Results 101 to 110 of about 12,658 (224)
Embryonal rhabdomyosarcoma of the cervix
Embryonal rhabdomyosarcoma (sarcoma botyroides) of the cervix, which is rare, is described in a 16-year-old. The combined use of chemotherapy, radiotherapy and surgery has markedly improved survival in those with this condition. However, our patient did not benefit from this treatment modality due to late presentation and loss to follow-up.
Ocheke A +4 more
openaire +4 more sources
Enhancer of zeste homolog 2 (EZH2) in pediatric soft tissue sarcomas: first implications. [PDF]
Soft tissue sarcomas of childhood are a group of heterogeneous tumors thought to be derived from mesenchymal stem cells. Surgical resection is effective only in about 50% of cases and resistance to conventional chemotherapy is often responsible for ...
CIARAPICA R +4 more
core +1 more source
From benign to malignant: Spectrum of skeletal muscle tumors in pediatric patients – A case series
Objectives: To demonstrate the biological spectrum of pediatric skeletal muscle tumors by presenting cases of fetal-type rhabdomyoma and embryonal rhabdomyosarcoma.
Sonali Goyal, Sunita Gupta, Sujoy Ghosh
doaj +1 more source
Multimodality management of soft tissue sarcomas [PDF]
Soft tissue sarcomas are a heterogeneous group of malignant tumours arising from connective tissues of mesenchymal origin. By definition sarcomas arising from bone or cartilage are excluded though they have much in common in their behaviour as well as in
Brincat, Stephen
core
Li-Ying Tang,1 Mou-Xin Zhang,2 Di-Han Lu,3 Yong-Xiong Chen,1 Zu-Guo Liu,1,2 San-Gang Wu4 1Eye Institute of Xiamen University, Fujian Provincial Key Laboratory of Ophthalmology and Visual Science, Medical College, Xiamen University, Xiamen 361005, People ...
Tang LY +5 more
doaj
The Impact of Age on Outcome of Embryonal and Alveolar Rhabdomyosarcoma Patients.:A Multicenter Study [PDF]
Background: The prognosis of rhabdomyosarcoma (RMS) in children and adolescents has improved since the introduction of multi-agent chemotherapy. However, outcome data of adults with RMS are scarce.
De Bont, Evelne S. J. M. +9 more
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Orbital Embryonal Rhabdomyosarcomain Karachi (1998-2002) [PDF]
Objective: To study the epidemiology of ocular Rhabdomyosarcoma (ORMS) in Karachi. Methods: Incident ORMS cases resident of Karachi, registered at Karachi Cancer Registry (KCR) during 1st January 1998 to 31st December 2002 were included in the study. The
Ahmed, R. +10 more
core +1 more source
Background Paratesticular rhabdomyosarcoma is an uncommon tumor, particularly in adults. While most cases of embryonal variant are diagnosed in children, adult presentation is sporadic and carries a worse prognosis.
Ahmed Mohammed Umar +4 more
doaj +1 more source
Integrating the diagnosis of childhood malignancies [PDF]
Significant progress has been made in understanding the molecular basis of pediatric malignancies. Mechanisms of pediatric acute leukemia induction include hyperdiploidy, aberrant expression of proto-oncogenes, and activation of transcription factors or ...
Lopez-Terrada, Dolores
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Genomic Profiling of Childhood Tumor Patient-Derived Xenograft Models to Enable Rational Clinical Trial Design. [PDF]
Accelerating cures for children with cancer remains an immediate challenge as a result of extensive oncogenic heterogeneity between and within histologies, distinct molecular mechanisms evolving between diagnosis and relapsed disease, and limited ...
Baxter, Patricia +68 more
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