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Metabolic Characteristics of Castleman Disease on F-18-FDG PET in Relation to Clinical Implication

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dc.contributor.authorLee, Eun Seong-
dc.contributor.authorPaeng, Jin Chul-
dc.contributor.authorPark, Chang Min-
dc.contributor.authorChang, Won-
dc.contributor.authorLee, Won Woo-
dc.contributor.authorKang, Keon Wook-
dc.contributor.authorChung, June-Key-
dc.contributor.authorLee, Dong Soo-
dc.date.accessioned2024-08-08T01:43:57Z-
dc.date.available2024-08-08T01:43:57Z-
dc.date.created2021-01-22-
dc.date.created2021-01-22-
dc.date.issued2013-05-
dc.identifier.citationClinical Nuclear Medicine, Vol.38 No.5, pp.339-342-
dc.identifier.issn0363-9762-
dc.identifier.urihttps://hdl.handle.net/10371/207653-
dc.description.abstractPurpose: Castleman disease (CD) is a benign lymphoproliferative disease, which usually shows hypermetabolism on F-18-FDG PET/CT. In this study, we investigated metabolic characteristics of CD in consecutive series of patients and analyzed F-18-FDG uptake with regard to major clinicopathologic factors, to investigate clinical implication of F-18-FDG uptake in CD. Methods: Twelve patients (5 men and 7 women; mean age, 52 T 14 years) with pathologically confirmed CD, who underwent F-18-FDG PET/CT, were retrospectively enrolled, and their images were analyzed. The cases were composed of 10 first diagnosed and 2 relapsed cases. SUVmax was measured for each lesion. Metabolic characteristics were compared according to clinical and pathologic characteristics. Results: All the F-18-FDG PET/CT images showed hypermetabolic lesions including small lymph nodes of less than 1 cm. The average SUVmax was 5.8 T 4.1 with a varying range of 2.4 to 17.1. SUVmax was significantly higher in multicentric than in unicentric disease cases (7.0 +/- 4.6 vs 3.3 +/- 1.1; P = 0.048) and in the patients with clinical manifestation than the other group (7.1 +/- 4.5 and 3.1 +/- 0.8, respectively; P = 0.028). Conclusions: F-18-FDG PET/CT is an effective diagnostic imaging for diagnosis of CD. Castleman disease shows moderately increased F-18-FDG uptake. In addition, the uptake is well correlated with disease multicentricity and clinical manifestation, suggesting that it would be a significant imaging marker for severity or prognosis of CD.-
dc.language영어-
dc.publisherLippincott Williams & Wilkins Ltd.-
dc.titleMetabolic Characteristics of Castleman Disease on F-18-FDG PET in Relation to Clinical Implication-
dc.typeArticle-
dc.identifier.doi10.1097/RLU.0b013e3182816730-
dc.citation.journaltitleClinical Nuclear Medicine-
dc.identifier.wosid000317400400014-
dc.identifier.scopusid2-s2.0-84876414513-
dc.citation.endpage342-
dc.citation.number5-
dc.citation.startpage339-
dc.citation.volume38-
dc.description.isOpenAccessN-
dc.contributor.affiliatedAuthorPark, Chang Min-
dc.contributor.affiliatedAuthorLee, Won Woo-
dc.contributor.affiliatedAuthorKang, Keon Wook-
dc.contributor.affiliatedAuthorChung, June-Key-
dc.contributor.affiliatedAuthorLee, Dong Soo-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.subject.keywordPlusANTIBODY-
dc.subject.keywordPlusRECEPTOR-
dc.subject.keywordPlusPATIENT-
dc.subject.keywordAuthorCastleman disease-
dc.subject.keywordAuthorF-18-FDG PET/CT-
dc.subject.keywordAuthorunicentric-
dc.subject.keywordAuthormulticentric-
dc.subject.keywordAuthorSUVmax-
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  • Department of Medicine
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