Results 21 to 30 of about 99,358 (330)

Chorein sensitive microtubule organization in tumor cells [PDF]

PeerJ, 2023
Background The purpose of this study is to analyzed the involvement of chorein in microtubules organization of three types of malignant; rhabdomyosarcoma tumor cells (ZF), rhabdomyosarcoma cells (RH30), and rhabdomyosarcoma cells (RD).
Saad Alkahtani, Abdullah A. Alkahtane, Christos Stournaras, Saud Alarifi   +3 more
doaj   +2 more sources

Surgical management of paratesticular rhabdomyosarcoma: A consensus opinion from the Children's Oncology Group, European paediatric Soft tissue sarcoma Study Group, and the Cooperative Weichteilsarkom Studiengruppe

Pediatric Blood & Cancer, 2021
The treatment of paratesticular rhabdomyosarcoma (PT‐RMS) has varied over time and by cooperative group. The International Soft Tissue Sarcoma Database Consortium (INSTRuCT) is a collaboration of the Children's Oncology Group (COG) Soft Tissue Sarcoma ...
T. Rogers, G. Seitz, J. Fuchs, H. Martelli, R. Dasgupta, J. Routh, D. Hawkins, E. Koscielniak, G. Bisogno, D. Rodeberg   +9 more
semanticscholar   +1 more source

Facial Pain as the Initial Presentation of Rhabdomyosarcoma: A Case Report. [PDF]

Clin Case Rep
ABSTRACT Spindle cell/sclerosing rhabdomyosarcoma (RMS) is an uncommon and aggressive neoplasm, especially in adults. This case details a 35‐year‐old male with a 4‐year history of persistent idiopathic facial pain (PIFP), first misdiagnosed owing to the lack of definitive clinical or radiologic evidence.
Anbiaee N, Pakfetrat A, Yousefi S, Saghravanian N, Salari S.   +4 more
europepmc   +2 more sources

Tumor response and endogenous immune reactivity after administration of HER2 CAR T cells in a child with metastatic rhabdomyosarcoma

Nature Communications, 2020
Refractory metastatic rhabdomyosarcoma is largely incurable. Here we analyze the response of a child with refractory bone marrow metastatic rhabdomyosarcoma to autologous HER2 CAR T cells.
M. Hegde, S. Joseph, F. Pashankar, C. Derenzo, Khaled Sanber, Shoba A. Navai, Tiara T. Byrd, J. Hicks, Mina L. Xu, C. Gerken, M. Kalra, C. Robertson, Huimin Zhang, Ankita Shree, B. Mehta, O. Dakhova, V. Salsman, B. Grilley, A. Gee, G. Dotti, H. Heslop, M. Brenner, W. Wels, S. Gottschalk, N. Ahmed   +24 more
semanticscholar   +1 more source

Proton beam therapy in paediatric cancer: Anticipating the opening of the Australian Bragg Centre for Proton Therapy and Research

Journal of Medical Imaging and Radiation Oncology, EarlyView., 2023
Summary Proton Beam Therapy (PBT) has the potential to improve paediatric cancer care by reducing radiation exposure and thus long‐term toxicities. Ethical concerns and debates surrounding the treatment, such as eligibility and accessibility, are ongoing in Australia. The Australian Bragg Centre for Proton Therapy and Research (ABCPTR) (named after Sir
Jeremy Khong, Hui Tee, Peter Gorayski, Hien Le, Michael Penniment, Sophie Jessop, Jordan Hansford, Melanie Penfold, Julia Green, Kelly Skelton, Frank Saran   +10 more
wiley   +1 more source

Embryonal Rhabdomyosarcoma of Prostate in Adult: A Rare Case Report

Folia Medica Indonesiana, 2021
Rhabdomyosarcoma is the fifth most common type of soft tissue solid tumor in children and the most common in the last two decades. Rhabdomyosarcoma of the urogenital organ is a rare mesenchymal tumor, covering 22% of all Rhabdomyosarcoma cases.
Dimas Panca Andhika, Sunaryo Hardjowijoto   +1 more
doaj   +1 more source

BLADDER EMBRYONAL RHABDOMYOSARCOMA IN AN 18-MONTHS-OLD BOY: A CASE REPORT

Jurnal Urologi Indonesia, 2023
Objective: This study aims to report a case of bladder embryonal rhabdomyosarcoma in an 18-months-old boy. Case(s) Presentation: An 18-months-old boy presented with complaint of difficult urinating since the last 2 months before presentation.
I Made Mahandita, Besut Daryanto, Pradana Nurhadi   +2 more
doaj   +1 more source

Association of Ataxia Telangiectasia Mutated (ATM) gene mutation/deletion with Rhabdomyosarcoma

Molecular Cancer, 2003
Background Rhabdomyosarcoma is a common malignancy in children. There are two major types of rhabdomyosarcomas, the embryonal and the alveolar, differing in cytogenetic and morphologic features.
Feramisco James R, Newbury Robert O, Puri Pier, Bhakta Kunjan S, Zhang Peilin, Wang Jean Y   +5 more
doaj   +1 more source

Rhabdomyosarcoma: Advances in Molecular and Cellular Biology. [PDF]

, 2015
Rhabdomyosarcoma (RMS) is the most common soft tissue malignancy in childhood and adolescence. The two major histological subtypes of RMS are alveolar RMS, driven by the fusion protein PAX3-FKHR or PAX7-FKHR, and embryonic RMS, which is usually ...
Duan, Zhenfeng, Guo, Wei, Hornicek, Francis J, Mankin, Henry J, Shen, Jacson K, Sun, Xin   +5 more
core   +3 more sources

Metastatic Alveolar Rhabdomyosarcoma with Extensive Bone Marrow Replacement in an Older Adult

Case Reports in Oncology, 2021
Rhabdomyosarcoma is extremely rare in adults. Metastatic rhabdomyosarcoma can resemble other malignancies, which can delay diagnosis and prompt treatment.
Justin J. Cheng, Ryan T. Mott, Paul D. Savage, Ravi K. Paluri   +3 more
doaj   +1 more source