Results 11 to 20 of about 54,150 (267)

Paratesticular spindle cell rhabdomyosarcoma

open access: yesRare Tumors, 2015
Spindle cell rhabdomyosarcoma is a rare variant of embryonal rhabdomyosarcoma that affects young males and most commonly involves the paratesticular region.
Biswajit Dey   +5 more
doaj   +2 more sources

Rhabdomyosarcoma of the kidney

open access: yesJournal of Pediatric Surgery Case Reports, 2018
Rhabdomyosarcoma is considered the most common soft tissue sarcoma arising in patients younger than 15 years old, accounting for 5%–10% of childhood solid tumors. Sarcoma of the kidney represents 1% of all primary renal malignancies.
Alaa Samkari, Haneen Al-Maghrabi
doaj   +2 more sources

Efficient lysis of rhabdomyosarcoma cells by cytokine-induced killer cells: implications for adoptive immunotherapy after allogeneic stem cell transplantation [PDF]

open access: yesHaematologica, 2010
Background Rhabdomyosarcoma is the most common soft tissue sarcoma in childhood and has a poor prognosis. Here we assessed the capability of ex vivo expanded cytokine-induced killer cells to lyse both alveolar and embryonic rhabdomyosarcoma cell lines ...
Selim Kuçi   +12 more
doaj   +2 more sources

Rhabdomyosarcoma-Induced Uterine Inversion

open access: yesCase Reports in Obstetrics and Gynecology, 2022
Nonpuerperal uterine inversion is a rare clinical condition that involves prolapse of the uterine fundus into the uterine cavity and vaginal vault and possibly passed the introitus.
Kin Li   +3 more
doaj   +2 more sources

Pleomorphic rhabdomyosarcoma in adults: a case report

open access: yesJournal of Medical Case Reports
Background Rhabdomyosarcoma is a rare type of soft-tissue sarcoma that is more frequently observed in children and is less common in adults. Rhabdomyosarcoma can occur in any part of the body, including tissues without skeletal muscles. The main subtypes
Zahra Aminparast   +2 more
doaj   +2 more sources

Rhabdomyosarcoma [PDF]

open access: yesNature Reviews Disease Primers, 2019
Rhabdomyosarcoma (RMS) is the most common soft tissue sarcoma in children and represents a high-grade neoplasm of skeletal myoblast-like cells. Decades of clinical and basic research have gradually improved our understanding of the pathophysiology of RMS and helped to optimize clinical care.
Stephen X, Skapek   +7 more
  +8 more sources

Rhabdomyosarcoma [PDF]

open access: yesPediatric Blood & Cancer, 2021
AbstractRhabdomyosarcoma is a heterogeneous disease both in presentation and histology. Improvements in a multimodality therapy resulted in the improved overall survival for patients with a low‐risk and intermediate‐risk disease but not for patients with a metastatic disease. We reviewed and contrasted the North American and European practice patterns,
Yechieli, Raphael L.   +10 more
openaire   +2 more sources

Characteristic of Uterine Rhabdomyosarcoma by Algorithm of Potential Biomarkers for Uterine Mesenchymal Tumor

open access: yesCurrent Oncology, 2022
Background/Aim: Patients with uterine sarcoma comprise 2–5% of all patients with uterine malignancies; however, the morbidity of uterine sarcoma is low compared with that of other gynecological cancers.
Saya Tamura   +5 more
doaj   +1 more source

MYBPC2 and MYL1 as Significant Gene Markers for Rhabdomyosarcoma

open access: yesTechnology in Cancer Research & Treatment, 2021
Background: Rhabdomyosarcoma is the most common soft tissue tumor in children. Rhabdomyosarcoma commonly results in pain and bleeding caused by tumor compression and is prone to early metastasis and recurrence, which can seriously affect the therapeutic ...
Zihang Chen MS   +3 more
doaj   +1 more source

Femoral intraosseous rhabdomyosarcoma: a case report and literature review

open access: yesBrazilian Journal of Oncology, 2021
Introduction: Rhabdomyosarcoma is the most common soft tissue sarcoma in childhood. However, primary bone rhabdomyosarcoma is a rare entity with some few cases reported. Case Report: We present a case of a 19-year-old female patient referred
Dan Carai Maia Viola   +6 more
doaj   +1 more source

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