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Featured researches published by Tomohiro Yoneyama.


Clinical Nuclear Medicine | 2011

F-18 FDG uptake patterns and disease activity of collagen vascular diseases-associated arthritis.

Tetsuhiko Okabe; Hirofumi Shibata; Kazuya Shizukuishi; Tomohiro Yoneyama; Tomio Inoue; Ukihide Tateishi

Purpose: The purpose of the present study was to investigate F-18 FDG uptake patterns, and to see whether joint F-18 FDG uptake reflected disease activity in patients with collagen vascular diseases (CVD)-associated arthritis. Materials and Methods: A total of 72 patients with CVD-associated arthritis and 30 control subjects who underwent F-18 FDG PET or PET/CT were retrospectively investigated. PET images of 12 major joints, 7 minor joints, and extra-articular accumulation were assessed. We investigated F-18 FDG uptake patterns and the relationships between the degree of F-18 FDG uptake and distribution, clinical symptoms, and laboratory test results. Results: Remitting seronegative symmetric synovitis with pitting edema syndrome, mixed connective tissue disease, rheumatoid arthritis, and systemic sclerosis tended to show strong and multiple joint F-18 FDG uptake. F-18 FDG uptake was found in bone marrow (86%) and/or spleen (57%) in 7 patients with adult-onset Still disease. The maximum standardized uptake value (SUVmax) correlated with the counts of erythrocyte sedimentation rate, matrix metalloproteinase-3, IgG, and IgA. Joint swelling had a positive association with SUVmax. Multiple logistic regression analyses revealed that factor associated with increased SUVmax of the joint was joint swelling (P = 0.005). Conclusions: The degree of joint F-18 FDG uptake may contribute to predict active inflammatory process of the joint. In addition, F-18 FDG uptake patterns may have a potential which helps differential diagnosis of CVD-associated arthritis.


European Journal of Nuclear Medicine and Molecular Imaging | 2014

Tumor hypoxia and microscopic diffusion capacity in brain tumors: A comparison of 62 Cu-Diacetyl-Bis (N4-Methylthiosemicarbazone) PET/CT and diffusion-weighted MR imaging

Ayako Hino-Shishikura; Ukihide Tateishi; Hirofumi Shibata; Tomohiro Yoneyama; Toshiaki Nishii; Ikuo Torii; Kensuke Tateishi; Makoto Ohtake; Nobutaka Kawahara; Tomio Inoue

ObjectivesThe aim of this study was to clarify the relationship between tumor hypoxia and microscopic diffusion capacity in primary brain tumors using 62Cu-Diacetyl-Bis (N4-Methylthiosemicarbazone) (62Cu-ATSM) PET/CT and diffusion-weighted MR imaging (DWI).MethodsThis study was approved by the institutional human research committee and was HIPAA compliant, and informed consent was obtained from all patients. 62Cu-ATSM PET/CT and DWI were performed in a total of 40 primary brain tumors of 34 patients with low grade glioma (LGG, n = 13), glioblastoma (GBM, n = 20), and primary central nervous system lymphoma (PCNSL, n = 7). 62Cu-ATSM PET/CT parameters and apparent diffusion coefficient (ADC) obtained by DWI were compared.ResultsHigh intensity signals by 62Cu-ATSM PET/CT and DWI in patients with GBM and PCNSL, and low intensity signals in LGG patients were observed. An inverse correlation was found between maximum SUV (SUVmax) and minimum ADC (ADCmin) (r = −0.583, p < 0.0001), and between tumor/brain ratio (T/Bratio) and ADCmin for all tumors (r = −0.532, p < 0.0001). Both SUVmax and T/Bratio in GBM were higher than LGG (p < 0.0001 and p < 0.0001), and those in PCNSL were also higher than GBM (p = 0.033 and p = 0.044). The ADCmin was lower in GBM (p = 0.011) and PCNSL (p = 0.01) than in LGG, while no significant difference was found between GBM and PCNSL (p = 0.90).ConclusionTumor hypoxia assessed by 62Cu-ATSM PET/CT correlated with microscopic diffusion capacity obtained by DWI in brain tumors. Both 62Cu-ATSM PET/CT and DWI were considered feasible imaging methods for grading glioma. However, 62Cu-ATSM PET/CT provided additional diagnostic information to differentiate between GBM and PCNSL.


European Journal of Radiology | 2014

Staging accuracy of pancreatic cancer: Comparison between non-contrast-enhanced and contrast-enhanced PET/CT

Tomohiro Yoneyama; Ukihide Tateishi; Itaru Endo; Tomio Inoue

PURPOSE Our aim was to clarify the diagnostic impact of contrast-enhanced (CE) (18)F-fluorodeoxyglucose (FDG)-positron emission tomography (PET)/computed tomography (CT) for staging of pancreatic cancer compared to non-CE PET/CT. METHOD AND MATERIALS Between April 2006 and November 2009, a total of 95 patients (age range, 36-83 years [mean age, 67]) with primary pancreatic cancer underwent (18)F-FDG PET/CT examinations. Diagnostic accuracy was compared between non-CE PET/CT and CE PET/CT. Images were analyzed visually and quantitatively by two blinded reviewers. Reference standard was histological examination in 48 patients (51%) and/or confirmation of an obvious progression in number and/or size of the lesions on follow-up CT examinations in 47 patients (49%). RESULTS For T-staging, invasion of duodenum (n=20, 21%), mesentery (n=12, 13%), and retroperitoneum (n=13, 14%) was correctly diagnosed by both modalities. The ROC analyses revealed that the Az values of celiac artery (CA), common hepatic artery (CHA), splenic artery (SV), and superior mesenteric vein (SMV) invasion were significantly higher in the CE PET/CT group for both readers. Nodal metastasis was correctly diagnosed by CE PET/CT in 38 patients (88%) and by non-CE PET/CT in 45 patients (87%). Diagnostic accuracies of nodal metastasis in two modalities were similar. Using CE PET/CT, distant metastasis, scalene node metastasis, and peritoneal dissemination were correctly assigned in 39 patients (91%), while interpretation based on non-CE PET/CT revealed distant metastasis, scalene node metastasis, and peritoneal dissemination in 42 patients (81%). Diagnostic accuracy of distant metastasis, scalene node metastasis, and peritoneal dissemination with CE PET/CT was significantly higher than that of non-CE PET/CT (p<0.05). CONCLUSION CE PET/CT allows a more precise assessment of distant metastasis, scalene node metastasis, and peritoneal dissemination in patients with pancreatic cancer.


British Journal of Neurosurgery | 2018

Three-dimensional multimodality fusion imaging as an educational and planning tool for deep-seated meningiomas

Mitsuru Sato; Kensuke Tateishi; Hidetoshi Murata; Taichi Kin; Jun Suenaga; Hajime Takase; Tomohiro Yoneyama; Toshiaki Nishii; Ukihide Tateishi; Tetsuya Yamamoto; Nobuhito Saito; Tomio Inoue; Nobutaka Kawahara

Abstract Introduction: The utility of surgical simulation with three-dimensional multimodality fusion imaging (3D-MFI) has been demonstrated. However, its potential in deep-seated brain lesions remains unknown. The aim of this study was to investigate the impact of 3D-MFI in deep-seated meningioma operations. Material and Methods: Fourteen patients with deeply located meningiomas were included in this study. We constructed 3D-MFIs by fusing high-resolution magnetic resonance (MR) and computed tomography (CT) images with a rotational digital subtraction angiogram (DSA) in all patients. The surgical procedure was simulated by 3D-MFI prior to operation. To assess the impact on neurosurgical education, the objective values of surgical simulation by 3D-MFIs/virtual reality (VR) video were evaluated. To validate the quality of 3D-MFIs, intraoperative findings were compared. The identification rate (IR) and positive predictive value (PPV) for the tumor feeding arteries and involved perforating arteries and veins were also assessed for quality assessment of 3D-MFI. Results: After surgical simulation by 3D-MFIs, near-total resection was achieved in 13 of 14 (92.9%) patients without neurological complications. 3D-MFIs significantly contributed to the understanding of surgical anatomy and optimal surgical view (p < .0001) and learning how to preserve critical vessels (p < .0001) and resect tumors safety and extensively (p < .0001) by neurosurgical residents/fellows. The IR of 3D-MFI for tumor-feeding arteries and perforating arteries and veins was 100% and 92.9%, respectively. The PPV of 3D-MFI for tumor-feeding arteries and perforating arteries and veins was 98.8% and 76.5%, respectively. Conclusions: 3D-MFI contributed to learn skull base meningioma surgery. Also, 3D-MFI provided high quality to identify critical anatomical structures within or adjacent to deep-seated meningiomas. Thus, 3D-MFI is promising educational and surgical planning tool for meningiomas in deep-seated regions.


Annals of Nuclear Medicine | 2013

Role of 18F-fluoride PET/CT in the assessment of multiple myeloma: initial experience

Yuji Nishiyama; Ukihide Tateishi; Kazuya Shizukuishi; Ayako Shishikura; Etsuko Yamazaki; Hiroto Shibata; Tomohiro Yoneyama; Yoshiaki Ishigatsubo; Tomio Inoue


Japanese Journal of Radiology | 2014

Correlation of metabolic tumor volume and 11C-choline uptake with the pathology of prostate cancer: evaluation by use of simultaneously recorded MR and PET images

Tomohiro Yoneyama; Ukihide Tateishi; Takashi Terauchi; Tomio Inoue


Skeletal Radiology | 2012

Age-related changes in pre- and postmenopausal women investigated with 18F-fluoride PET—a preliminary study

Seiji Kurata; Kazuya Shizukuishi; Ukihide Tateishi; Tomohiro Yoneyama; Ayako Hino; Masatoshi Ishibashi; Tomio Inoue


Annals of Nuclear Medicine | 2013

Assessment of atherosclerosis in oncologic patients using 18F-fluoride PET/CT

Seiji Kurata; Ukihide Tateishi; Kazuya Shizukuishi; Tomohiro Yoneyama; Ayako Hino; Hayato Kaida; Kiminori Fujimoto; Masatoshi Ishibashi; Tomio Inoue


The Journal of Nuclear Medicine | 2015

Fever of unknown origin (FUO): evaluation of 50 cases with 18F-FDG PET/CT.

Yoshinobu Ishiwata; Keisuke Yoshida; Tomohiro Yoneyama; Tsuyoshi Kawano; Tomio Inoue


Society of Nuclear Medicine Annual Meeting Abstracts | 2013

Age-related regional changes of skeletal metabolism in women using 18F-fluoride PET

Seiji Kurata; Ukihide Tateishi; Kazuya Shizukuishi; Tomohiro Yoneyama; Ayako Hino; Hayato Kaida; Kiminori Fujimoto; Masatoshi Ishibashi; Tomio Inoue

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Tomio Inoue

University of Texas MD Anderson Cancer Center

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Ayako Hino

Yokohama City University

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Tomio Inoue

University of Texas MD Anderson Cancer Center

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