dc.contributor.author | Yilmaz Aksoy, Sabire | |
dc.contributor.author | Halac, Metin | |
dc.date.accessioned | 2021-03-03T15:19:11Z | |
dc.date.available | 2021-03-03T15:19:11Z | |
dc.date.issued | 2015 | |
dc.identifier.citation | Yilmaz Aksoy S., Halac M., "FDG PET/CT in pediatric Hodgkin's lymphoma", TURK ONKOLOJI DERGISI-TURKISH JOURNAL OF ONCOLOGY, cilt.30, sa.4, ss.240-251, 2015 | |
dc.identifier.other | vv_1032021 | |
dc.identifier.other | av_3e5d3b9b-ca99-4e56-a454-bfecd9656b98 | |
dc.identifier.uri | http://hdl.handle.net/20.500.12627/45788 | |
dc.identifier.uri | https://doi.org/10.5505/tjoncol.2015.1218 | |
dc.description.abstract | The increased glucose metabolism results increased 18F-Fluorodeoxyglucose (FDG) accumulation of the malignant cells. Similarly, Hodgkin's lymphoma (HL) show high FDG uptake. Lymphocyte-predominant types of HL demonstrate lower FDG accumulation than classic type HL. PET/CT can detect almost all lesion greater than 0.5-1 cm. Additionally, FDG PET/CT help us in monitoring treatment response by showing glucose metabolism and FDG uptake of the cells after chemotherapy. The sensitivity of FDG PET/CT is higher than other imaging modalities in detecting nodular or diffuse lesions of HL. Also, it has higher sensitivity in showing bone marrow involvement than bone marrow biopsy. As a result, FDG PET/CT is a widely accepted and superior imaging modality in staging, re-staging and evaluating treatment response of pediatric HL. | |
dc.language.iso | eng | |
dc.subject | Onkoloji | |
dc.subject | Sağlık Bilimleri | |
dc.subject | İç Hastalıkları | |
dc.subject | Dahili Tıp Bilimleri | |
dc.subject | Tıp | |
dc.subject | Klinik Tıp (MED) | |
dc.subject | Klinik Tıp | |
dc.subject | ONKOLOJİ | |
dc.title | FDG PET/CT in pediatric Hodgkin's lymphoma | |
dc.type | Makale | |
dc.relation.journal | TURK ONKOLOJI DERGISI-TURKISH JOURNAL OF ONCOLOGY | |
dc.contributor.department | Ankara Ataturk Training & Research Hospital , , | |
dc.identifier.volume | 30 | |
dc.identifier.issue | 4 | |
dc.identifier.startpage | 240 | |
dc.identifier.endpage | 251 | |
dc.contributor.firstauthorID | 219749 | |