Results 31 to 40 of about 12,658 (224)
Oral Rhabdomyosarcoma: a review [PDF]
, 2012 Rhabdomyosarcoma (RMS) is a rare malignant soft tissue neoplasm comprised of cells derived from the primitive mesen¬chyme. About 35% of RMS arises in the head and neck, are are classified as parameningeal and non-parameningeal forms.
Sethi, Kanika +2 more
core +1 more source
Embryonal rhabdomyosarcoma of nasopharynx [PDF]
Indian Journal of Otolaryngology and Head & Neck Surgery, 1999 A rare case of Embryonal Rhabdomyosarcoma in a 5 year male child involving Nasopharynx with intracranial. secondaries is reported. The child presented with difficulty in breathing and swallowing with change of the voice and bleeding from nose and mouth off and on.
B S, Tuli, T L, Parmar
openaire +2 more sources
Multimodality imaging of vaginal rhabdomyosarcoma
Indian Journal of Radiology and Imaging, 2017 Rhabdomyosarcoma (RMS) is a malignant mesenchymal tumor arising from the embryonal muscle cells (rhabdomyoblasts), and is the most common soft tissue sarcoma in children and young adults accounting for 4–6% of all malignancies in this age group.
Richa S Chauhan +4 more
doaj +1 more source
Sensitivity to cdk1-inhibition is modulated by p53 status in preclinical models of embryonal tumors [PDF]
, 2015 Dysregulation of the cell cycle and cyclin-dependent kinases (cdks) is a hallmark of cancer cells. Intervention with cdk function is currently evaluated as a therapeutic option in many cancer types including neuroblastoma (NB), a common solid tumor of ...
Eggert, Angelika +8 more
core +2 more sources
Pediatric primary orbital rhabdomyosarcoma
Journal of Pediatric Surgery Case Reports, 2020 Introduction: Orbital rhabdomyosarcoma is the most common orbital malignancy of childhood, with approximately 4 or 5 new cases per year per million children younger under 20 years of age.
Ho Huu Thien +4 more
doaj +1 more source
Case Report: Pediatric Hepatic Rhabdomyosarcoma With Maximum Lifetime
Frontiers in Medicine, 2022 Primary intrahepatic rhabdomyosarcoma is an extremely rare malignant tumor. Here, we describe a case of embryonal rhabdomyosarcoma of the liver in a 7-year-old boy without any symptoms.
Xu Li +6 more
doaj +1 more source
Oral and Maxillofacial Surgery Cases, 2019 Rhabdomyosarcoma (RMS) is one of the most common soft tissue sarcomas encountered in paediatric patients. Embryonal rhabdomyosarcoma (ERMS), a variant of RMS, is observed in more than 70% of the cases and predominantly arises from head and neck region ...
Sohaib Shujaat +4 more
doaj +1 more source
Pharmacological targeting of the ephrin receptor kinase signalling by GLPG1790 in vitro and in vivo reverts oncophenotype, induces myogenic differentiation and radiosensitizes embryonal rhabdomyosarcoma cells [PDF]
, 2017 EPH (erythropoietin-producing hepatocellular) receptors are clinically relevant targets in several malignancies. This report describes the effects of GLPG1790, a new potent pan-EPH inhibitor, in human embryonal rhabdomyosarcoma (ERMS) cell ...
Beirinckx, Filip +20 more
core +3 more sources
Embryonal Rhabdomyosarcoma [PDF]
Oral Surgery, Oral Medicine, Oral Pathology and Oral Radiology, 2020 JOSÉ FRANCISCO TORRES ANGUIANO +6 more
+4 more sources
a report from the Children's Oncology Group and the Utah Population Database [PDF]
, 2015 Relatively little is known about the epidemiology and factors underlying susceptibility to childhood rhabdomyosarcoma (RMS). To better characterize genetic susceptibility to childhood RMS, we evaluated the role of family history of cancer using data from
Curtin, Karen +13 more
core +1 more source