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1963
2025

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1963 1
1977 1
1978 1
1979 2
1984 1
1987 1
1988 4
1989 3
1990 2
1991 1
1992 2
1993 3
1994 5
1995 6
1996 5
1997 6
1998 8
1999 7
2000 9
2001 6
2002 6
2003 5
2004 6
2005 3
2006 2
2007 8
2008 4
2009 5
2010 8
2011 6
2012 10
2013 8
2014 6
2015 6
2016 7
2017 5
2018 9
2019 12
2020 15
2021 12
2022 7
2023 4
2024 6
2025 0

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212 results

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Page 1
The 2020 WHO Classification of Tumors of Bone: An Updated Review.
Choi JH, Ro JY. Choi JH, et al. Adv Anat Pathol. 2021 May 1;28(3):119-138. doi: 10.1097/PAP.0000000000000293. Adv Anat Pathol. 2021. PMID: 33480599 Review.
The diversity and considerable morphologic overlap of bone tumors with other mesenchymal and nonmesenchymal bone lesions can complicate diagnosis. Accurate histologic diagnosis is crucial for appropriate management and prognostication. ...
The diversity and considerable morphologic overlap of bone tumors with other mesenchymal and nonmesenchymal bone lesions can complica …
The epigenomics of sarcoma.
Nacev BA, Jones KB, Intlekofer AM, Yu JSE, Allis CD, Tap WD, Ladanyi M, Nielsen TO. Nacev BA, et al. Nat Rev Cancer. 2020 Oct;20(10):608-623. doi: 10.1038/s41568-020-0288-4. Epub 2020 Aug 11. Nat Rev Cancer. 2020. PMID: 32782366 Free PMC article. Review.
Alterations in genes that encode chromatin regulators are common among mesenchymal neoplasms, a collection of more than 160 tumour types including over 60 malignant variants (sarcomas) that have unique and varied genetic, biological and clinical characteristics. ...Epigene …
Alterations in genes that encode chromatin regulators are common among mesenchymal neoplasms, a collection of more than 160 tumour ty …
Ewing sarcoma and Ewing-like tumors.
Sbaraglia M, Righi A, Gambarotti M, Dei Tos AP. Sbaraglia M, et al. Virchows Arch. 2020 Jan;476(1):109-119. doi: 10.1007/s00428-019-02720-8. Epub 2019 Dec 4. Virchows Arch. 2020. PMID: 31802230 Review.
Ewing sarcoma (ES) and Ewing-like sarcomas are highly aggressive round cell mesenchymal neoplasms, most often occurring in children and young adults. The identification of novel molecular alterations has greatly contributed to a profound reappraisal of classification, to t …
Ewing sarcoma (ES) and Ewing-like sarcomas are highly aggressive round cell mesenchymal neoplasms, most often occurring in children a …
SWI/SNF complex-deficient soft tissue neoplasms: An update.
Schaefer IM, Hornick JL. Schaefer IM, et al. Semin Diagn Pathol. 2021 May;38(3):222-231. doi: 10.1053/j.semdp.2020.05.005. Epub 2020 Jun 5. Semin Diagn Pathol. 2021. PMID: 32646614 Free PMC article. Review.
In addition, subsets of myoepithelial carcinoma (10-40%), extraskeletal myxoid chondrosarcoma (20%), epithelioid schwannoma (40%), and epithelioid malignant peripheral nerve sheath tumor (70%) demonstrate SMARCB1 loss. ...
In addition, subsets of myoepithelial carcinoma (10-40%), extraskeletal myxoid chondrosarcoma (20%), epithelioid schwannoma (40%), an …
Extraskeletal Mesenchymal Chondrosarcoma.
Arora K, Riddle ND. Arora K, et al. Arch Pathol Lab Med. 2018 Nov;142(11):1421-1424. doi: 10.5858/arpa.2017-0109-RS. Arch Pathol Lab Med. 2018. PMID: 30407856 Free article. Review.
Extraskeletal mesenchymal chondrosarcoma is a rare soft tissue sarcoma arising from soft tissues, mainly of the lower extremities, meninges, and orbits. ...
Extraskeletal mesenchymal chondrosarcoma is a rare soft tissue sarcoma arising from soft tissues, mainly of the lower extremit …
Malignant Cartilage-Forming Tumors.
Hameed M. Hameed M. Surg Pathol Clin. 2021 Dec;14(4):605-617. doi: 10.1016/j.path.2021.06.005. Epub 2021 Oct 7. Surg Pathol Clin. 2021. PMID: 34742483 Review.
Subtypes include conventional (75%), dedifferentiated (10%), clear cell (2%), mesenchymal (2%), and periosteal chondrosarcoma (<1%). Tumor location and primary vs secondary also play a role. In conventional chondrosarcoma, histologic grading (I, II, and II …
Subtypes include conventional (75%), dedifferentiated (10%), clear cell (2%), mesenchymal (2%), and periosteal chondrosarcoma
Sarcoma.
Skubitz KM, D'Adamo DR. Skubitz KM, et al. Mayo Clin Proc. 2007 Nov;82(11):1409-32. doi: 10.4065/82.11.1409. Mayo Clin Proc. 2007. PMID: 17976362 Review.
Sarcomas comprise a heterogeneous group of mesenchymal neoplasms. They can be grouped into 2 general categories, soft tissue sarcoma and primary bone sarcoma, which have different staging and treatment approaches. This review includes a discussion of both soft tissue sarco …
Sarcomas comprise a heterogeneous group of mesenchymal neoplasms. They can be grouped into 2 general categories, soft tissue sarcoma …
Rare case report and literature review of intracranial mesenchymal chondrosarcoma.
Fu LY, Han Q, Cheng P, Yang HJ, Zhao Y. Fu LY, et al. Ann Palliat Med. 2021 Nov;10(11):12012-12017. doi: 10.21037/apm-21-2290. Ann Palliat Med. 2021. PMID: 34872324 Free article. Review.
Intracranial mesenchymal chondrosarcoma (IMC) is a rare primary malignant tumor in the skull, but mostly originates from the abnormal residual chondrocytes in the embryonic period, which grow slowly, and primarily occurs at the junction of the cartilage of the skull …
Intracranial mesenchymal chondrosarcoma (IMC) is a rare primary malignant tumor in the skull, but mostly originates from the a …
Mesenchymal Chondrosarcoma: a Review with Emphasis on its Fusion-Driven Biology.
El Beaino M, Roszik J, Livingston JA, Wang WL, Lazar AJ, Amini B, Subbiah V, Lewis V, Conley AP. El Beaino M, et al. Curr Oncol Rep. 2018 Mar 26;20(5):37. doi: 10.1007/s11912-018-0668-z. Curr Oncol Rep. 2018. PMID: 29582189 Review.
Mesenchymal chondrosarcoma is a rare but deadly form of chondrosarcoma that typically affects adolescents and young adults. ...This manuscript will briefly review the clinical and pathologic features of mesenchymal chondrosarcoma followed by an
Mesenchymal chondrosarcoma is a rare but deadly form of chondrosarcoma that typically affects adolescents and young adu
Cartilage-forming tumors.
Qasem SA, DeYoung BR. Qasem SA, et al. Semin Diagn Pathol. 2014 Jan;31(1):10-20. doi: 10.1053/j.semdp.2014.01.006. Epub 2014 Jan 23. Semin Diagn Pathol. 2014. PMID: 24680178 Review.
The morphologic heterogeneity of these tumors may be explained by a common multipotent mesenchymal cell differentiating along the lines of fetal-adult cartilage maturation. Recently mutations in IDH1 and IDH2 have been detected in a variety of benign and malignant cartilag …
The morphologic heterogeneity of these tumors may be explained by a common multipotent mesenchymal cell differentiating along the lin …
212 results