Show simple item record

Regional 2-[ 18 F]fluoro-2-deoxy- d -glucose uptake varies in normal lung

dc.contributor.authorMiyauchi, Tsutomuen_US
dc.contributor.authorWahl, Richard L.en_US
dc.date.accessioned2006-09-11T18:16:08Z
dc.date.available2006-09-11T18:16:08Z
dc.date.issued1996-05en_US
dc.identifier.citationMiyauchi, Tsutomu; Wahl, Richard L.; (1996). "Regional 2-[ 18 F]fluoro-2-deoxy- d -glucose uptake varies in normal lung." European Journal of Nuclear Medicine 23(5): 517-523. <http://hdl.handle.net/2027.42/46841>en_US
dc.identifier.issn1619-7089en_US
dc.identifier.issn0340-6997en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/46841
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=8698055&dopt=citationen_US
dc.description.abstract2-[ 18 F]fluoro-2-deoxy- d -glucose positron emission tomography (FDG-PET) is a promising imaging procedure for detecting primary and metastatic cancer in the lungs. We have, however, failed to detect some small tumors in the lower lobes of the lungs. This study aimed to determine whether increase 18 F background activity in the dependent lower lungs is present, which could make lesion detection more difficult. We measured the standardized uptake values (SUVs) for FDG of normal lung remote from the nodular lesion in 16 patients with newly diagnosed untreated lung lesions stronlgy suspected to represent non-small cell lung cancers. In addition, 15 patients with known or suspected primary breast cancers without pulmonary lesions were included as control subjects. After PET transmission images of the thorax were obtained, approximately 370 MBq of FDG was injected intravenously and imaging was immediately begun. Patients were supine throughout the study. SUVs were determined with images obtained 50–70 min after FDG injection. Regions of interest (ROls) of 6×6 pixels were positioned over normal lung in anterior, mid, and posterior portions of upper, middle, and lower lung fields. Thus, as many as 18 ROls were positioned in each patient. The SUVs of the posterior portion were significantly higher than those of the anterior and mid portions in the population of 31 cases ( P <0.001). Also, the mean SUV of the lower lung field was significantly higher than the SUVs of the upper and middle lung fields in this population ( P <0.01). This pattern was seen among the two groups of 16 patients suspected of having lung cancer and 15 control subjects. Background 18 F activity was highest in posterior and lower lung in these patients. The maximum value of mean SUV observed in normal posterior lower lung was 0.804±0.230 (41% greater than the mean SUV in the anterior upper lung), which is in the range of the apparent SUV for a 5-mm lung lesion, with higher SUV, due to recovery coefficient issues. Thus this phenomenon could contribute to occasional false-negative lesions in those areas. Increased blood flow and FDG delivery and also scatter from heart and liver may contribute to the increased lower lung background activity. Regional differences in normal lung FDG uptake are significant and should be considered when interpreting pulmonary PET studies in patients with suspected primary or metastatic lung cancer.en_US
dc.format.extent661598 bytes
dc.format.extent3115 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherSpringer-Verlagen_US
dc.subject.other2[ 18 F]Fluoro-2-Deoxy- D -Glucoseen_US
dc.subject.otherPositron Emission Tomographyen_US
dc.subject.otherStandardized Uptake Valueen_US
dc.subject.otherMedicine & Public Healthen_US
dc.subject.otherImaging / Radiologyen_US
dc.subject.otherNuclear Medicineen_US
dc.subject.otherLungen_US
dc.titleRegional 2-[ 18 F]fluoro-2-deoxy- d -glucose uptake varies in normal lungen_US
dc.typeArticleen_US
dc.subject.hlbsecondlevelRadiologyen_US
dc.subject.hlbsecondlevelPhysicsen_US
dc.subject.hlbsecondlevelBiological Chemistryen_US
dc.subject.hlbtoplevelScienceen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDivision of Nuclear Medicine, Department of Internal Medicine, University of Michigan, Ann Arbor, Michigan, USAen_US
dc.contributor.affiliationumDivision of Nuclear Medicine, Department of Internal Medicine, University of Michigan, Ann Arbor, Michigan, USA; Division of Nuclear Medicine, University of Michigan Medical Center, 1500 E Medical Center Dr., B1G 412, 48109-0028, Ann Arbor, MI, USAen_US
dc.contributor.affiliationumcampusAnn Arboren_US
dc.identifier.pmid8698055en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/46841/1/259_2004_Article_BF00833385.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1007/BF00833385en_US
dc.identifier.sourceEuropean Journal of Nuclear Medicineen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


Files in this item

Show simple item record

Remediation of Harmful Language

The University of Michigan Library aims to describe library materials in a way that respects the people and communities who create, use, and are represented in our collections. Report harmful or offensive language in catalog records, finding aids, or elsewhere in our collections anonymously through our metadata feedback form. More information at Remediation of Harmful Language.

Accessibility

If you are unable to use this file in its current format, please select the Contact Us link and we can modify it to make it more accessible to you.