Results 251 to 260 of about 80,703 (286)
Some of the next articles are maybe not open access.
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 V, Rao, C V, Satyanaryana
openaire +2 more sources
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 V, Rao, C V, Satyanaryana
openaire +2 more sources
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
openaire +2 more sources
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 +2 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.
Andrea, Stuart, Jayant, Radhakrishnan
openaire +2 more sources
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.
Andrea, Stuart, Jayant, Radhakrishnan
openaire +2 more sources
Seminars in Pediatric Surgery, 2016
Pediatric non-rhabdomyosarcoma soft tissue sarcomas (NRSTS) are a heterogeneous group encompassing more than 50 different histological diagnoses arising from primitive mesenchymal tissue. Together, they comprise about half the soft tissue sarcomas diagnosed in children and young adults.
Roshni, Dasgupta, David, Rodeberg
openaire +2 more sources
Pediatric non-rhabdomyosarcoma soft tissue sarcomas (NRSTS) are a heterogeneous group encompassing more than 50 different histological diagnoses arising from primitive mesenchymal tissue. Together, they comprise about half the soft tissue sarcomas diagnosed in children and young adults.
Roshni, Dasgupta, David, Rodeberg
openaire +2 more sources
Clinical Orthopaedics and Related Research, 1993
In children and young adults, rhabdomyosarcoma occurs with a frequency that is equal to or greater than that of all the other forms of soft-tissue sarcoma combined. Although the responsiveness of rhabdomyosarcoma to chemotherapy varies greatly among tumors with different primary sites and with different histologic features, the overall results of ...
openaire +2 more sources
In children and young adults, rhabdomyosarcoma occurs with a frequency that is equal to or greater than that of all the other forms of soft-tissue sarcoma combined. Although the responsiveness of rhabdomyosarcoma to chemotherapy varies greatly among tumors with different primary sites and with different histologic features, the overall results of ...
openaire +2 more sources
Parameningeal Rhabdomyosarcoma
Radiology, 1979The records of 27 patients with rhabdomyosarcoma involving the parameningeal area (nasopharynx, paranasal sinus, and middle ear) treated from 1961 to 1976 were reviewed. Due to the location of the primary tumor, radiation and chemotherapy were used but surgery was limited to simple biopsy.
R C, Chan, W W, Sutow, R D, Lindberg
openaire +2 more sources
The American Journal of Surgery, 1969
The care of patients with rhabdomyosarcoma has undergone significant change in the past decade. Careful staging and multidisciplinary treatment have improved the prognosis for patients with this neoplasm. A review of the medical literature of the past decade documents these changes in staging, therapy and prognosis.
openaire +3 more sources
The care of patients with rhabdomyosarcoma has undergone significant change in the past decade. Careful staging and multidisciplinary treatment have improved the prognosis for patients with this neoplasm. A review of the medical literature of the past decade documents these changes in staging, therapy and prognosis.
openaire +3 more sources
Genitourinary Rhabdomyosarcoma
Journal of Urology, 1983Rhabdomyosarcoma is the most common soft tissue malignant neoplasm involving the pelvis of children. Debate still exists over whether the best treatment is pelvic exenteration, radiation and chemotherapy or chemotherapy as the cornerstone to treatment, with diminished needs for extensive surgery and prolonged radiotherapy. Contrariwise, there is little
W E, Kaplan, C F, Firlit, R M, Berger
openaire +2 more sources
Urology, 1999
Rhabdomyosarcoma is a malignant tumor well known to urologists. These tumors arise from the genitourinary system in 20% to 25% of cases, most commonly from the bladder, prostate, vagina, and paratesticular region. This is the first reported case of a rhabdomyosarcoma arising from the ureter.
M F, Townsend +5 more
openaire +2 more sources
Rhabdomyosarcoma is a malignant tumor well known to urologists. These tumors arise from the genitourinary system in 20% to 25% of cases, most commonly from the bladder, prostate, vagina, and paratesticular region. This is the first reported case of a rhabdomyosarcoma arising from the ureter.
M F, Townsend +5 more
openaire +2 more sources