Results 221 to 230 of about 54,150 (267)
Some of the next articles are maybe not open access.
PARATESTICULAR RHABDOMYOSARCOMA
Acta Pathologica Japonica, 1983Two cases of paratesticular rhabdomyosarcoma were reported. One was a 53‐year‐old male, who was admitted to the Hospital because of swelling of the scrotum, hemosputa, and complete left hemiplegia. Clinical diagnosis was testicular tumor with remote metastases to lung, brain, liver, and paraaortic lymph nodes.
M, Kage +4 more
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
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
2016
In vivo models of Rhabdomyosarcoma (RMS) have proven instrumental in understanding the development and progression of this devastating pediatric sarcoma. Both vertebrate and invertebrate model systems have been developed to study the tumor biology of both embryonal (ERMS) and alveolar (ARMS) RMS subtypes.
Michael, Phelps, Eleanor, Chen
openaire +2 more sources
In vivo models of Rhabdomyosarcoma (RMS) have proven instrumental in understanding the development and progression of this devastating pediatric sarcoma. Both vertebrate and invertebrate model systems have been developed to study the tumor biology of both embryonal (ERMS) and alveolar (ARMS) RMS subtypes.
Michael, Phelps, Eleanor, Chen
openaire +2 more sources
Seminars in Pediatric Surgery, 2012
Rhabdomyosarcoma (RMS) is a malignant childhood tumor of mesenchymal origin that currently has a greater than 70% overall 5-year survival. Multimodality treatment is determined by risk stratification according to pretreatment stage, postoperative group, histology, and site of the primary tumor.
Roshni, Dasgupta, David A, Rodeberg
openaire +2 more sources
Rhabdomyosarcoma (RMS) is a malignant childhood tumor of mesenchymal origin that currently has a greater than 70% overall 5-year survival. Multimodality treatment is determined by risk stratification according to pretreatment stage, postoperative group, histology, and site of the primary tumor.
Roshni, Dasgupta, David A, Rodeberg
openaire +2 more sources
Topics in Companion Animal Medicine
A geriatric Holland Lop rabbit presented for acute lameness. A pathologic fracture of the right distal femur associated with a pleomorphic rhabdomyosarcoma was diagnosed, and staging radiographs showed no overt metastasis upon initial presentation. The limb was amputated and submitted for microscopic examination. Immunohistochemical evaluation revealed
Logan Kopp, Michael Garner, Kara Priest
openaire +2 more sources
A geriatric Holland Lop rabbit presented for acute lameness. A pathologic fracture of the right distal femur associated with a pleomorphic rhabdomyosarcoma was diagnosed, and staging radiographs showed no overt metastasis upon initial presentation. The limb was amputated and submitted for microscopic examination. Immunohistochemical evaluation revealed
Logan Kopp, Michael Garner, Kara Priest
openaire +2 more sources
The Ultrastructure of Rhabdomyosarcoma
American Journal of Clinical Pathology, 1970The ultrastructural features of one embryonal and two pleomorphic rhabdomyosarcomas in adults are described. The presence of thick myofilaments in formations suggesting sarcomeres and a rare arrangement of mitochondria in tandem allow for identification of the spindle cells in embryonal rhabdomyosarcoma as skeletal muscle cells.
B L, Horvat, M, Caines, E R, Fisher
openaire +2 more sources
Rhabdomyosarcoma of the larynx
The Journal of Laryngology & Otology, 1975A case of rhabdomyosarcoma of the larynx in a 54-year-old man is reported. Patient presented dramatically with a large tumour mass obstructing his laryngeal inlet. The patient remains alive and well sixteen months after a total laryngectomy. Only seven previous reports of a rhabdomyosarcoma of the larynx could be found in the literature and these are ...
openaire +2 more sources