Results 81 to 90 of about 99,358 (330)
The Case for Primary Salivary Rhabdomyosarcoma
Frontiers in Oncology, 2015 Rhabdomyosarcomas of the parotid and submandibular glands have the histological appearance of a skeletal muscle tumor yet can be found in tissue with no striated muscular elements. We examine the potential cell-of-origin for rhabdomyosarcoma and whether
Mathew eGeltzeiler +4 more
doaj +1 more source
Inhibition of lipid metabolism exerts antitumor effects on rhabdomyosarcoma
Cancer Medicine, 2021 Rhabdomyosarcoma exhibits tumor‐specific energy metabolic changes that include the Warburg effect. Since targeting cancer metabolism is a promising therapeutic approach, we examined the antitumor effects of suppressing lipid metabolism in ...
Satoshi Miyagaki +5 more
doaj +1 more source
Acta Neuropathologica, 2018 Patients with DICER1 predisposition syndrome have an increased risk to develop pleuropulmonary blastoma, cystic nephroma, embryonal rhabdomyosarcoma, and several other rare tumor entities.
C. Koelsche +32 more
semanticscholar +1 more source
Laparoscopic Partial Cystectomy for Inflammatory Myofibroblastic Tumor of the Urinary Bladder
IJU Case Reports, EarlyView.ABSTRACT Introduction Inflammatory myofibroblastic tumor (IMT) of the bladder is a rare benign tumor characterized by atypical spindle cell proliferation and inflammatory cell infiltration, typically involving lymphocytes and plasma cells. Case Presentation A 38‐year‐old woman presented with micturition pain and urinary frequency.
Hajime Yamasaki +8 more
wiley +1 more source
The role of midfacial degloving in modern rhinological practice [PDF]
, 1999 The midfacial degloving approach has been available for twenty five years and is slowly increasing in popularity in the management of extensive benign lesions of the sinonasal region, for selected malignancy in this area and to afford access to the ...
Howard, DJ, Lund, VJ
core +1 more source
Insights into pediatric rhabdomyosarcoma research: Challenges and goals
Pediatric Blood & Cancer, 2019 Overall survival rates for pediatric patients with high‐risk or relapsed rhabdomyosarcoma (RMS) have not improved significantly since the 1980s. Recent studies have identified a number of targetable vulnerabilities in RMS, but these discoveries have ...
M. Yohe +32 more
semanticscholar +1 more source
Journal of Medical Radiation Sciences, EarlyView.Contouring organs at risk (OARs) manually in paediatric patients undergoing cranial‐spinal radiation therapy (CSI) is a time‐consuming, labour‐intensive task. This study aims to assess the accuracy and clinical acceptability of auto‐contours produced by the Siemens DirectORGANS auto‐contouring software on paediatric patients receiving CSI treatment ...
Isabel Cant +6 more
wiley +1 more source
Congenital Rhabdomyosarcoma Presenting as a Neck Mass at Birth
Case Reports in Pediatrics, 2018 Rhabdomyosarcoma is a malignant tumor of the soft tissues which preferentially affects the pediatric population. Neonatal rhabdomyosarcoma is rare, and much of the published literature concerning this entity consists of isolated case reports and small ...
Leah E. Waldman +3 more
doaj +1 more source
Temozolomide combined with irinotecan caused regression in an adult pleomorphic rhabdomyosarcoma patient-derived orthotopic xenograft (PDOX) nude-mouse model. [PDF]
, 2017 Adult pleomorphic rhabdomyosarcoma (RMS) is a rare and recalcitrant, highly-malignant mesenchymal tumor in need of improved therapeutic strategies.
Dry, Sarah M +14 more
core +1 more source
Rhabdomyosarcoma of nasopharynx [PDF]
Indian Journal of Otolaryngology and Head & Neck Surgery, 1999 Rhabdomyosarcoma is a highly invasive malignant tumour arising from the mesenchymal tissue. Here, we reported a rare case of embryonal rhadomyosarcoma of nasopharynx with extension to different spaces of base of skull and orbit. Rarity of the case difficulty in diagnosis encourages its reporting.
Sudip Kumar Das +4 more
openaire +3 more sources