Recent Papers on Rhabdomyosarcoma – 04 February 2014
From Google Scholar Alerts
Please note that some are abstracts requiring subscriptions or purchase of the full article, others provide a more comprehensive view of the paper.
Pleomorphic rhabdomyosarcoma of the cerebellopontine angle in an adult: a review of literature
F Caporlingua, G Lapadula, M Antonelli, P Missori - BMJ Case Reports, 2014
Summary Rhabdomyosarcoma (RMS) is a rare and aggressive neoplasm characterised by
rapid growth and metastatic invasion. The most frequent localisation is the skeletal
musculature of the limbs. The head and the neck are rarely involved. A 50-year-old ...
Proliferative fasciitis mimicking a sarcoma in a child: A case report
K Yamaga, K Shomori, H Yamashita, K Endo… - The Journal of Dermatology, 2014
... Download figure to PowerPoint. Based on the clinical findings and imaging examination, we
diagnosed the tumor as malignant, such as rhabdomyosarcoma, synovial sarcoma or epithelioid
sarcoma (ES), or a pseudosarcomatous lesion, such as nodular fasciitis and PF. ...
Detection of Common Chromosomal Translocations by RT-PCR in a Mexican Cohort of Small Round Blue Cell Pediatric Tumors
MV Ponce-Castañeda, AJ García-Chéquer, PE Aguilar… - Archives of Medical …, 2014
... Identification of mRNA chimeras using RT-PCR discriminates among alveolar rhabdomyosarcoma
(ARMS), Ewing's sarcoma (ES/pPNET), synovial sarcoma (SS) and desmoplastic small round
cell tumor (DSRCT); however, frequencies of these translocations are variable. ...
Solid Tumors in the Neonatal Period
KS Fernández - NeoReviews, 2014
... Abbreviations: CMN; congenital mesoblastic nephroma CT; computed tomography HH; hepatic
hemangioma HVA; homovanillic acid IFS; infantile fibrosarcoma MRI; magnetic resonance imaging
RMS; rhabdomyosarcoma RTK; rhabdoid tumor of the kidney SCT ...
Childhood and adolescent cancer statistics, 2014
E Ward, C DeSantis, A Robbins, B Kohler, A Jemal - CA: A Cancer Journal for …, 2014
... Bone tumors, 49%, 73%. Osteosarcoma, 45%, 71%. Ewing sarcoma, 42%, 72%.
Rhabdomyosarcoma, 49%, 64%. Testicular germ cell tumors, 74%, 96%. ... Ewing sarcoma, 66%,
60%, 59%, 90%. Rhabdomyosarcoma, 65%, 62%, 61%, 90%. Testicular germ cell tumors, 94%, ...
Chemotherapy, Irradiation, and Surgery for Function-preserving Curative Therapy of Primary Extremity Soft Tissue Sarcomas: Initial Treatment With I-MAP and Inhalation GM-CSF During Preoperative Irradiation and Postoperatively
M Haddock, F Sim, MI O'Connor - 2014
... Patients were excluded from the study if they had a significant infection; active heart disease;
symptomatic pulmonary disease; had previous cancer chemo- therapy or irradiation; had
metastatic disease; had either embryonal rhabdomyosarcoma or extraosseous Ewing sar ...
Tumor Increase on MRI after Neoadjuvant Treatment is Associated with Greater Pathologic Necrosis and Poor Survival in Patients with Soft Tissue Sarcoma
M Bedi, J Kharofa, EV Zambrano, J Chang, K Baynes - J Integr Oncol, 2013
... Exclusion criteria included metastatic disease on initial presentation, STS of locations other than
the extremity or body- wall, recurrent sarcomas, and histopathologic types demonstrating
rhabdomyosarcoma, extraosseous primitive neuroectodermal tumor, Ewing's sarcoma ...
Pediatric Sclerosing Rhabdomyosarcomas: A Review
MC Amandeep Kumar, MC Manmohan Singh…
... some light on this possibly new subtype of RMS. Keywords: Sclerosing,
Rhabdomyosarcoma, Pediatric, Skull Base Page 3. Introduction Rhabdomyosarcoma
(RMS) is the commonest soft tissue tumor of childhood  with predilection ...