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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
1976 1
1979 1
1981 1
1983 1
1986 3
1987 4
1988 4
1989 3
1990 1
1991 1
1992 2
1993 3
1994 3
1995 3
1996 3
1998 3
1999 6
2000 4
2001 2
2002 7
2003 5
2004 3
2005 1
2006 1
2007 3
2008 4
2009 1
2010 2
2012 4
2013 2
2014 5
2015 2
2016 6
2017 3
2018 4
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2020 6
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2022 7
2023 3
2024 0

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124 results

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Page 1
Primary intratesticular rhabdomyosarcoma in children: a case report and review of the literature.
Yahaya JJ, Mremi A. Yahaya JJ, et al. J Med Case Rep. 2021 Jan 31;15(1):37. doi: 10.1186/s13256-020-02599-z. J Med Case Rep. 2021. PMID: 33516251 Free PMC article. Review.
BACKGROUND: The importance of this paper is to help to emphasize the importance of chemotherapy for children with pure intratesticular rhabdomyosarcoma after radical inguinal orchiectomy is done as first treatment of rhabdomyosarcoma. ...Pelvic computer tomography ( …
BACKGROUND: The importance of this paper is to help to emphasize the importance of chemotherapy for children with pure intratesticular rh
Molecular testing of rhabdomyosarcoma in clinical trials to improve risk stratification and outcome: A consensus view from European paediatric Soft tissue sarcoma Study Group, Children's Oncology Group and Cooperative Weichteilsarkom-Studiengruppe.
Hettmer S, Linardic CM, Kelsey A, Rudzinski ER, Vokuhl C, Selfe J, Ruhen O, Shern JF, Khan J, Kovach AR, Lupo PJ, Gatz SA, Schäfer BW, Volchenboum S, Minard-Colin V, Koscielniak E, Hawkins DS, Bisogno G, Sparber-Sauer M, Venkatramani R, Merks JHM, Shipley J. Hettmer S, et al. Eur J Cancer. 2022 Sep;172:367-386. doi: 10.1016/j.ejca.2022.05.036. Epub 2022 Jul 12. Eur J Cancer. 2022. PMID: 35839732 Free article. Review.
Rhabdomyosarcomas (RMSs) are the most common soft tissue sarcomas in children/adolescents less than 18 years of age with an annual incidence of 1-2/million. Inter/intra-tumour heterogeneity raise challenges in clinical, pathological and biological research studies. ...In p …
Rhabdomyosarcomas (RMSs) are the most common soft tissue sarcomas in children/adolescents less than 18 years of age with an annual incidence …
Uterine sarcomas and rare uterine mesenchymal tumors with malignant potential. Diagnostic guidelines of the French Sarcoma Group and the Rare Gynecological Tumors Group.
Croce S, Devouassoux-Shisheboran M, Pautier P, Ray-Coquard I, Treilleux I, Neuville A, Arnould L, Just PA, Belda MALF, Averous G, Leroux A, Mery E, Loussouarn D, Weinbreck N, Le Guellec S, Mishellany F, Morice P, Guyon F, Genestie C. Croce S, et al. Gynecol Oncol. 2022 Nov;167(2):373-389. doi: 10.1016/j.ygyno.2022.07.031. Epub 2022 Sep 14. Gynecol Oncol. 2022. PMID: 36114030 Review.
Uterine PEComa has a specific algorithm stratifying the tumors into uncertain malignant potential and malignant tumors. Embryonal rhabdomyosarcomas of the uterine cervix are not restricted to children but can also be observed in adult women and are almost always DICER1 mut …
Uterine PEComa has a specific algorithm stratifying the tumors into uncertain malignant potential and malignant tumors. Embryonal rha …
Metastatic embryonal rhabdomyosarcoma of the breast: A case report and literature review.
Ma X, Chen X, Jiang G, Jiang L, Li T, Wei L, Li S. Ma X, et al. Breast J. 2021 Dec;27(12):890-894. doi: 10.1111/tbj.14284. Epub 2021 Oct 21. Breast J. 2021. PMID: 34672049 Review.
Rhabdomyosarcoma (RMS) is a common malignancy in children, but embryonal rhabdomyosarcoma (ERMS) deposits rarely occur in the breast in adults. Therefore, little is known about magnetic resonance imaging (MRI) features of breast metastases from RMS, especiall
Rhabdomyosarcoma (RMS) is a common malignancy in children, but embryonal rhabdomyosarcoma (ERMS) deposits rarely occur
Adult laryngeal Embryonal Rhabdomyosarcoma: a case report and literature review.
Hu J, Lu D, Ren J, Wen Q, Zhou J, Gan W, Liu J, Liu S, Yang H, Zou J. Hu J, et al. BMC Surg. 2020 Jul 31;20(1):173. doi: 10.1186/s12893-020-00831-7. BMC Surg. 2020. PMID: 32736545 Free PMC article. Review.
Consequently, less information was available to guide clinicians to manage adult RMSs in larynx. CASE PRESENTATION: A 42-year-old man presented with a 2-year history of gradually worsening hoarseness. Then, he underwent a surgery with suspension laryngoscope with initially …
Consequently, less information was available to guide clinicians to manage adult RMSs in larynx. CASE PRESENTATION: A 42-year-old man presen …
Molecular characterization of an embryonal rhabdomyosarcoma occurring in a patient with Kabuki syndrome: report and literature review in the light of tumor predisposition syndromes.
Aukema SM, Glaser S, van den Hout MFCM, Dahlum S, Blok MJ, Hillmer M, Kolarova J, Sciot R, Schott DA, Siebert R, Stumpel CTRM. Aukema SM, et al. Fam Cancer. 2023 Jan;22(1):103-118. doi: 10.1007/s10689-022-00306-z. Epub 2022 Jul 19. Fam Cancer. 2023. PMID: 35856126 Free PMC article. Review.
Here we report on a female patient with Kabuki syndrome and a c.2558_2559delCT germline variant in KMT2D who developed an embryonal rhabdomyosarcoma (ERMS) at 10 years. On tumor tissue we performed DNA-methylation profiling and exome sequencing (ES). Copy number ana …
Here we report on a female patient with Kabuki syndrome and a c.2558_2559delCT germline variant in KMT2D who developed an embryonal
Embryonal rhabdomyosarcoma of the uterine cervix in adults: a case report and literature review.
Ditto A, Martinelli F, Carcangiu M, Solima E, de Carrillo KJ, Sanfilippo R, Haeusler E, Raspagliesi F. Ditto A, et al. J Low Genit Tract Dis. 2013 Oct;17(4):e12-7. doi: 10.1097/LGT.0b013e31827a8b8c. J Low Genit Tract Dis. 2013. PMID: 23903199 Review.
OBJECTIVE: We report a case of cervical rhabdomyosarcoma in an adult and review of literature. MATERIALS AND METHODS: A 44-year-old, premenopausal, white woman, complained of vaginal bleeding for 2 months. ...The polyp was partially removed by polypectomy. Pathologi …
OBJECTIVE: We report a case of cervical rhabdomyosarcoma in an adult and review of literature. MATERIALS AND METHODS: A 44-year-old, …
Molecular profile of head and neck rhabdomyosarcomas: A systematic review and meta-analysis.
Gallagher KPD, van Heerden W, Said-Al-Naief N, Carlos R, Arboleda LPA, Rodrigues-Fernandes CI, Araújo ALD, Fonseca FP, Pontes HAR, Innocentini LMAR, Romañach MJ, Vargas PA, Lopes MA, Santos-Silva AR, Khurram SA. Gallagher KPD, et al. Oral Surg Oral Med Oral Pathol Oral Radiol. 2022 Sep;134(3):354-366. doi: 10.1016/j.oooo.2021.12.128. Epub 2021 Dec 25. Oral Surg Oral Med Oral Pathol Oral Radiol. 2022. PMID: 35840496 Review.
RESULTS: HNRMS predominantly affects pediatric patients (44.4%), and the parameningeal region (57.7%) is the most common location. The alveolar variant (43.2%) predominates over the embryonal and spindle cell/sclerosing types, followed by the epithelioid and pleomor …
RESULTS: HNRMS predominantly affects pediatric patients (44.4%), and the parameningeal region (57.7%) is the most common location. The alveo …
Congenital spindle cell rhabdomyosarcoma.
Whittle SB, Hicks MJ, Roy A, Vasudevan SA, Reddy K, Venkatramani R. Whittle SB, et al. Pediatr Blood Cancer. 2019 Nov;66(11):e27935. doi: 10.1002/pbc.27935. Epub 2019 Jul 24. Pediatr Blood Cancer. 2019. PMID: 31339226 Review.
Spindle cell and sclerosing rhabdomyosarcoma (ssRMS) is a rare variant of rhabdomyosarcoma, which includes three distinct subtypes. ...We present four cases of ssRMS and 16 additional cases from the literature, which show that these patients present with localized d …
Spindle cell and sclerosing rhabdomyosarcoma (ssRMS) is a rare variant of rhabdomyosarcoma, which includes three distinct subt …
Embryonal rhabdomyosarcoma of the chest wall: a case report and review of the literature.
Mysorekar VV, Harish K, Kilara N, Subramanian M, Giridhar AG. Mysorekar VV, et al. Indian J Pathol Microbiol. 2008 Apr-Jun;51(2):274-6. doi: 10.4103/0377-4929.41694. Indian J Pathol Microbiol. 2008. PMID: 18603708 Review.
Embryonal rhabdomyosarcoma is a soft-tissue sarcoma which has a predilection for the head and neck area, genitourinary tract and the extremities. We report a rare case of embryonal rhabdomyosarcoma of the chest wall in an 8-year-old girl, presenting as
Embryonal rhabdomyosarcoma is a soft-tissue sarcoma which has a predilection for the head and neck area, genitourinary tract a
124 results