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

Year Number of Results
1980 1
1981 2
1983 3
1985 3
1986 2
1987 2
1988 1
1989 4
1990 1
1991 2
1992 2
1993 1
1994 1
1995 1
1996 1
1997 3
1998 2
1999 4
2000 2
2001 2
2002 1
2003 4
2004 1
2005 4
2006 2
2007 3
2008 6
2009 3
2010 3
2011 3
2012 2
2013 3
2014 7
2015 4
2017 3
2018 1
2019 1
2020 3
2022 1
2024 0

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90 results

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Page 1
Management of Myxofibrosarcoma and Undifferentiated Pleomorphic Sarcoma.
Crago AM, Cardona K, Koseła-Paterczyk H, Rutkowski P. Crago AM, et al. Surg Oncol Clin N Am. 2022 Jul;31(3):419-430. doi: 10.1016/j.soc.2022.03.006. Surg Oncol Clin N Am. 2022. PMID: 35715142 Review.
They likely represent a spectrum of disease differentiated by myxoid stroma and curvilinear vessels observed in MFS but not in UPS. Limb-sparing surgery is the standard of care although the infiltrative nature of MFS mandates wider resection margins than are necessary for …
They likely represent a spectrum of disease differentiated by myxoid stroma and curvilinear vessels observed in MFS but not in UPS. Limb-spa …
Primary mesenchymal liver tumors: radiological spectrum, differential diagnosis, and pathologic correlation.
Harman M, Nart D, Acar T, Elmas N. Harman M, et al. Abdom Imaging. 2015 Jun;40(5):1316-30. doi: 10.1007/s00261-014-0268-9. Abdom Imaging. 2015. PMID: 25311993 Review.
The aim of this review was to discuss the clinical, histopathological, and imaging features of liver hemangiomas (cavernous, capillary, and sclerosed types), liver lipoma, angiomyolipoma, mesenchymal hamartoma, neurofibroma, infantile hemangioendothelioma, epithelioid hemangioend …
The aim of this review was to discuss the clinical, histopathological, and imaging features of liver hemangiomas (cavernous, capillary, and …
Retroperitoneal sarcomas: from diagnosis to treatment. Case series and review of the literature.
Mantas D, Garmpis N, Polychroni D, Garmpi A, Damaskos C, Liakea A, Sypsa G, Kouskos E. Mantas D, et al. G Chir. 2020 Jan-Feb;41(1):18-33. G Chir. 2020. PMID: 32038009 Review.
In five patient cases adjuvant therapy was required. Three patients are still alive and free of disease. CONCLUSIONS: Retroperitoneal sarcomas present to be a therapeutic challenge based on their location, their extent at the time of diagnosis and the high risk of l …
In five patient cases adjuvant therapy was required. Three patients are still alive and free of disease. CONCLUSIONS: Retroperitoneal …
The Management of Head and Neck Sarcoma.
Han S, Yin X, Xu W, Wang Y, Han W. Han S, et al. J Craniofac Surg. 2020 Mar/Apr;31(2):e189-e192. doi: 10.1097/SCS.0000000000006162. J Craniofac Surg. 2020. PMID: 31934973
Of soft tissue sarcoma patients, the most frequently observed histologies were fibrosarcoma and malignant fibrous histiocytoma. Of 36 cases of osteogenic sarcoma, osteosarcoma, and fibrosarcoma of bone were most frequent. ...Positive prognostic factors were tumor-free rese …
Of soft tissue sarcoma patients, the most frequently observed histologies were fibrosarcoma and malignant fibrous histiocytoma. Of 36 …
Vulvar sarcomas: Short guideline for histopathological recognition and clinical management. Part 2.
Chokoeva AA, Tchernev G, Cardoso JC, Patterson JW, Dechev I, Valkanov S, Zanardelli M, Lotti T, Wollina U. Chokoeva AA, et al. Int J Immunopathol Pharmacol. 2015 Jun;28(2):178-86. doi: 10.1177/0394632015575977. Epub 2015 Mar 26. Int J Immunopathol Pharmacol. 2015. PMID: 25816393 Free article. Review.
The second part of this review will focus mainly on the rarest variants of vulvar sarcoma: low-grade fibromyxoid sarcoma, synovial sarcoma, monophasic synovial sarcoma, carcinosarcoma, Ewing sarcoma, myeloid sarcoma, dermatofibrosarcoma protuberans, malignant fibrous histiocyt
The second part of this review will focus mainly on the rarest variants of vulvar sarcoma: low-grade fibromyxoid sarcoma, synovial sarcoma, …
Concurrent ifosfamide-based chemotherapy and irradiation. Analysis of treatment-related toxicity in 43 patients with sarcoma.
Cormier JN, Patel SR, Herzog CE, Ballo MT, Burgess MA, Feig BW, Hunt KK, Raney RB, Zagars GK, Benjamin RS, Pisters PW. Cormier JN, et al. Cancer. 2001 Sep 15;92(6):1550-5. doi: 10.1002/1097-0142(20010915)92:6<1550::aid-cncr1481>3.0.co;2-c. Cancer. 2001. PMID: 11745234 Review.
Histologies were rhabdomyosarcoma (n = 16 patients), Ewing sarcoma (n = 10 patients), malignant fibrous histiocytoma (n = 9 patients), and other soft tissue sarcomas (n = 8 patients). ...These results support the design of prospective studies evaluating concurrent ifosfami …
Histologies were rhabdomyosarcoma (n = 16 patients), Ewing sarcoma (n = 10 patients), malignant fibrous histiocytoma (n = 9 patients) …
Primary malignant tumors of the spine.
Sundaresan N, Rosen G, Boriani S. Sundaresan N, et al. Orthop Clin North Am. 2009 Jan;40(1):21-36, v. doi: 10.1016/j.ocl.2008.10.004. Orthop Clin North Am. 2009. PMID: 19064053 Review.
Data from the SEER program suggest that the most common bone sarcomas are osteosarcoma, chondrosarcoma, Ewing's sarcoma, chordoma, and malignant fibrous histiocytoma/fibrosarcoma. During the last two decades, tremendous progress has been made in clinical aspects, surgical …
Data from the SEER program suggest that the most common bone sarcomas are osteosarcoma, chondrosarcoma, Ewing's sarcoma, chordoma, and malig …
Management of adult soft tissue sarcomas of the head and neck.
de Bree R, van der Waal I, de Bree E, Leemans CR. de Bree R, et al. Oral Oncol. 2010 Nov;46(11):786-90. doi: 10.1016/j.oraloncology.2010.09.001. Epub 2010 Oct 13. Oral Oncol. 2010. PMID: 20947413 Review.
Management of these neoplasms presents a great challenge. Malignant fibrous histiocytoma, fibrosarcoma, angiosarcoma and malignant peripheral nerve sheath tumour are the most frequently found sarcoma types in the head and neck. Although traditional morphological assessment …
Management of these neoplasms presents a great challenge. Malignant fibrous histiocytoma, fibrosarcoma, angiosarcoma and malignant pe …
Soft tissue sarcomas: current trends in diagnosis and management.
Antman KH, Eilber FR, Shiu MH. Antman KH, et al. Curr Probl Cancer. 1989 Nov-Dec;13(6):337-67. doi: 10.1016/0147-0272(89)90015-9. Curr Probl Cancer. 1989. PMID: 2689101 Review.
Embryonal rhabdomyosarcoma in the orbit peaks in the 4-year-old, and in the urinary tract in adolescence.2 Osteosarcoma has peak incidence in the teenage years, and Ewing's sarcoma develops between the ages of 15 and 30. Other sarcomas such as malignant fibrous histiocytoma
Embryonal rhabdomyosarcoma in the orbit peaks in the 4-year-old, and in the urinary tract in adolescence.2 Osteosarcoma has peak incidence i …
90 results