t(11;22)(q24;q12) in rhabdomyosarcomas (RMS)
نویسندگان
چکیده
منابع مشابه
Dehydroretronecine-induced rhabdomyosarcomas in rats.
Two groups of rat were given s.c. injections of either monocrotaline or its major detectable metabolite, dehydroretronecine, biweekly for 1 year. Tissues obtained from partial hepatectomies performed at 4 months on a portion of these animals showed that both compounds caused a decided inhibition of mitotic division in regenerating liver. Rhabdomyosarcomas developed at the site of dehydroretrone...
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Rhabdomyosarcomas (RSCs) are skeletal muscle neoplasms found in humans and domestic mammals. The A/J inbred strain developed a high frequency (between 70-80%) of adult pleomorphic type (APT) RSC at >20 months of age while BALB/cByJ also develop RSC but less frequently. These neoplasms invaded skeletal muscle surrounding either the axial or proximal appendicular skeleton and were characterized b...
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When six rhabdomyosarcomas were stained with antisera by the fluorescein label technic, three (classified as embryonal and usually difficult to diagnose as rhabdomyosarcoma) appeared to contain myosin, since they reacted with antimyosin antibody, whereas the remaining three, which were easier to classify as typical rhabdomyosarcoma histologically, appeared to contain no myosin. Anticonnective t...
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Sclerosing RMS (SRMS) is a recently described subtype of RMS that has not yet been included in any of the classification systems for RMSs. We did pubmed search using keywords "sclerosing, and rhabdomyosarcomas" and included all pediatric cases (age ≤ 18 years) of SRMSs in this review. We also included our case of an eleven-year-old male child with skull base SRMS and discuss the clinical, histo...
متن کاملMyogenin and MyoD1 expression in paediatric rhabdomyosarcomas.
The diagnosis of paediatric solid tumours is often based on small tissue needle biopsies in which many different entities demonstrate a "small round cell tumour" phenotype and in which there may be insufficient tissue to allow the interpretation of diagnostic architectural features, which may be present in larger specimens. Therefore, the extensive use of a panel of immunohistochemical markers ...
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ژورنال
عنوان ژورنال: Atlas of Genetics and Cytogenetics in Oncology and Haematology
سال: 2011
ISSN: 1768-3262
DOI: 10.4267/2042/44990