Cited 11 times in
The performance of contrast-enhanced FDG PET/CT for the differential diagnosis of unexpected ovarian mass lesions in patients with nongynecologic cancer
DC Field | Value | Language |
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dc.contributor.author | 조응혁 | - |
dc.contributor.author | 강원준 | - |
dc.contributor.author | 김영태 | - |
dc.contributor.author | 윤미진 | - |
dc.contributor.author | 이재훈 | - |
dc.contributor.author | 이정원 | - |
dc.contributor.author | 이종두 | - |
dc.date.accessioned | 2016-02-04T10:58:28Z | - |
dc.date.available | 2016-02-04T10:58:28Z | - |
dc.date.issued | 2015 | - |
dc.identifier.issn | 0363-9762 | - |
dc.identifier.uri | https://ir.ymlib.yonsei.ac.kr/handle/22282913/139388 | - |
dc.description.abstract | PURPOSE: This study aimed to evaluate the diagnostic accuracy of contrast-enhanced FDG PET/CT for unexpected ovarian lesions in patients with nongynecologic cancers. PATIENTS AND METHODS: The present retrospective study was approved by the hospital institutional review board. We enrolled 72 nongynecologic cancer patients (33 colorectal cancer, 20 breast cancer, and 19 gastric cancer) who showed unexpected ovarian lesions on contrast-enhanced FDG PET/CT and subsequently underwent surgical resection of the ovarian lesions. The SUVmax values of the ovarian lesions were compared according to the histopathological results, and the accuracy of PET/CT was evaluated. RESULTS: A total of 103 ovarian lesions were surgically resected from 72 patients (64 ovarian lesions were metastases, 21 were benign, and 18 were malignant primary ovarian cancer). SUVmax among the 3 groups were different (P < 0.0001). Using a cutoff SUVmax of 2.5, the sensitivity, specificity, and accuracy of PET/CT for detecting malignant ovarian lesions were 80.5%, 81.0%, and 80.6%, respectively. Detection rates of PET/CT for colorectal, breast, and gastric cancer metastases, as well as primary ovarian cancers were 91.4%, 83.3%, 47.8%, and 100.0%, respectively. Using contrast-enhanced CT findings with SUVmax, the sensitivity, specificity, and accuracy of contrast-enhanced FDG PET/CT were improved to 95.1%, 76.2%, and 91.3%, respectively (P = 0.003). CONCLUSIONS: Conventional FDG PET/CT showed moderate diagnostic accuracy for the detection of malignant ovarian lesions mainly due to low detection rate in gastric cancer metastases. The PET/CT detection rate of malignant ovarian lesions can be improved using contrast-enhanced CT findings with FDG uptake measurement. | - |
dc.description.statementOfResponsibility | open | - |
dc.format.extent | 97~102 | - |
dc.relation.isPartOf | CLINICAL NUCLEAR MEDICINE | - |
dc.rights | CC BY-NC-ND 2.0 KR | - |
dc.rights.uri | https://creativecommons.org/licenses/by-nc-nd/2.0/kr/ | - |
dc.subject.MESH | Adult | - |
dc.subject.MESH | Aged | - |
dc.subject.MESH | Aged, 80 and over | - |
dc.subject.MESH | Breast Neoplasms/diagnostic imaging | - |
dc.subject.MESH | Breast Neoplasms/pathology* | - |
dc.subject.MESH | Case-Control Studies | - |
dc.subject.MESH | Colorectal Neoplasms/diagnostic imaging | - |
dc.subject.MESH | Colorectal Neoplasms/pathology* | - |
dc.subject.MESH | Contrast Media | - |
dc.subject.MESH | Diagnosis, Differential | - |
dc.subject.MESH | Female | - |
dc.subject.MESH | Fluorodeoxyglucose F18* | - |
dc.subject.MESH | Humans | - |
dc.subject.MESH | Middle Aged | - |
dc.subject.MESH | Multimodal Imaging | - |
dc.subject.MESH | Ovarian Neoplasms/diagnostic imaging* | - |
dc.subject.MESH | Ovarian Neoplasms/secondary | - |
dc.subject.MESH | Positron-Emission Tomography* | - |
dc.subject.MESH | Radiopharmaceuticals* | - |
dc.subject.MESH | Retrospective Studies | - |
dc.subject.MESH | Sensitivity and Specificity | - |
dc.subject.MESH | Tomography, X-Ray Computed* | - |
dc.title | The performance of contrast-enhanced FDG PET/CT for the differential diagnosis of unexpected ovarian mass lesions in patients with nongynecologic cancer | - |
dc.type | Article | - |
dc.contributor.college | College of Medicine (의과대학) | - |
dc.contributor.department | Dept. of Obstetrics & Gynecology (산부인과학) | - |
dc.contributor.googleauthor | Lee, Jeong Won | - |
dc.contributor.googleauthor | Lee, Jae-Hoon | - |
dc.contributor.googleauthor | Cho, Arthur | - |
dc.contributor.googleauthor | Yun, Mijin | - |
dc.contributor.googleauthor | Lee, Jong Doo | - |
dc.contributor.googleauthor | Kim, Young Tae | - |
dc.contributor.googleauthor | Kang, Won Jun | - |
dc.identifier.doi | 10.1097/RLU.0000000000000667 | - |
dc.admin.author | false | - |
dc.admin.mapping | false | - |
dc.contributor.localId | A03887 | - |
dc.contributor.localId | A00062 | - |
dc.contributor.localId | A00729 | - |
dc.contributor.localId | A02550 | - |
dc.contributor.localId | A03117 | - |
dc.contributor.localId | A03138 | - |
dc.contributor.localId | A03093 | - |
dc.relation.journalcode | J00595 | - |
dc.identifier.eissn | 1536-0229 | - |
dc.identifier.pmid | 25546187 | - |
dc.identifier.url | http://ovidsp.ovid.com/ovidweb.cgi?T=JS&CSC=Y&NEWS=N&PAGE=fulltext&AN=00003072-201502000-00001&LSLINK=80&D=ovft | - |
dc.subject.keyword | Krukenberg tumor | - |
dc.subject.keyword | ¹⁸F-FDG | - |
dc.subject.keyword | PET | - |
dc.subject.keyword | ovary | - |
dc.subject.keyword | metastasis | - |
dc.contributor.alternativeName | Cho, Arthur Eung Hyuck | - |
dc.contributor.alternativeName | Kang, Won Jun | - |
dc.contributor.alternativeName | Kim, Young Tae | - |
dc.contributor.alternativeName | Yun, Mi Jin | - |
dc.contributor.alternativeName | Lee, Jae Hoon | - |
dc.contributor.alternativeName | Lee, Jeong Won | - |
dc.contributor.alternativeName | Lee, Jong Doo | - |
dc.contributor.affiliatedAuthor | Cho, Arthur Eung Hyuck | - |
dc.contributor.affiliatedAuthor | Kang, Won Jun | - |
dc.contributor.affiliatedAuthor | Kim, Young Tae | - |
dc.contributor.affiliatedAuthor | Yun, Mi Jin | - |
dc.contributor.affiliatedAuthor | Lee, Jeong Won | - |
dc.contributor.affiliatedAuthor | Lee, Jong Doo | - |
dc.contributor.affiliatedAuthor | Lee, Jae Hoon | - |
dc.rights.accessRights | not free | - |
dc.citation.volume | 40 | - |
dc.citation.number | 2 | - |
dc.citation.startPage | 97 | - |
dc.citation.endPage | 102 | - |
dc.identifier.bibliographicCitation | CLINICAL NUCLEAR MEDICINE, Vol.40(2) : 97-102, 2015 | - |
dc.identifier.rimsid | 54917 | - |
dc.type.rims | ART | - |
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