Results 161 to 170 of about 40,129 (195)
Unveiling the Uncommon: Ewing Sarcoma Cranium - A Rare Clinical Vignette. [PDF]
J Orthop Case RepSharma K, Kumar S, Gupta R.
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Skull Base Rhabdomyosarcoma Mimicking Osteomyelitis in a Pediatric Patient. [PDF]
J Neurol Surg RepAdelman A +4 more
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Vaginal botryoid rhabdomyosarcoma in an infant: A case report and review of the literature. [PDF]
Radiol Case RepEssetti S +7 more
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Successful treatment of rare case of rhabdomyosarcoma of urinary bladder in adult, experience from tertiary hospital. Case report. [PDF]
Int J Surg Case RepChiloleti G +4 more
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Imaging Insights Suggesting a Sinister Cause of a Breast Mass in Adolescents: A Case of Rhabdomyosarcoma in a Teenager. [PDF]
Eur J Case Rep Intern MedMalik M +6 more
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Soft Tissue Sarcoma in Sub-Saharan Africa: Surgical Management Outcomes, Gaps, and Future Prospects: A Narrative Review. [PDF]
Health Sci RepAdebusoye FT +12 more
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The Indian Journal of Pediatrics, 1977
Six cases of rhabdomyosarcoma have been reported. Three of them were in the bladder, one in the tongue, one in the gluteal region and one in the leg muscles. The leg tumour was successfully treated by combined triple regimen of surgery, deep-X-ray therapy and D-Actinomycin.
T. Viswanatha Rao, C. V. Satyanaryana
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Six cases of rhabdomyosarcoma have been reported. Three of them were in the bladder, one in the tongue, one in the gluteal region and one in the leg muscles. The leg tumour was successfully treated by combined triple regimen of surgery, deep-X-ray therapy and D-Actinomycin.
T. Viswanatha Rao, C. V. Satyanaryana
openaire +3 more sources
The Indian Journal of Pediatrics, 2004
Rhabdomyosarcoma, the most common soft tissue sarcoma of children, carried a 10-15% survival rate in the late 1960s. Since then, better understanding of biology and pathology of the tumor and the judicious use of chemotherapy and radiation has improved the prognosis drastically.
Jayant Radhakrishnan, Andrea L. Stuart
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Rhabdomyosarcoma, the most common soft tissue sarcoma of children, carried a 10-15% survival rate in the late 1960s. Since then, better understanding of biology and pathology of the tumor and the judicious use of chemotherapy and radiation has improved the prognosis drastically.
Jayant Radhakrishnan, Andrea L. Stuart
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Seminars in Pediatric Surgery, 2016
A malignant tumor of striated muscle origin, rhabdomyosarcoma (RMS) is a childhood tumor that has benefited from nearly 30 years of multimodality therapy, culminating in a >70% overall 5-year survival. Prognosis for RMS is dependent on primary tumor site, age, completeness of resection, presence and number of metastatic sites, histology, and biology of
Roshni, Dasgupta +2 more
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A malignant tumor of striated muscle origin, rhabdomyosarcoma (RMS) is a childhood tumor that has benefited from nearly 30 years of multimodality therapy, culminating in a >70% overall 5-year survival. Prognosis for RMS is dependent on primary tumor site, age, completeness of resection, presence and number of metastatic sites, histology, and biology of
Roshni, Dasgupta +2 more
openaire +3 more sources