Ji-Hyoung Seo
Kyungpook National University Hospital
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Journal of Psychiatric Research | 2009
Yang-Tae Kim; Sang-Woo Lee; Do-Hoon Kwon; Ji-Hyoung Seo; Byeong-Cheol Ahn; Jaetae Lee
OBJECTIVE Although a lot of evidence from neuropsychological and neuroimaging studies supports the view that patients with substance dependence have abnormalities in the prefrontal cortex, functional deficits in the prefrontal cortex have not been fully investigated in methamphetamine (MA) dependent patients. This study was prepared to examine whether MA abusers have cerebral metabolic abnormalities and executive dysfunction. METHOD Twenty-four abstinent MA dependent patients and 21 age-matched control subjects underwent resting brain FDG-PET and completed computerized versions of the Wisconsin card sorting test (WCST). Resting brain PET images were obtained 30min after an intravenous injection of 370MBq of (18)F-FDG. Significant differences in glucose metabolism were estimated for every voxel using t-statistics on SPM2 implemented in Matlab. RESULTS Resting brain FDG-PET revealed significant hypometabolism in the left inferior frontal white matter (Talairach coordinates (x, y, z): -34, 7, 31) in MA dependent patients compared to the control subjects (corrected p=0.001, peak Z=5.37, voxel number 201). The nearest gray matter region was the left inferior frontal cortex (Brodmann area 9). There were negative correlations between the relative regional cerebral metabolism for glucose (rCMRglc) in the left inferior frontal white matter and the total cumulative dose of MA (r=-0.57, p<0.01). MA dependent patients completed significantly fewer categories (3.8+/-2.2) and made more perseveration errors (21.3+/-11.8) and total errors (43.5+/-19.5) on the WCST when compared to the control subjects (p<0.01). CONCLUSIONS These data suggest that MA dependent patients have dose-dependent frontal hypometabolism and frontal executive dysfunction.
European Journal of Nuclear Medicine and Molecular Imaging | 2010
Shin Young Jeong; Sang-Woo Lee; Hui Joong Lee; Sungmin Kang; Ji-Hyoung Seo; Kyung Ah Chun; Ihn Ho Cho; Kyung Sook Won; Seok Kil Zeon; Byeong-Cheol Ahn; Jaetae Lee
PurposeThe purpose of this study was to determine the incidence of incidental pituitary uptake on whole-body 18F-fluorodeoxyglucose (FDG) positron emission tomography/computed tomography (PET/CT) and to investigate its clinical significance.MethodsThe files of 40,967 patients who underwent whole-body FDG PET/CT were retrospectively reviewed. Quantification of pituitary metabolic activity was obtained by using the maximum standardized uptake value (SUVmax). Hormone assays and pituitary MRIs were performed to assess pituitary lesions.ResultsFocally increased pituitary FDG uptake on PET/CT was found in 30 of 40,967 patients, accounting for an incidence of 0.073%. The mean SUVmax of 30 patients was 8.9 ± 6.6 (range: 3.2–32.6). Histological diagnosis was obtained in three patients and included two growth hormone-secreting adenomas and one non-functioning adenoma. Hormone assays were performed on serum samples from 11 patients, 2 of whom were shown to have hypersecretion of pituitary hormone. MRI was performed on 19 patients. Abnormal MRI findings suggesting a pituitary mass were found in 18 of 19 cases (94.7%). The mean SUVmax calculated without correction for partial volume effect for macroadenomas was significantly higher than the SUVmax for microadenomas (11.5 ± 8.4 vs 4.8 ± 1.3; p < 0.05). There were no cases diagnosed with metastasis to the pituitary gland during clinical follow-up.ConclusionIncidental pituitary FDG uptake was a very rare finding. Cases with incidental pituitary FDG uptake were diagnosed primarily with clinically non-functioning adenomas, and there were also a few functioning adenomas. Further evaluations, including hormone assays and pituitary MRI, are warranted when pituitary uptake is found on FDG PET/CT.
Clinical Nuclear Medicine | 2012
Jong-Ryool Oh; Jung-Joon Min; Ho-Chun Song; Ari Chong; Ga-Eon Kim; Chan Choi; Ji-Hyoung Seo; Hee-Seung Bom
PURPOSE The purpose of this study was to suggest a new diagnostic strategy using metabolic volume (MV) and maximum standardized uptake value (SUVmax) to differentiate malignancy and dysplasia from benign colonic 2-deoxy-2-18F-fluoro-D-glucose (FDG) uptakes. MATERIALS AND METHODS From records of 21,317 consecutive FDG positron emission tomography/computed tomography (PET/CT) scans at 2 centers, 102 focal colonic lesions in 99 patients investigated by colonoscopy and histopathologic examination were eligible for this retrospective study. SUVmax and MV were compared according to colonoscopic and histopathologic results. Firstly, dysplasia was separated from malignancy and benign lesions. Secondly, malignancy and benign lesions were separated from each other. The better parameters of each step were determined, and a diagnostic strategy was developed from their combination. RESULTS A total of 102 incidental colonic FDG uptakes were revealed as 32 malignancies, 43 dysplasias, and 27 benign lesions. MV better differentiated dysplasia from malignancy and benign lesions (cutoff value, ≤3.14 cm3; area under the receiver-operating characteristic curve [AUC] = 0.947), and SUVmax better differentiated malignancy from benign lesions (cutoff value, >9.1; AUC = 0.934). Overall, the stepwise algorithm using MV and SUVmax (AUC = 0.886) was superior to single measurements of SUVmax (AUC = 0.750) and MV (AUC = 0.714) for differentiating malignancy and dysplasia from benign lesions; sensitivity: 92%, specificity: 85%, accuracy: 90%, positive predictive value: 94%, negative predictive value: 79%. CONCLUSIONS The stepwise approach using MV and SUVmax was able to differentiate malignancy and dysplasia from benign colonic FDG uptakes on PET/CT. Colonic FDG uptake with MV ≤3.14 cm3 had a high probability of dysplasia. MV >3.14 cm3 and SUVmax >9.1 indicated malignancy, whereas MV >3.14 cm3 and SUVmax ≤9.1 indicated benign lesions.
Lung Cancer | 2013
Jong-Ryool Oh; Ji-Hyoung Seo; Chae Moon Hong; Shin Young Jeong; Sang-Woo Lee; Jaetae Lee; Jung-Joon Min; Ho-Chun Song; Hee-Seung Bom; Young-Chul Kim; Byeong-Cheol Ahn
PURPOSE The aim of this study was to evaluate the relationship and difference in prognostic significance between whole-body tumor burden, thoracic tumor burden, and extra-thoracic tumor burden on (18)F-FDG PET/CT for patients with extensive-disease small cell lung cancer (ED-SCLC). MATERIALS AND METHODS We performed a retrospective, two-center analysis for patients with ED-SCLC who underwent pretreatment (18)F-FDG PET/CT. Metabolic tumor burden was estimated using whole-body metabolic tumor volume (MTV(WB)), thoracic metabolic tumor volume (MTV(TRX)), extra-thoracic metabolic tumor volume (MTV(EXT)), and the number of extra-thoracic tumor foci. Uni- and multivariate analyses were performed using various clinical factors and the metabolic indices. RESULTS A total of 91 patients were eligible for this study. MTV(WB) showed stronger correlation with MTV(EXT) than MTV(TRX) (r(2) = 0.804 vs. 0.132, p < 0.001, both), whereas no correlation was observed between MTV(EXT) and MTV(TRX) (r(2) = 0.007, p = 0.428). Patients with smaller MTV(WB), MTV(EXT), and extra-thoracic tumor foci showed longer survival than patients with larger MTV(WB), MTV(EXT), and extra-thoracic tumor foci, respectively, whereas the survival difference between patients with smaller MTV(TRX) and those with larger MTV(TRX) was not significant. Results of uni- and multivariate analyses showed that ECOG performance status (HR = 2.31, p = 0.015), initial chemotherapy cycles (HR = 0.24, p < 0.001), and the number of extra-thoracic tumor foci (HR = 2.75, p < 0.001) were independent prognostic factors for overall survival, and initial chemotherapy cycles (HR = 0.25, p < 0.001), and MTV(EXT) (HR = 2.04, p = 0.013) were independent prognostic factors for progression-free survival. CONCLUSION These data provide evidence indicating that extra-thoracic tumor burden but not thoracic tumor burden is an independent prognostic biomarker for ED-SCLC, and support further exploration of novel treatment strategies targeting extra-thoracic tumor burden in order to improve the clinical outcomes of patients with ED-SCLC.
Clinical Nuclear Medicine | 2010
Sungmin Kang; Bong-Il Song; Hong Je Lee; Shin Young Jeong; Ji-Hyoung Seo; Sang-Woo Lee; Byeong-Cheol Ahn; Jaetae Lee; Hui-Joong Lee
Abstract: Facial muscle is a very rare site for distant metastasis of renal cell carcinoma (RCC). We present a 71-year-old man with isolated facial muscle metastasis 12 years after right nephrectomy for RCC. Magnetic resonance imaging showed a soft-tissue mass in the masticator space. F-18 fluorodeoxyglucose positron emission tomography/computed tomography showed a large hypermetabolic lesion in the right masticator space without other hypermetabolic lesion in the whole body. Subsequent biopsy and histologic study confirmed metastatic cancer from RCC.
Clinical Nuclear Medicine | 2010
Bong-Il Song; Sang-Woo Lee; Hong Je Lee; Sungmin Kang; Shin Young Jeong; Ji-Hyoung Seo; Byeong-Cheol Ahn; Jaetae Lee; Kyung-Min Shin
Abstract:Pulmonary drug toxicity is increasingly being diagnosed as a cause of acute and chronic lung disease. We report a case of drug-induced pneumonitis after R-CHOP therapy for non-Hodgkin lymphoma in which a follow-up examination F-18 FDG PET/CT showed some patchy consolidations and ground-glas
European Journal of Nuclear Medicine and Molecular Imaging | 2012
Jong-Ryool Oh; Ji-Hyoung Seo; Ari Chong; Jung-Joon Min; Ho-Chun Song; Young-Chul Kim; Hee-Seung Bom
Thyroid | 2007
Sang-Woo Lee; Jaetae Lee; Hui Joong Lee; Ji-Hyoung Seo; Seong-Min Kang; Jin-Ho Bae; Byeong-Cheol Ahn
Nuclear Medicine Communications | 2009
Sang-Woo Lee; Jaetae Lee; Jin-Ho Bae; Ji-Hyoung Seo; Seong-Min Kang; Byeong-Cheol Ahn; In-Kyu Lee
Nuclear Medicine and Molecular Imaging | 2009
Hong-Je Lee; Bong-Il Song; Sungmin Kang; Shin Young Jeong; Ji-Hyoung Seo; Sang-Woo Lee; Jeongsoo Yoo; Byeong-Cheol Ahn; Jaetae Lee