How To Use Myosarcoma In A Sentence
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Sometimes very high doses of chemotherapyare necessary to wipe out rhabdomyosarcoma tumors that have become resistant to standard doses.
Rhabdomyosarcoma
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Abstract Objective To analyze the clinical characteristics of the childhood rhabdomyosarcoma.
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Although the study focused on patients with sarcomas such as rhabdomyosarcoma and Ewing sarcoma, Spunt said the results will likely change neutropenia treatment for all childhood cancer patients get growth factor support during their therapy, "Spunt explained.
THE MEDICAL NEWS
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Bone marrow transplantationis another type of treatment that is being studied for recurrent rhabdomyosarcoma.
Rhabdomyosarcoma
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One case each of leiomyosarcoma involved the bladder and kidney and had been treated by partial cystectomy and total nephrectomy, respectively.
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The cancer - rhabdomyosarcoma - has only been seen in two other cases in the world.
The Sun
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Michael died from rhabdomyosarcoma, also known as desmoplastic soft tissue sarcoma.
East Brunswick Sentinel
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Intracranial rhabdomyosarcomas are rare neoplasms, and those thought to be primary meningeal tumors are even more rare.
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David was diagnosed in May 2003 with a grapefruit-sized malignant brain tumour called a rhabdomyosarcoma, which was causing blindness and headaches.
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How do we diagnose rhabdomyosarcoma in your child?
Rhabdomyosarcoma
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Opponents of BNL pointed out that levels of soft tissue cancers and rare diseases such as rhabdomyosarcoma were extraordinarily higher adjacent to the water recharge area near the lab.
The Full Feed from HuffingtonPost.com
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Histologically, the tumor was composed of two distinct components - an epithelioid component with granular cytoplasm that stained for synaptophysin, melan-A, calretinin, and vimentin compatible with adrenocortical differentiation, and a pleomorphic to spindled component that was positive for desmin and myogenin, compatible with rhabdomyosarcomatous differentiation.
BioMed Central - Latest articles
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In collaboration with Dr. Barr, who discovered the gene involved in alveolar rhabdomyosarcoma, Dr. Womer and others have used the chromosomal changes in sarcomas to determine response to treatment.
Pediatric cancer research
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Less likely is neuroblastoma, rhabdomyosarcoma and teratoma which would be more heterogenous when this size.
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One half of these malignancies are rhabdomyosarcomas originating in striated muscle.
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Usually, leiomyosarcomas originate from the renal capsule, muscle fibers in the renal pelvis, or the walls of renal vessels.
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Objective To study the effects of retinoic acid on the differentiation of human rhabdomyosarcoma cells and on the expression of myogenic regulatory factor (MRF).
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Small cell carcinomas are mainly misdiagnosed as other small round cell tumors (eg, neuroblastoma, Ewing sarcoma, embryonal rhabdomyosarcoma, lymphoma).
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Surgery is the most common treatment for rhabdomyosarcoma.
Rhabdomyosarcoma
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Equally unclear is the histogenesis of intracranial sarcomas and particularly rhabdomyosarcomas.
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Abstract: Objective : To improve the understanding and diagnosis of embryonal rhabdomyosarcoma of biliary tree in childhood.
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Usually, leiomyosarcomas originate from the renal capsule, muscle fibers in the renal pelvis, or the walls of renal vessels.
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What are the signs and symptoms of rhabdomyosarcoma?
Rhabdomyosarcoma
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The characteristic ‘organoid’ pattern helps distinguish fibrous hamartoma of infancy from rhabdomyosarcoma and from infantile fibrosarcomas.
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Other cancers -- In rare cases, patients with nevoid basal cell carcinoma syndrome (NBCCS) develop other cancers, such as rhabdomyosarcoma and Wilms’ tumor (cancer of the kidneys)
Nevoid Basal Cell Carcinoma Syndrome
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It's called rhabdomyosarcoma, a rare soft tissue cancer.
AARP.org :
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Objective : To improve the understanding and diagnosis of embryonal rhabdomyosarcoma of biliary tree in childhood.
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But early diagnosis is important, because rhabdomyosarcoma spreads quickly.
Rhabdomyosarcoma
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One half of these malignancies are rhabdomyosarcomas originating in striated muscle.
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Pleomorphic rhabdomyosarcomas have more uniform, deeply eosinophilic cytoplasm and display cell-to-cell molding and cross-striations by light microscopy.
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Rational Review
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Histologically, the tumor was composed of two distinct components - an epithelioid component with granular cytoplasm that stained for synaptophysin, melan-A, calretinin, and vimentin compatible with adrenocortical differentiation, and a pleomorphic to spindled component that was positive for desmin and myogenin, compatible with rhabdomyosarcomatous differentiation.
BioMed Central - Latest articles