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

Year Number of Results
1965 1
1975 1
1979 1
1980 2
1981 2
1983 2
1984 1
1985 1
1986 1
1987 3
1990 3
1991 2
1992 2
1994 1
1995 4
1996 2
1997 2
1998 7
1999 7
2000 7
2001 4
2002 3
2003 3
2004 3
2005 3
2006 7
2007 4
2008 6
2009 12
2010 11
2011 9
2012 9
2013 7
2014 8
2015 12
2016 10
2017 16
2018 14
2019 12
2020 12
2021 10
2022 8
2023 13
2024 3

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224 results

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Quoted phrase not found in phrase index: "Advanced Sarcoma of the Extremity"
Page 1
Soft-tissue sarcoma.
Gilbert NF, Cannon CP, Lin PP, Lewis VO. Gilbert NF, et al. J Am Acad Orthop Surg. 2009 Jan;17(1):40-7. doi: 10.5435/00124635-200901000-00006. J Am Acad Orthop Surg. 2009. PMID: 19136426 Review.
Soft-tissue sarcomas of the extremities and pelvis are the most relevant to the orthopaedic surgeon. The patient with extremity soft-tissue sarcoma typically presents with a painless, enlarging mass. ...
Soft-tissue sarcomas of the extremities and pelvis are the most relevant to the orthopaedic surgeon. The patient with extre …
Soft-tissue sarcoma in adults: An update on the current state of histiotype-specific management in an era of personalized medicine.
Gamboa AC, Gronchi A, Cardona K. Gamboa AC, et al. CA Cancer J Clin. 2020 May;70(3):200-229. doi: 10.3322/caac.21605. Epub 2020 Apr 10. CA Cancer J Clin. 2020. PMID: 32275330 Free article. Review.
Soft-tissue sarcomas (STS) are rare tumors that account for 1% of all adult malignancies, with over 100 different histologic subtypes occurring predominately in the trunk, extremity, and retroperitoneum. ...This report summarizes the latest evidence guiding the hist …
Soft-tissue sarcomas (STS) are rare tumors that account for 1% of all adult malignancies, with over 100 different histologic subtypes …
A review of retroperitoneal liposarcoma genomics.
Tyler R, Wanigasooriya K, Taniere P, Almond M, Ford S, Desai A, Beggs A. Tyler R, et al. Cancer Treat Rev. 2020 Jun;86:102013. doi: 10.1016/j.ctrv.2020.102013. Epub 2020 Mar 28. Cancer Treat Rev. 2020. PMID: 32278233 Free article. Review.
Retroperitoneal liposarcomas are rare tumours that carry a poorer prognosis than their extremity counterparts. Within their subtypes - well differentiated (WDL), dedifferentiated (DDL), myxoid (MLS) and pleomorphic (PLS) - they exhibit a diverse genomic landscape. W …
Retroperitoneal liposarcomas are rare tumours that carry a poorer prognosis than their extremity counterparts. Within their su …
A League of Its Own? Established and Emerging Therapies in Undifferentiated Pleomorphic Sarcoma.
Graves L, Jeck WR, Grilley-Olson JE. Graves L, et al. Curr Treat Options Oncol. 2023 Mar;24(3):212-228. doi: 10.1007/s11864-023-01054-7. Epub 2023 Feb 2. Curr Treat Options Oncol. 2023. PMID: 36729198 Review.
Undifferentiated pleomorphic sarcoma (UPS), formerly known as malignant fibrous histiocytoma (MFH), is among the most common subtypes of STS arising in the trunk or extremities of adults. Administration of systemic chemotherapy is the primary management in locally …
Undifferentiated pleomorphic sarcoma (UPS), formerly known as malignant fibrous histiocytoma (MFH), is among the most common subtypes …
Diagnosis and Management of Rhabdomyosarcoma in Children and Adolescents: ICMR Consensus Document.
Panda SP, Chinnaswamy G, Vora T, Prasad M, Bansal D, Kapoor G, Radhakrishnan V, Agarwala S, Laskar S, Arora B, Kaur T, Rath GK, Bakhshi S. Panda SP, et al. Indian J Pediatr. 2017 May;84(5):393-402. doi: 10.1007/s12098-017-2315-3. Epub 2017 Apr 5. Indian J Pediatr. 2017. PMID: 28378141 Review.
Rhabdomyosarcoma (RMS) is a highly malignant tumor which is thought to originate from the pluripotent mesenchyme. It is the most common soft-tissue sarcoma of childhood. This review article summarizes the recent and older published literature and gives an overview of manag …
Rhabdomyosarcoma (RMS) is a highly malignant tumor which is thought to originate from the pluripotent mesenchyme. It is the most common soft …
Distinctive epidemiology and prognosis of de novo and secondary cutaneous angiosarcoma patients.
Ye J, Han W, Xu J. Ye J, et al. Int J Dermatol. 2023 Jul;62(7):952-961. doi: 10.1111/ijd.16673. Epub 2023 Apr 17. Int J Dermatol. 2023. PMID: 37066596
BACKGROUND: Cutaneous angiosarcoma (cAS) is a rare and not well-established malignant neoplasm characterized by dismal prognosis. Treatment for cAS remains controversial. OBJECTIVE: From 1975 to 2016, a total of 872 patients with cAS (379 secondary cAS [s-cAS] patients and …
BACKGROUND: Cutaneous angiosarcoma (cAS) is a rare and not well-established malignant neoplasm characterized by dismal prognosis. Tre …
Soft tissue sarcoma of the extremity: Characterizing symptom duration and outcomes.
Moten AS, Zhao H, Howell K, Nadler A, Reddy SS, von Mehren M, Movva S, Farma JM. Moten AS, et al. Surg Oncol. 2019 Jun;29:190-195. doi: 10.1016/j.suronc.2019.05.016. Epub 2019 May 21. Surg Oncol. 2019. PMID: 31196487
BACKGROUND: We sought to investigate how the interval between symptom onset and diagnosis of soft tissue sarcoma (STS) of the extremity was associated with survival. METHODS: Patients treated for extremity STS years 2006-2015 were stratified by symptom durati …
BACKGROUND: We sought to investigate how the interval between symptom onset and diagnosis of soft tissue sarcoma (STS) of the extr …
The role of regional chemotherapy in the management of extremity soft tissue malignancies.
Smith HG, Hayes AJ. Smith HG, et al. Eur J Surg Oncol. 2016 Jan;42(1):7-17. doi: 10.1016/j.ejso.2015.08.165. Epub 2015 Sep 4. Eur J Surg Oncol. 2016. PMID: 26382102 Review.
The aim of this review was to clarify the roles of each technique in the management of locally advanced soft tissue malignancies of the extremities. METHODS: Relevant articles were identified from a comprehensive literature search using the PubMed database. ...Thoug …
The aim of this review was to clarify the roles of each technique in the management of locally advanced soft tissue malignancies of t …
Leiomyosarcoma: Prognostic outline of a rare head and neck malignancy.
Saluja TS, Iyer J, Singh SK. Saluja TS, et al. Oral Oncol. 2019 Aug;95:100-105. doi: 10.1016/j.oraloncology.2019.06.010. Epub 2019 Jun 13. Oral Oncol. 2019. PMID: 31345375 Review.
Soft tissue sarcomas (STS) are mesenchymal malignant neoplasms with a broad spectrum of biologic behaviour. ...In primary LMS cases, intraoral LMS showed slightly better prognosis than extraoral LMS. Survival analysis revealed that prognosis of primary LMS wa …
Soft tissue sarcomas (STS) are mesenchymal malignant neoplasms with a broad spectrum of biologic behaviour. ...In primary LMS cases, …
The Role of Reconstructive Surgery After Skeletal and Soft Tissue Sarcoma Resection.
Suresh V, Gao J, Jung SH, Brigman B, Eward W, Erdmann D. Suresh V, et al. Ann Plast Surg. 2018 Jun;80(6S Suppl 6):S372-S376. doi: 10.1097/SAP.0000000000001419. Ann Plast Surg. 2018. PMID: 29746275
BACKGROUND: Skeletal and soft tissue reconstruction after sarcoma resection remains challenging. The use of advanced reconstructive techniques has been shown to improve function and increase rates of limb salvage. ...Neoadjuvant radiotherapy was associated with an i …
BACKGROUND: Skeletal and soft tissue reconstruction after sarcoma resection remains challenging. The use of advanced reconstru …
224 results