منابع مشابه
mammary sarcoma - not otherwise specified: a case report
mammary sarcomas are a heterogeneous group of malignant neoplasms that arise from the mammary stroma. primary sarcomas of the breast are extremely rare and comprise less than 0.1% of all malignant tumors of the breast. we present the case of a 56-year-old female diagnosed as stromal sarcoma, not otherwise specified - a very rare entity.
متن کاملPeripheral T-cell lymphoma, not otherwise specified
Peripheral T-cell lymphoma, not otherwise specified, is a broad category of biologically and clinically heterogeneous diseases, which can not be further classified into any other of the existing entities defined by the World Health Organization classification. Anthracycline-containing regimens, namely cyclophosphamide, doxorubicin, vincristine and prednisone (CHOP), nowadays represent the stand...
متن کاملPeripheral T-cell lymphoma, not otherwise specified
The peripheral T-cell lymphoma, not otherwise specified (PTCL, NOS) belongs to a heterogeneous class of aggressive neoplasms. Although several morphologic subtypes of this tumor have been described, no particular genetic, immunological, or distinct clinical features define this disease. Patients can experience night sweats, fever, lymphadenopathy, weight loss, splenomegaly, and/or skin changes....
متن کاملthe investigation of the relationship between type a and type b personalities and quality of translation
چکیده ندارد.
angiotensin ii type 1 receptor gene a1166c polymorphism was not associated with acute coronary syndrome in an iranian population
conclusions the at1r a1166c polymorphism appeared not to be associated with the presence of acs in the population studied. background there are very limited data for iranian populations on the predisposing genetic factors for acute coronary syndrome (acs). results there was no statistical difference in the genotype frequency of patients and healthy subjects with regard to age and gender (p > 0....
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ژورنال
عنوان ژورنال: BMJ
سال: 1995
ISSN: 0959-8138,1468-5833
DOI: 10.1136/bmj.310.6986.1070c