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FDG-PET in T-cell and NK-cell neoplasms.

FDG-PET in T-cell and NK-cell neoplasms. Research Abstract Details 

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  • FDG-PET in T-cell and NK-cell neoplasms. Abstract Text:

    s kakoS Kako,k izutsuK Izutsu,y otaY Ota,y minataniY Minatani,m sugayaM Sugaya,t momoseT Momose,k ohtomoK Ohtomo,y kandaY Kanda,s chibaS Chiba,t motokuraT Motokura,m kurokawaM Kurokawa,s kakoS Kako,k izutsuK Izutsu,y otaY Ota,y minataniY Minatani,m sugayaM Sugaya,t momoseT Momose,k ohtomoK Ohtomo,y kandaY Kanda,s chibaS Chiba,t motokuraT Motokura,m kurokawaM Kurokawa,s kakoS Kako,k izutsuK Izutsu,y otaY Ota,y minataniY Minatani,m sugayaM Sugaya,t momoseT Momose,k ohtomoK Ohtomo,y kandaY Kanda,s chibaS Chiba,t motokuraT Motokura,m kurokawaM Kurokawa,

    BACKGROUND: A growing number of studies demonstrate the utility of (18)fluoro-2-deoxyglucose positron emission tomography (FDG-PET) in the management of malignant lymphoma. The results of FDG-PET, however, have not been studied extensively for T-cell and natural killer (NK)-cell neoplasms. PATIENTS AND METHODS: We retrospectively evaluated pretreatment FDG-PET scans in 41 patients with T/NK-cell neoplasms diagnosed according to the World Health Organization (WHO) classification. Histological subtypes frequently included were peripheral T-cell lymphoma, unspecified (PTCLu, n = 11), extranodal NK/T-cell lymphoma, nasal type (ENKL, n = 8), primary cutaneous anaplastic large cell lymphoma (C-ALCL, n = 5), and angioimmunoblastic T-cell lymphoma (AILT, n = 4). RESULTS: FDG-PET detected a lymphoma lesion in at least one site in 36 out of 41 patients. The positive rate was equally high in most histological subtypes except for cutaneous lymphomas: PTCLu 91%, ENKL 100%, C-ALCL 60%, AILT 100%. All the patients without an FDG-avid lesion had lesions restricted to skin. Among patients who had cutaneous lesions, only 50% had FDG-avid cutaneous lesions, all of which were tumorous. The positive rate of FDG-PET for bone marrow involvement was only 20%. CONCLUSION: T/NK-cell neoplasms incorporated in this study were generally FDG-avid except for cutaneous lesions and bone marrow involvement.

    FDG-PET in T-cell and NK-cell neoplasms. Publishing Authors By Initials

    s kakoS Kako,k izutsuK Izutsu,y otaY Ota,y minataniY Minatani,m sugayaM Sugaya,t momoseT Momose,k ohtomoK Ohtomo,y kandaY Kanda,s chibaS Chiba,t motokuraT Motokura,m kurokawaM Kurokawa,s kakoS Kako,k izutsuK Izutsu,y otaY Ota,y minataniY Minatani,m sugayaM Sugaya,t momoseT Momose,k ohtomoK Ohtomo,y kandaY Kanda,s chibaS Chiba,t motokuraT Motokura,m kurokawaM Kurokawa,s kakoS Kako,k izutsuK Izutsu,y otaY Ota,y minataniY Minatani,m sugayaM Sugaya,t momoseT Momose,k ohtomoK Ohtomo,y kandaY Kanda,s chibaS Chiba,t motokuraT Motokura,m kurokawaM Kurokawa,

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    FDG-PET in T-cell and NK-cell neoplasms. Journal Published:

    PUBLICATION TYPE: Journal Article

    Journal: Annals of oncology : official journal of the Europ

    VOLUME: 18

    Page Numbers: 1685-90

    Journal Abbreviation: Ann. Oncol.

    ISSN: 0923-7534

    DAY: 22

    MONTH: 08

    YEAR: 2007

    FDG-PET in T-cell and NK-cell neoplasms. Information

    Number of References:

    LANGUAGE: eng

    NlmUniqueID: 9007735

    FDG-PET in T-cell and NK-cell neoplasms. Keywords Mesh Terms:

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    Grant and Affiliation Information for FDG-PET in T-cell and NK-cell neoplasms.

    AFFILIATION: Department of Hematology & Oncology.

    Country: England

    England Research PublicationEngland Research Publication

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    MEDLINETA: Ann Oncol

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