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The following term was not found in PubMed: Tissues3A
Page 1
Primary extraskeletal myxoid chondrosarcoma of the breast: report of a case and literature review.
Sharma S, Lobo A, Sharma A, Sampat NY, Kumar M, Kajla R, Mohapatra SS, Mohanty SK. Sharma S, et al. Pathologica. 2022 Jun;114(3):228-237. doi: 10.32074/1591-951X-303. Pathologica. 2022. PMID: 35775709 Free PMC article. Review.
Mammogram revealed a fairly circumscribed mass with spicules of calcifications. The core biopsy and resection specimen showed a myxoid soft tissue neoplasm with histologic features of a myxoid chondrosarcoma. ...In conclusion, surgical pathologists should include EMC in th …
Mammogram revealed a fairly circumscribed mass with spicules of calcifications. The core biopsy and resection specimen showed a myxoid so …
Paravertebral extraskeletal myxoid chondrosarcoma: a case report and review of the literature.
Farhane FZ, Alami Z, Bouhafa T, Elmazghi A, Hassouni K. Farhane FZ, et al. Pan Afr Med J. 2015 Jul 23;21:213. doi: 10.11604/pamj.2015.21.213.6639. eCollection 2015. Pan Afr Med J. 2015. PMID: 26448808 Free PMC article. Review.
The extraskeletal myxoid chondrosarcoma (CME) is a rare malignant soft tissue tumour described as a distinct clinical, histological, immunohistochemical, genetical and evolutive entity. It represents only 2.5% of soft tissue sarcomas. Its individualization is import …
The extraskeletal myxoid chondrosarcoma (CME) is a rare malignant soft tissue tumour described as a distinct clinical, histological, …
Extraskeletal Myxoid Chondrosarcoma: State of the Art and Current Research on Biology and Clinical Management.
Stacchiotti S, Baldi GG, Morosi C, Gronchi A, Maestro R. Stacchiotti S, et al. Cancers (Basel). 2020 Sep 21;12(9):2703. doi: 10.3390/cancers12092703. Cancers (Basel). 2020. PMID: 32967265 Free PMC article. Review.
Extraskeletal myxoid chondrosarcoma (EMC) is an ultra-rare mesenchymal neoplasm with uncertain differentiation, which arises mostly in the deep soft tissue of proximal extremities and limb girdles. EMC is marked by a translocation involving the NR4A3 gene, which can be fus …
Extraskeletal myxoid chondrosarcoma (EMC) is an ultra-rare mesenchymal neoplasm with uncertain differentiation, which arises mostly in the d …
Primary extraskeletal myxoid chondrosarcoma of bone: Report of three cases and review of the literature.
Finos L, Righi A, Frisoni T, Gambarotti M, Ghinelli C, Benini S, Vanel D, Picci P. Finos L, et al. Pathol Res Pract. 2017 May;213(5):461-466. doi: 10.1016/j.prp.2017.02.008. Epub 2017 Feb 11. Pathol Res Pract. 2017. PMID: 28249774 Review.
Extraskeletal myxoid chondrosarcoma is a rare neoplasm of soft tissue. The usual location is in deep parts of the proximal extremities and limb girdles in middle-aged adults. ...Tumors arose in the iliac bone in two cases and in the proximal humerus in the other case. At t …
Extraskeletal myxoid chondrosarcoma is a rare neoplasm of soft tissue. The usual location is in deep parts of the proximal extremitie …
Extraskeletal myxoid chondrosarcoma: updated clinicopathological and molecular genetic characteristics.
Hisaoka M, Hashimoto H. Hisaoka M, et al. Pathol Int. 2005 Aug;55(8):453-63. doi: 10.1111/j.1440-1827.2005.01853.x. Pathol Int. 2005. PMID: 15998372 Review.
Extraskeletal myxoid chondrosarcoma (EMC) is a rare soft-tissue sarcoma characterized by distinctive morphological and cytogenetical features. As its name implies, EMC was believed to represent a variant of soft-tissue chondrosarcoma owing to its histological resemb …
Extraskeletal myxoid chondrosarcoma (EMC) is a rare soft-tissue sarcoma characterized by distinctive morphological and cytogenetical …
[Extraskeletal myxoid chondrosarcoma: a report of 5 cases and review of literature].
Xu H, Yang C, Wang Y, Yang S. Xu H, et al. Zhonghua Bing Li Xue Za Zhi. 2014 Jan;43(1):30-3. Zhonghua Bing Li Xue Za Zhi. 2014. PMID: 24713246 Review. Chinese.
Their age ranged from 38 to 63 years (average = 51 years). The patients primarily presented with a tender soft tissue mass. All the tumors studied were solitary and the duration of disease onset varied from 3 months to 1 year. ...CD117 showed diffuse positivity in case 1, …
Their age ranged from 38 to 63 years (average = 51 years). The patients primarily presented with a tender soft tissue mass. All the t …
18 results