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

Year Number of Results
1977 1
1978 1
1979 2
1983 1
1985 2
1986 2
1987 2
1988 1
1989 1
1990 3
1991 2
1993 1
1995 6
1996 4
1997 7
1998 9
1999 4
2000 10
2001 5
2002 7
2003 7
2004 11
2005 10
2006 15
2007 12
2008 12
2009 12
2010 12
2011 19
2012 15
2013 14
2014 12
2015 17
2016 15
2017 17
2018 18
2019 20
2020 23
2021 16
2022 23
2023 26
2024 6

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353 results

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Page 1
The many faces of solitary fibrous tumor; diversity of histological features, differential diagnosis and role of molecular studies and surrogate markers in avoiding misdiagnosis and predicting the behavior.
Tariq MU, Din NU, Abdul-Ghafar J, Park YK. Tariq MU, et al. Diagn Pathol. 2021 Apr 20;16(1):32. doi: 10.1186/s13000-021-01095-2. Diagn Pathol. 2021. PMID: 33879215 Free PMC article. Review.
BACKGROUND: Solitary Fibrous Tumor (SFT) is a distinct soft tissue neoplasm associated with NAB2-STAT6 gene fusion. It can involve a number of anatomic sites and exhibits a wide spectrum of histological features. ...
BACKGROUND: Solitary Fibrous Tumor (SFT) is a distinct soft tissue neoplasm associated with NAB2-STAT6 gene fusion. It …
Atypical Spindle Cell/Pleomorphic Lipomatous Tumor.
Qorbani A, Horvai A. Qorbani A, et al. Surg Pathol Clin. 2024 Mar;17(1):97-104. doi: 10.1016/j.path.2023.07.004. Epub 2023 Aug 23. Surg Pathol Clin. 2024. PMID: 38278611 Review.
Atypical spindle cell/pleomorphic lipomatous tumor (ASCPLT) is a rare soft tissue neoplasm, commonly arising in the subcutis (more common than deep soft tissue) of limbs and limb girdles during mid-adulthood. ...
Atypical spindle cell/pleomorphic lipomatous tumor (ASCPLT) is a rare soft tissue neoplasm, commonly arising in the sub …
Current Update on Desmoid Fibromatosis.
Ganeshan D, Amini B, Nikolaidis P, Assing M, Vikram R. Ganeshan D, et al. J Comput Assist Tomogr. 2019 Jan-Feb;43(1):29-38. doi: 10.1097/RCT.0000000000000790. J Comput Assist Tomogr. 2019. PMID: 30211798 Free PMC article. Review.
Recent advances in the management of desmoid fibromatosis will also be discussed. CONCLUSIONS: Desmoid fibromatosis is a rare soft tissue neoplasm with a high incidence of local recurrence. Imaging plays an important role in the diagnosis and management of th …
Recent advances in the management of desmoid fibromatosis will also be discussed. CONCLUSIONS: Desmoid fibromatosis is a rare soft …
Soft tissue tumor diagnosis: A three prong approach utilizing pattern analysis, immunocytochemistry, and molecular diagnostics.
Layfield LJ. Layfield LJ. Diagn Cytopathol. 2020 Mar;48(3):265-284. doi: 10.1002/dc.24355. Epub 2019 Dec 23. Diagn Cytopathol. 2020. PMID: 31868988 Review.
Tissue diagnosis of a soft tissue neoplasm is of paramount importance for the development of an appropriate treatment plan. ...
Tissue diagnosis of a soft tissue neoplasm is of paramount importance for the development of an appropriate treatment p …
INternational Soft Tissue saRcoma ConsorTium (INSTRuCT) consensus statement: Imaging recommendations for the management of rhabdomyosarcoma.
Schoot RA, van Ewijk R, von Witzleben AA, Kao SC, Merks JHMH, Morosi C, Pace E, Shulkin BL, Ferrari A, von Kalle T, van Rijn RR, Weiss AR, Sparber-Sauer M, Ter Horst SAJ, McCarville MB. Schoot RA, et al. Eur J Radiol. 2023 Sep;166:111012. doi: 10.1016/j.ejrad.2023.111012. Epub 2023 Jul 25. Eur J Radiol. 2023. PMID: 37541182 Review.
Rhabdomyosarcoma is the most common soft-tissue neoplasm in the pediatric population. The survival of children with rhabdomyosarcoma has only marginally improved over the past 25 years and remains poor for those with metastatic disease. ...
Rhabdomyosarcoma is the most common soft-tissue neoplasm in the pediatric population. The survival of children with rha …
Primary Tumors of the Foot and Ankle.
Kennedy JG, Ross KA, Smyth NA, Hogan MV, Murawski CD. Kennedy JG, et al. Foot Ankle Spec. 2016 Feb;9(1):58-68. doi: 10.1177/1938640015620634. Epub 2015 Dec 7. Foot Ankle Spec. 2016. PMID: 26644034 Review.
Epithelioid Sarcoma: Diagnostic Features and Genetics.
Thway K, Jones RL, Noujaim J, Fisher C. Thway K, et al. Adv Anat Pathol. 2016 Jan;23(1):41-9. doi: 10.1097/PAP.0000000000000102. Adv Anat Pathol. 2016. PMID: 26645461 Review.
Epithelioid sarcoma (ES) is a rare, aggressive soft-tissue neoplasm of uncertain differentiation, characterized by nodular aggregates of epithelioid cells, which are immunoreactive to cytokeratins (CKs) and epithelial membrane antigen, and often for CD34. ...
Epithelioid sarcoma (ES) is a rare, aggressive soft-tissue neoplasm of uncertain differentiation, characterized by nodu …
Ossifying Fibromyxoid Tumor: An Update.
Bakiratharajan D, Rekhi B. Bakiratharajan D, et al. Arch Pathol Lab Med. 2016 Apr;140(4):371-5. doi: 10.5858/arpa.2014-0590-RS. Arch Pathol Lab Med. 2016. PMID: 27028395 Free article. Review.
Ossifying fibromyxoid tumor (OFMT) is a rare soft tissue neoplasm of uncertain differentiation, initially described by Enzinger and colleagues. ...
Ossifying fibromyxoid tumor (OFMT) is a rare soft tissue neoplasm of uncertain differentiation, initially described by …
Osteolipoma of head and neck - a review.
Wong BLK, Hogan C. Wong BLK, et al. Braz J Otorhinolaryngol. 2022 Nov-Dec;88 Suppl 4(Suppl 4):S177-S187. doi: 10.1016/j.bjorl.2022.04.002. Epub 2022 May 20. Braz J Otorhinolaryngol. 2022. PMID: 35659712 Free PMC article. Review.
Only 1 regrowth was reported after 5-years. CONCLUSIONS: Osteolipoma is a rare soft tissue neoplasm which has a wide range differential diagnosis including malignant processes. ...
Only 1 regrowth was reported after 5-years. CONCLUSIONS: Osteolipoma is a rare soft tissue neoplasm which has a wide ra …
A Review of Effusion Cytomorphology of Small Round Cell Tumors.
Han LM, VandenBussche CJ, Abildtrup M, Chandra A, Vohra P. Han LM, et al. Acta Cytol. 2022;66(4):336-346. doi: 10.1159/000516497. Epub 2021 Jul 2. Acta Cytol. 2022. PMID: 34218227 Review.
In contrast, synovial sarcoma typically involves extremities and expresses a fusion transcript in t(X;18) (SS18-SSX). This soft tissue neoplasm demonstrates uniform cells with irregular nuclear contours, characteristic nuclear folding, and scant cytoplasm. .. …
In contrast, synovial sarcoma typically involves extremities and expresses a fusion transcript in t(X;18) (SS18-SSX). This soft ti …
353 results