Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Results by year

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

Year Number of Results
1964 1
1972 1
1992 1
1995 2
2000 1
2002 1
2003 1
2004 3
2005 5
2006 4
2007 3
2008 5
2009 3
2010 8
2012 1
2013 6
2014 9
2015 9
2016 9
2017 3
2018 14
2019 10
2020 12
2021 21
2022 20
2023 22
2024 9

Text availability

Article attribute

Article type

Publication date

Search Results

162 results

Results by year

Filters applied: . Clear all
Page 1
Evolving classification of rhabdomyosarcoma.
Agaram NP. Agaram NP. Histopathology. 2022 Jan;80(1):98-108. doi: 10.1111/his.14449. Histopathology. 2022. PMID: 34958505 Free PMC article. Review.
Rhabdomyosarcomas comprise the single largest category of soft tissue sarcomas in children and adolescents in the United States, occurring in 4.5 million people aged below 20 years. Based on the clinicopathological features and genetic abnormalities identified, rhabdomy
Rhabdomyosarcomas comprise the single largest category of soft tissue sarcomas in children and adolescents in the United States, occu
Conjunctival Spindle Cell/Sclerosing Rhabdomyosarcoma.
Su YW, Wang LC, Fan NW. Su YW, et al. Ophthalmology. 2023 Oct 24:S0161-6420(23)00705-4. doi: 10.1016/j.ophtha.2023.09.027. Online ahead of print. Ophthalmology. 2023. PMID: 37877920 No abstract available.
Spindle Cell/Sclerosing Rhabdomyosarcoma With PAX8::PPARG Fusion.
Rakheja D, Park JY, Alhasan M, Uddin N. Rakheja D, et al. Int J Surg Pathol. 2022 Dec;30(8):950-955. doi: 10.1177/10668969221095170. Epub 2022 Apr 24. Int J Surg Pathol. 2022. PMID: 35466752
Here we report a spindle cell/sclerosing rhabdomyosarcoma that arose in the orbit of a 4-year-old male. ...Our report adds to the growing number of gene fusions in spindle cell/sclerosing rhabdomyosarcomas....
Here we report a spindle cell/sclerosing rhabdomyosarcoma that arose in the orbit of a 4-year-old male. ...Our report adds to …
Challenges in the Diagnosis of Pediatric Spindle Cell/Sclerosing Rhabdomyosarcoma.
Chen S, Rudzinski ER, Arnold MA. Chen S, et al. Surg Pathol Clin. 2020 Dec;13(4):729-738. doi: 10.1016/j.path.2020.08.010. Epub 2020 Oct 9. Surg Pathol Clin. 2020. PMID: 33183730 Review.
Rhabdomyosarcoma (RMS) is the most common pediatric soft tissue sarcoma, representing approximately 40% of all pediatric soft tissue sarcomas. The spindle cell/sclerosing subtype of RMS (SSRMS) accounts for roughly 5% to 10% of all cases of adult and pediatric RMS.
Rhabdomyosarcoma (RMS) is the most common pediatric soft tissue sarcoma, representing approximately 40% of all pediatric soft tissue
Rhabdomyosarcoma.
Kaseb H, Kuhn J, Babiker HM. Kaseb H, et al. 2022 Jul 18. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2024 Jan–. 2022 Jul 18. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2024 Jan–. PMID: 29939543 Free Books & Documents.
Rhabdomyosarcoma (RMS) is a primitive pediatric malignant soft tissue sarcoma of skeletal muscle phenotype that originates from a primitive mesenchymal cell. ...Rhabdomyosarcoma types include embryonal rhabdomyosarcoma (approximately 60%), alveolar (approxima
Rhabdomyosarcoma (RMS) is a primitive pediatric malignant soft tissue sarcoma of skeletal muscle phenotype that originates from a pri
Spindle Cell/Sclerosing Rhabdomyosarcoma of the Orbit.
Proia AD. Proia AD. Ophthalmic Plast Reconstr Surg. 2023 Jan-Feb 01;39(1):e17-e20. doi: 10.1097/IOP.0000000000002252. Epub 2022 Jul 13. Ophthalmic Plast Reconstr Surg. 2023. PMID: 35829629
Spindle cell/sclerosing rhabdomyosarcoma is an uncommon variant of this neoplasm, and only 2 patients with orbital tumors have been reported in 2 case series. Spindle cell/sclerosing rhabdomyosarcomas confined to the orbit are considered to have an exc …
Spindle cell/sclerosing rhabdomyosarcoma is an uncommon variant of this neoplasm, and only 2 patients with orbital tumors have …
Combined Sclerosing and Spindle Cell Rhabdomyosarcoma in Previous Craniotomy Site: A Case Report and a Review of the Literature.
Gui H, Lhospital E, Staddon AP, Nagda SN, Zager EL, Zhang PJL, Brooks JS. Gui H, et al. Int J Surg Pathol. 2019 May;27(3):328-335. doi: 10.1177/1066896918802030. Epub 2018 Oct 1. Int J Surg Pathol. 2019. PMID: 30270691 Review.
Sclerosing rhabdomyosarcoma (RMS) is a rare subtype of RMS with unique prominent stromal hyalinization and a pseudovascular architecture. ...Sclerosing RMS and spindle RMS likely represent a morphologic spectrum of one entity....
Sclerosing rhabdomyosarcoma (RMS) is a rare subtype of RMS with unique prominent stromal hyalinization and a pseudovascular ar
Sclerosing rhabdomyosarcoma of a chest wall in an adult: a case report and review of the literature.
Mikubo M, Ikeda S, Hoshino T, Yokota T, Fujii A, Mori M. Mikubo M, et al. Ann Thorac Cardiovasc Surg. 2014;20 Suppl:642-5. doi: 10.5761/atcs.cr.13-00030. Epub 2013 Oct 3. Ann Thorac Cardiovasc Surg. 2014. PMID: 24088914 Free article. Review.
Sclerosing rhabdomyosarcoma (SRMS) is a newly recognized and rare variant of rhabdomyosarcoma. ...The tumor cells were positive for muscle markers, and the tumor was diagnosed as rhabdomyosarcoma consistent with a sclerosing type of rhabdomyo
Sclerosing rhabdomyosarcoma (SRMS) is a newly recognized and rare variant of rhabdomyosarcoma. ...The tumor cells were
Non-orbital Sclerosing Rhabdomyosarcoma Presented With Optic Neuropathy.
Hassan MN, Wan Hitam WH, Masnon NA, Nadarajan C. Hassan MN, et al. Cureus. 2022 Jan 9;14(1):e21062. doi: 10.7759/cureus.21062. eCollection 2022 Jan. Cureus. 2022. PMID: 35155025 Free PMC article.
Sclerosing rhabdomyosarcoma presentations are widely variable and non-specific initial features. ...There was also an intracranial extension to the left temporal lobe with the base of skull bone destruction. Transnasal endoscopic biopsy revealed sclerosing
Sclerosing rhabdomyosarcoma presentations are widely variable and non-specific initial features. ...There was also an intracra
Sclerosing rhabdomyosarcoma: report of a case arising in the head and neck of an adult and review of the literature.
Robinson JC, Richardson MS, Neville BW, Day TA, Chi AC. Robinson JC, et al. Head Neck Pathol. 2013 Jun;7(2):193-202. doi: 10.1007/s12105-012-0398-8. Epub 2012 Sep 19. Head Neck Pathol. 2013. PMID: 22990679 Free PMC article. Review.
Sclerosing rhabdomyosarcoma is a unique rhabdomyosarcoma variant, characterized by a prominent hyalinizing matrix. ...Out of 31 cases with follow-up information provided, 6 patients developed local recurrence, 7 patients developed regional or distant metastas
Sclerosing rhabdomyosarcoma is a unique rhabdomyosarcoma variant, characterized by a prominent hyalinizing matrix. ...O
162 results