Zusammenfassung
Für Staging und Restaging von primären und sekundären (malignen) Neoplasien des Skeletts
stellt die Skelettszintigraphie nach wie vor ein valides Verfahren dar. Sie findet
sich dabei aber in einer strengen Kosten/Nutzen-Diskussion und in Konkurrenz zu insbesondere
MRT und, z. B. beim Prostatakarzinom, zu Tumormarkern als Verlaufsparameter (z. B.
PSA). Obwohl für die Darstellung von Knochenmetastasen zahlenmäßig die Knochenmarkszintigraphie
sensitiver (läsionsbezogen) als die Skelettszintigraphie ist, hat sie sich routinemäßig
nicht durchgesetzt. Der klinische Stellenwert der F-18-Fluorid-PET ist noch nicht
vollständig geklärt. Die Positivdarstellung von Metastasen im Skelett ist mit weiteren
Radiopharmaka möglich, z. B. „unspezifisch” mit F-18-FDG oder „spezifisch (z. B. neuroendokrine
Tumoren) mit I-123-MIBG.
Abstract
Bone scintigraphy is still a valid procedure for staging and restaging of primary
and secondary malignancies of the skeleton. However, there is a strong discussion
about cost-effectiveness and, especially, with competing procedures like magnetic
resonance imaging, and, e. g. for prostate cancer, with tumor markers like PSA. Although
bone marrow scintigraphy is more sensitive for the detection of bone metastases (on
a lesion by lesion basis) than bone scintigraphy, it is routinely not the procedure
of choice. The clinical value of F-18-Fluoride PET is not fully clarified yet. The
direct imaging of bone metastases in positive contrast is possible with a number of
substances, nonspecific with F-18-FDG or more specific (e. g. neuroendocrine tumors)
with I-123-MIBG.
Schlüsselwörter
Knochentumor - Knochenneoplasie - Szintigraphie
Key words
Bone tumor - scintigraphy
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Priv.-Doz. Dr. Dirk Sandrock
Klinik und Poliklinik für Nuklearmedizin
Universitätsklinikum Charité
Medizinische Fakultät der Humboldt-Universität zu Berlin
Schumannstr. 20/21
10098 Berlin
Phone: +49/30/4 50 52 70 12
Fax: +49/30/4 50 52 79 12
Email: dirk.sandrock@charite.de