Pregled bibliografske jedinice broj: 55477
Chromosome abnormalities of small round cell tumors
Chromosome abnormalities of small round cell tumors // Cytogenetics Cell Genetics / European Cytogeneticists Association (ur.).
Basel: S. Karger, 1999. str. 129-129 (poster, međunarodna recenzija, sažetak, znanstveni)
CROSBI ID: 55477 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Chromosome abnormalities of small round cell tumors
Autori
Petković, Iskra ; Ćepulić, Mladen ; Konja, Josip
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni
Izvornik
Cytogenetics Cell Genetics
/ European Cytogeneticists Association - Basel : S. Karger, 1999, 129-129
Skup
Second European Cytogenetic Conference
Mjesto i datum
Beč, Austrija, 03.07.1999. - 06.07.1999
Vrsta sudjelovanja
Poster
Vrsta recenzije
Međunarodna recenzija
Ključne riječi
Cytogenetics; Children; Solid tumors
Sažetak
During last twenty years considerable progress has been achieved in the field of cytogenetics of malignant diseases. Specific clonal cheomosomal abnormalities have been of practical value for the precise diagnosis and determination of prognosis. Investigation carried out so far have mostly dealt with hemoblastosis, whereas studies in children with solid tumors and lymphomas are rare. Small round (SRCT) is a heterogenous group of disease that include Ewing sarcoma, neuroblastoma, rhabdomyosarcoma and non-Hodgkin lymphoma. Due to similar histology this group of diseases is the most serious diagnostic probleme. The precise diagnosis is of particular importance since for different type of disease differing therapy is needed. In this study we present the results of cytogenetic analysis in 30 children with SCCT. The aim of this investigation is to determine the frequency and type of chromosome abnormalities, and evaluate the feasibility of cytogenetic analysis in differential diagnosis and prognosis. Cytogenetic analysis revealed clonal chromosomal abnormalities in 70% of children. The analysis revealed nonrandom involvement of chromosomal types in numerical and structural aberrations. This investigation confirms the diagnostic importance of cytogenetic investigations in SRCT of children.
Izvorni jezik
Engleski
Znanstvena područja
Kliničke medicinske znanosti
POVEZANOST RADA
Ustanove:
Klinika za dječje bolesti Medicinskog fakulteta,
Medicinski fakultet, Zagreb