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Quoted phrase not found in phrase index: "Pediatric mesenchymal chondrosarcoma"
Page 1
Mesenchymal Chondrosarcoma-A Retrospective study.
Beena D, Kattoor J, Mathews A, P Nair S, M V, T P, N G. Beena D, et al. Gulf J Oncolog. 2021 Jan;1(35):54-58. Gulf J Oncolog. 2021. PMID: 33716213
INTRODUCTION: Mesenchymal chondrosarcoma is a rare high grade malignant neoplasm that accounts for 3-10% of all chondrosarcomas. ...The treatment details along with the follow up of the patients were archived from the medical records. RESULTS: A total of 13 cases of …
INTRODUCTION: Mesenchymal chondrosarcoma is a rare high grade malignant neoplasm that accounts for 3-10% of all chondrosarcoma …
Molecular imaging of sarcomas with FDG PET.
Mendoza H, Nosov A, Pandit-Taskar N. Mendoza H, et al. Skeletal Radiol. 2023 Mar;52(3):461-475. doi: 10.1007/s00256-022-04182-7. Epub 2022 Sep 29. Skeletal Radiol. 2023. PMID: 36173459 Review.
Sarcoma comprises a heterogenous entity of musculoskeletal malignancies arising from a mesenchymal origin. The diagnosis and management of pediatric sarcoma requires a multidisciplinary approach and the use of various imaging modalities including CT, MRI and FDG PET …
Sarcoma comprises a heterogenous entity of musculoskeletal malignancies arising from a mesenchymal origin. The diagnosis and manageme …
The Small Round Cell Sarcomas Complexities and Desmoplastic Presentation.
Domanski HA. Domanski HA. Acta Cytol. 2022;66(4):279-294. doi: 10.1159/000524260. Epub 2022 Apr 13. Acta Cytol. 2022. PMID: 35417916 Free PMC article. Review.
BACKGROUND: Small round cell sarcomas (SRCSs) account for most solid malignancies in the pediatric age group and are a part of group of malignant tumors characterized by heterogenous clinical presentation and overlapping microscopic features of small, round, primitive cell …
BACKGROUND: Small round cell sarcomas (SRCSs) account for most solid malignancies in the pediatric age group and are a part of group …
The YAP/TAZ Pathway in Osteogenesis and Bone Sarcoma Pathogenesis.
Kovar H, Bierbaumer L, Radic-Sarikas B. Kovar H, et al. Cells. 2020 Apr 15;9(4):972. doi: 10.3390/cells9040972. Cells. 2020. PMID: 32326412 Free PMC article. Review.
As the extracellular matrix composition and mechanosignaling are of particular relevance in bone formation during embryogenesis, post-natal bone elongation and bone regeneration, YAP/TAZ are believed to have critical functions in these processes. Depending on the differentiation …
As the extracellular matrix composition and mechanosignaling are of particular relevance in bone formation during embryogenesis, post-natal …
Primary intradural extramedullary spinal mesenchymal chondrosarcoma: case report and literature review.
Chen CW, Chen IH, Hu MH, Lee JC, Huang HY, Hong RL, Yang SH. Chen CW, et al. BMC Musculoskelet Disord. 2019 Sep 4;20(1):408. doi: 10.1186/s12891-019-2799-2. BMC Musculoskelet Disord. 2019. PMID: 31484514 Free PMC article. Review.
BACKGROUND: Mesenchymal chondrosarcoma (MCS) is a rare malignant variant of chondrosarcoma with a high tendency of recurrence and metastasis. Intradural extramedullary spinal MCS is exceedingly rare and usually found in pediatric patients. Herein, we p …
BACKGROUND: Mesenchymal chondrosarcoma (MCS) is a rare malignant variant of chondrosarcoma with a high tendency of recu …
Real-world experience of tyrosine kinase inhibitors in children, adolescents and adults with relapsed or refractory bone tumours: A Canadian Sarcoma Research and Clinical Collaboration (CanSaRCC) study.
Peretz Soroka H, Vora T, Noujaim J, Marcoux N, Cohen-Gogo S, Alcindor T, Holloway C, Rodrigues C, Karachiwala H, Alvi S, Lee U, Cheng S, Banerji S, Oberoi S, Feng X, Smrke A, Simmons C, Razak AA, Gupta AA. Peretz Soroka H, et al. Cancer Med. 2023 Sep;12(18):18872-18881. doi: 10.1002/cam4.6515. Epub 2023 Sep 19. Cancer Med. 2023. PMID: 37724607 Free PMC article.
OBJECTIVES: We conducted a retrospective multi-centre study to assess the real-world outcome of regorafenib (REGO) and cabozantinib (CABO) in recurrent/refractory bone tumours (BTs) including osteosarcoma (OST), Ewing sarcoma (EWS) and chondrosarcoma (CS)/extra-skeletal …
OBJECTIVES: We conducted a retrospective multi-centre study to assess the real-world outcome of regorafenib (REGO) and cabozantinib (CABO) i …
Intraspinal mesenchymal chondrosarcoma: report of a pediatric case and literature review.
Di Giannatale A, Colletti M, Russo I, Ferruzzi V, Dell' Anna VA, Cozza R, Colafati GS, Messina R, Mastronuzzi A, De Vito R, Milano GM. Di Giannatale A, et al. Tumori. 2017 Nov 15;103(Suppl. 1):e66-e72. doi: 10.5301/tj.5000689. Tumori. 2017. PMID: 29143958
PURPOSE: Mesenchymal chondrosarcoma (MCS) is an aggressive variant of chondrosarcoma and is a rare tumor, particularly within the pediatric population. ...The tumor was documented by magnetic resonance imaging and treated with gross total resection (GT …
PURPOSE: Mesenchymal chondrosarcoma (MCS) is an aggressive variant of chondrosarcoma and is a rare tumor, particularly …
Primary chondrosarcoma of the head and neck in pediatric patients: a clinicopathologic study of 14 cases with a review of the literature.
Gadwal SR, Fanburg-Smith JC, Gannon FH, Thompson LD. Gadwal SR, et al. Cancer. 2000 May 1;88(9):2181-8. Cancer. 2000. PMID: 10813732 Review.
BACKGROUND: Primary chondrosarcoma of the head and neck in the pediatric age group is rare. ...Follow-up was available for 11 patients; all were alive (at a mean of 14.8 years), with only a single patient demonstrating evidence of residual/ recurrent tumor (at 16.6 …
BACKGROUND: Primary chondrosarcoma of the head and neck in the pediatric age group is rare. ...Follow-up was available for 11 …
Intracranial extra-axial mesenchymal chondrosarcoma in a 16-month-old patient with a literature review of pediatric patients.
Yapıcıer Ö, Nanah AR, Taskapılıoglu MÖ, Demir MK. Yapıcıer Ö, et al. Childs Nerv Syst. 2021 Feb;37(2):649-657. doi: 10.1007/s00381-020-04652-0. Epub 2020 May 8. Childs Nerv Syst. 2021. PMID: 32382867 Review.
Mesenchymal chondrosarcoma is a rare high-grade malignant subtype of chondrosarcoma that is characterized by undifferentiated, round, or spindled mesenchymal cells, interspersed with islands of hyaline cartilage. We report a primary intracranial extra- …
Mesenchymal chondrosarcoma is a rare high-grade malignant subtype of chondrosarcoma that is characterized by undifferen …
Sacral mesenchymal chondrosarcoma in childhood: a case report and review of the literature.
Küpeli S, Varan A, Gedikoğlu G, Büyükpamukçu M. Küpeli S, et al. Pediatr Hematol Oncol. 2010 Oct;27(7):564-73. doi: 10.3109/08880018.2010.503333. Pediatr Hematol Oncol. 2010. PMID: 20677924 Review.
Mesenchymal chondrosarcomas are rare malignant tumors in pediatric age group. ...According to the authors' literature search, the patient is the first reported case of pediatric sacral primary mesenchymal chondrosarcoma. Mesenchymal ch …
Mesenchymal chondrosarcomas are rare malignant tumors in pediatric age group. ...According to the authors' literature search, …
31 results