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HİPERFİBROTİK MİYELODİSPLASTİK SENDROM: İKİ OLGUNUN SUNUMU

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Abstract (2. Language): 
Hyperfibrotic Myelodisplastic Syndrome: Report of Two Cases: Myelodisplastic syndrome (MDS) is a heterogenous group of hematological disorders characterized by persistent cytope-nia in peripheral blood, dysplastic and ineffective hematopoiesis in bone marrow and an incre-ased risk of transformation to acute leukemia. Bone marrow fibrosis (myelofibrosis) may ac-company some MDS cases who had previous antineoplastic therapy, but extremely rare in unt-reated MDS cases. Here we report clinical, pathological and radiological characteristics of two hyperfibrotic MDS cases.
Abstract (Original Language): 
Myelodisplastik sendrom (MDS), çevre kanında sitopeniler, kemik iliğinde displastik ve ine-fektif eritropoez ile seyreden ve akut lösemiye dönüşüm riski olan heterojen bir grup hastalığın ortak adıdır. Antineoplastik tedavi alan MDS olgularında kemik iliğinde fibroz gelişebilir, ancak tedavi görmemiş olgularda ileri derecede fibroz oldukça nadirdir. Bu yazıda hiperfibro-tik MDS saptanan iki olgunun klinik, patolojik ve radyolojik bulguları sunulmaktadır.
310-315

REFERENCES

References: 

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