Epidemiology, incidence, and survival of rhabdomyosarcoma subtypes: SEER and ICES database analysis
KM Amer, JE Thomson, D Congiusta… - Journal of …, 2019 - Wiley Online Library
Rhabdomyosarcoma is the most common soft‐tissue sarcoma in children and adolescents
and accounts for 3% of all pediatric tumors. Subtypes include alveolar, spindle cell …
and accounts for 3% of all pediatric tumors. Subtypes include alveolar, spindle cell …
[HTML][HTML] Practical Management of Adult Ultra-Rare Primary Retroperitoneal Soft Tissue Sarcoma: A Focus on Perivascular Epithelioid Tumours and Extraosseous …
SS Apte, E Mor, C Mitchell, DE Gyorki - Current Oncology, 2023 - mdpi.com
With the exception of well-differentiated liposarcoma, dedifferentiated liposarcoma,
leiomyosarcoma, solitary fibrous tumour, malignant peripheral nerve sheath tumour, and …
leiomyosarcoma, solitary fibrous tumour, malignant peripheral nerve sheath tumour, and …
[HTML][HTML] Machine learning model for predicting postoperative survival of patients with colorectal cancer
Purpose Machine learning (ML) is a strong candidate for making accurate predictions, as we
can use large amount of data with powerful computational algorithms. We developed a ML …
can use large amount of data with powerful computational algorithms. We developed a ML …
[HTML][HTML] Deciphering the genomic landscape and pharmacological profile of uncommon entities of adult rhabdomyosarcomas
Adult rhabdomyosarcoma (RMS) represents an uncommon entity with an incidence of less
than 3% of all soft tissue sarcomas (STS). Consequently, the natural history and the clinical …
than 3% of all soft tissue sarcomas (STS). Consequently, the natural history and the clinical …
Prognostic factors and treatment outcomes of adult patients with rhabdomyosarcoma after multimodality treatment
YT Liu, CW Wang, RL Hong, SH Kuo - Anticancer Research, 2019 - ar.iiarjournals.org
Background: Adults with rhabdomyosarcoma (RMS) have a worse clinical outcome
compared to pediatric cases. In the present study, the failure pattern and clinical outcome of …
compared to pediatric cases. In the present study, the failure pattern and clinical outcome of …
Characteristics and prognosis of embryonal rhabdomyosarcoma in children and adolescents: An analysis of 464 cases from the SEER database
X Wang, J Feng, Z Li, X Zhang, J Chen… - Pediatric Investigation, 2020 - mednexus.org
Importance: As the most common subtype of pediatric rhabdomyosarcoma (RMS), the
prognosis of embryonal RMS has rarely been investigated solely. Objective: To perform a …
prognosis of embryonal RMS has rarely been investigated solely. Objective: To perform a …
[HTML][HTML] Embryonal rhabdomyosarcoma of the tongue in adults
A Díez-Montiel, R Antúnez-Conde, C Navarro Cuéllar… - Life, 2023 - mdpi.com
Simple Summary Rhabdomyosarcoma is the most common malignant soft tissue sarcoma in
childhood and adolescence, with one-third of cases occurring in the head and neck region …
childhood and adolescence, with one-third of cases occurring in the head and neck region …
[HTML][HTML] Adult head and neck rhabdomyosarcoma: radiotherapy-based treatment, outcomes, and predictors of survival
D Zhao, F Zhou, W Liu, Z Huang, X Xu, B Zheng, C Liu… - BMC cancer, 2024 - Springer
Background Adult head and neck rhabdomyosarcoma (HNRMS) is an exceptionally rare
malignancy, and there is a paucity of data and research dedicated to understanding its …
malignancy, and there is a paucity of data and research dedicated to understanding its …
Diagnosis and treatment of rhabdomyosarcomas
M Łomiak, T Świtaj, M Spałek… - Oncology in Clinical …, 2023 - journals.viamedica.pl
Rhabdomyosarcoma (RMS) is a soft tissue sarcoma. The primary tumor is most commonly
localized in the head and neck, the urogenital system, or the limbs. Classification by the …
localized in the head and neck, the urogenital system, or the limbs. Classification by the …
Embryonal rhabdomyosarcoma masquerading as a left vocal cord granuloma
S Linton, E Stapleton, S Penney… - BMJ Case Reports …, 2020 - casereports.bmj.com
Embryonal rhabdomyosarcoma (ERMS) of the larynx in adults is an extremely rare
diagnosis with insidious onset and progression. Only six reports (including this one) have …
diagnosis with insidious onset and progression. Only six reports (including this one) have …