Teerthanath Srinivas, Aditya H. Kumar, Shubha P. Bhat, Siddharth M. Shetty, Vinay Kumar J. Rajendra
Publikováno v:
Indian J Surg Oncol
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cfc2621039b350bbf68fd48f66ad738f
https://doi.org/10.1007/s13193-020-01175-7
https://doi.org/10.1007/s13193-020-01175-7
Akademický článek
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Publikováno v:
SA Orthopaedic Journal. 20
BACKGROUND: Multiple hereditary exostosis (MHE) is a rare autosomal dominant disorder predisposing to the development of multiple osteochondromas. Malignant transformation is an uncommon complication of osteochondromas and is especially rare in the p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ffc54da70dcc6fc00d4552fd399f3f3b
https://doi.org/10.17159/2309-8309/2021/v20n3a8
https://doi.org/10.17159/2309-8309/2021/v20n3a8
Autor:
Marina Pacheco, Alberto Righi
Publikováno v:
Journal of Cancer Metastasis and Treatment. 2020
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0ba61e3844d866e586c041e02cac7ec3
https://doi.org/10.20517/2394-4722.2020.85
https://doi.org/10.20517/2394-4722.2020.85
Publikováno v:
eLS
Multiple osteochondromas (MOs) is an autosomal dominant disease characterised by MOs (previously named exostoses). Their formation requires bi-allelic inactivation of EXT1 or EXT2 genes in growth plate cartilage. They encode glycosyltransferases that
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::24ba271ade3f150626cd59218cf4d36f
https://doi.org/10.1002/9780470015902.a0024327
https://doi.org/10.1002/9780470015902.a0024327
Autor:
P.-U. Tunn, M. Werner
Publikováno v:
Der Orthopäde. 44:720-723
A secondary peripheral chondrosarcoma (SPC) evolving from an osteochondroma is rare, but it has been described several times. The development of an osteosarcomatous dedifferentiated chondrosarcoma in a locally recurrent SPC is extremely rare. The fol
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ad1c90c9a423a9edcb84d905d1821385
https://doi.org/10.1007/s00132-015-3143-7
https://doi.org/10.1007/s00132-015-3143-7