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dc.contributor.authorNakatani, Koyaen
dc.contributor.authorNakamoto, Yujien
dc.contributor.authorWatanabe, Kenichiroen
dc.contributor.authorSaga, Tsuneoen
dc.contributor.authorHigashi, Tatsuyaen
dc.contributor.authorTogashi, Kaorien
dc.contributor.alternative中谷, 航也ja
dc.contributor.alternative中本, 裕士ja
dc.date.accessioned2013-08-06T01:05:46Z-
dc.date.available2013-08-06T01:05:46Z-
dc.date.issued2012-07-
dc.identifier.issn0363-9762-
dc.identifier.urihttp://hdl.handle.net/2433/177069-
dc.description.abstract[Purpose]: The usefulness of 18F fluorodeoxyglucose (FDG) positron emission tomography (PET) in pediatric Hodgkin lymphoma (p-HL) has been well demonstrated; however, pediatric non-Hodgkin lymphoma (p-NHL) has distinct characteristics from p-HL and adult NHL. We assessed roles of FDG PET in p-NHL. [Materials and Methods]: Nineteen patients with p-NHL underwent 80 scans. Scans for staging (group A, n = 6) and response assessment (group B, n = 42) were compared with conventional imaging modalities (CIMs). Scans within group B for end-chemotherapy assessment (subgroup B+, n = 11) and for post-therapeutic surveillance (group C, n = 32) were analyzed for diagnostic performance. [Results]: In group A, PET and CIM demonstrated comparable results. In group B, PET diagnoses were concordant with CIM in 21 and discordant in 11 studies. Of the discordant cases, PET suggested remnant lesions in 5 cases, whereas CIM suggested lesions in 6 cases. PET modified therapeutic strategy in 4 cases by detecting new extranodal lesions. In subgroup B+, sensitivity, specificity, and accuracy for predicting relapse were 50%, 71%, and 64%, respectively. In group C, sensitivity, specificity, and accuracy were 100%, 87%, and 88%, respectively, but positive predictive value was 33%. [Conclusions]: The role of FDG PET in p-NHL may be limited, unlike with p-HL or adult NHL. Nevertheless, FDG PET may serve complementarily in detecting unexpected lesions that can emerge in p-NHL.en
dc.format.mimetypeapplication/pdf-
dc.language.isoeng-
dc.publisherLippincott, Williams & Wilkinsen
dc.rights© 2012 Lippincott Williams & Wilkins.en
dc.rightsThis is not the published version. Please cite only the published version.en
dc.rightsこの論文は出版社版でありません。引用の際には出版社版をご確認ご利用ください。ja
dc.subject.meshAdolescenten
dc.subject.meshAdulten
dc.subject.meshChilden
dc.subject.meshChild, Preschoolen
dc.subject.meshFemaleen
dc.subject.meshFluorodeoxyglucose F18/diagnostic useen
dc.subject.meshHumansen
dc.subject.meshLymphoma, Non-Hodgkin/drug therapyen
dc.subject.meshLymphoma, Non-Hodgkin/radionuclide imagingen
dc.subject.meshMaleen
dc.subject.meshPositron-Emission Tomographyen
dc.subject.meshReference Standardsen
dc.subject.meshRemission Inductionen
dc.subject.meshWhole Body Imagingen
dc.subject.meshYoung Adulten
dc.titleRoles and limitations of FDG PET in pediatric non-Hodgkin lymphoma.en
dc.typejournal article-
dc.type.niitypeJournal Article-
dc.identifier.ncidAA0060791X-
dc.identifier.jtitleClinical nuclear medicineen
dc.identifier.volume37-
dc.identifier.issue7-
dc.identifier.spage656-
dc.identifier.epage662-
dc.relation.doi10.1097/RLU.0b013e318238f72b-
dc.textversionauthor-
dc.identifier.pmid22691506-
dc.relation.urlhttp://hdl.handle.net/2433/157424-
dcterms.accessRightsopen access-
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