Kiyohisa Kamimura

Dr. Kiyohisa Kamimura

Department of Radiology, Kagoshima University Graduate School of Medical and Dental Sciences
orcid

Research Focus & Metrics

Academic Career Length

14Years (2013-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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5 November 2013 in Journal of Magnetic Resonance Imaging
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Journal Article
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KKKiyohisa Kamimura
Kiyohisa Kamimura
YFYoshihiko Fukukura
Yoshihiko Fukukura
TYTomohide Yoneyama
Tomohide Yoneyama
KTKoji Takumi
Koji Takumi
ATAkihiro Tateyama
Akihiro Tateyama
MNMasayuki Nakajo
Masayuki Nakajo

19 October 2018 in Japanese Journal of Radiology
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Journal Article
Closed access
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KKKiyohisa Kamimura
Kiyohisa Kamimura
MNMasanori Nakajo
Masanori Nakajo
TYTomohide Yoneyama
Tomohide Yoneyama
KTKoji Takumi
Koji Takumi
YKYuichi Kumagae
Yuichi Kumagae
TYTakashi Yoshiura
Takashi Yoshiura

1 April 2014 in European Journal of Radiology
Verified
Journal Article
Closed access
YFYoshihiko Fukukura
Yoshihiko Fukukura
KTKoji Takumi
Koji Takumi
MHMichiyo Higashi
Michiyo Higashi
SSShinchi Shinchi
Shinchi Shinchi
KKKiyohisa Kamimura
Kiyohisa Kamimura
ATAkihiro Tateyama
Akihiro Tateyama

8 August 2023 in Cancer Imaging
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Journal Article
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KKKiyohisa Kamimura
Kiyohisa Kamimura
YKYoshiki Kamimura
Yoshiki Kamimura
TNTsubasa Nakano
Tsubasa Nakano
THTomohito Hasegawa
Tomohito Hasegawa
MNMasanori Nakajo
Masanori Nakajo
TYTakashi Yoshiura
Takashi Yoshiura
Background: This study was designed to investigate the use of time-dependent diffusion magnetic resonance imaging (MRI) parameters in distinguishing between glioblastomas and brain metastases. Methods: A retrospective study was conducted involving 65 patients with glioblastomas and 27 patients with metastases using a diffusion-weighted imaging sequence with oscillating gradient spin-echo (OGSE, 50 Hz) and a conventional pulsed gradient spin-echo (PGSE, 0 Hz) sequence. In addition to apparent diffusion coefficient (ADC) maps from two sequences (ADC50Hz and ADC0Hz), we generated maps of the ADC change (cADC): ADC50Hz − ADC0Hz and the relative ADC change (rcADC): (ADC50Hz − ADC0Hz)/ ADC0Hz × 100 (%). Results: The mean and the fifth and 95th percentile values of each parameter in enhancing and peritumoral regions were compared between glioblastomas and metastases. The area under the receiver operating characteristic curve (AUC) values of the best discriminating indices were compared. In enhancing regions, none of the indices of ADC0Hz and ADC50Hz showed significant differences between metastases and glioblastomas. The mean cADC and rcADC values of metastases were significantly higher than those of glioblastomas (0.24 ± 0.12 × 10−3mm2/s vs. 0.14 ± 0.03 × 10−3mm2/s and 23.3 ± 9.4% vs. 14.0 ± 4.7%; all p < 0.01). In peritumoral regions, no significant difference in all ADC indices was observed between metastases and glioblastomas. The AUC values for the mean cADC (0.877) and rcADC (0.819) values in enhancing regions were significantly higher than those for ADC0Hz5th (0.595; all p < 0.001). Conclusions: The time-dependent diffusion MRI parameters may be useful for differentiating brain metastases from glioblastomas.

3 August 2021 in Cancers
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Journal Article
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KKKiyohisa Kamimura
Kiyohisa Kamimura
MNMasanori Nakajo
Masanori Nakajo
MBManisha Bohara
Manisha Bohara
DNDaigo Nagano
Daigo Nagano
YFYoshihiko Fukukura
Yoshihiko Fukukura
Takashi YoshiuraTakashi Yoshiura
Takashi Yoshiura
Prediction of tumor consistency is valuable for planning transsphenoidal surgery for pituitary adenoma. A prospective study was conducted involving 49 participants with pituitary adenoma to determine whether quantitative pharmacokinetic analysis of dynamic contrast-enhanced magnetic resonance imaging (DCE-MRI) is useful for predicting consistency of adenomas. Pharmacokinetic parameters in the adenomas including volume of extravascular extracellular space (EES) per unit volume of tissue (ve), blood plasma volume per unit volume of tissue (vp), volume transfer constant between blood plasma and EES (Ktrans), and rate constant between EES and blood plasma (kep) were obtained. The pharmacokinetic parameters and the histologic percentage of collagen content (PCC) were compared between soft and hard adenomas using Mann–Whitney U test. Pearson’s correlation coefficient was used to correlate pharmacokinetic parameters with PCC. Hard adenomas showed significantly higher PCC (44.08 ± 15.14% vs. 6.62 ± 3.47%, p < 0.01), ve (0.332 ± 0.124% vs. 0.221 ± 0.104%, p < 0.01), and Ktrans (0.775 ± 0.401/min vs. 0.601 ± 0.612/min, p = 0.02) than soft adenomas. Moreover, a significant positive correlation was found between ve and PCC (r = 0.601, p < 0.01). The ve derived using DCE-MRI may have predictive value for consistency of pituitary adenoma.

11 August 2016 in American Journal of Neuroradiology
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Journal Article
Open access
PDF file
KKKiyohisa Kamimura
Kiyohisa Kamimura
MNM. Nakajo
M. Nakajo
YFYoshihiko Fukukura
Yoshihiko Fukukura
TIT. Iwanaga
T. Iwanaga
TST. Saito
T. Saito
Takashi YoshiuraTakashi Yoshiura
Takashi Yoshiura
BACKGROUND AND PURPOSE: DWI with conventional single-shot EPI of the pituitary gland is hampered by strong susceptibility artifacts. Our purpose was to evaluate the feasibility of intravoxel incoherent motion assessment by using DWI based on TSE of the normal anterior pituitary lobe. MATERIALS AND METHODS: The intravoxel incoherent motion parameters, including the true diffusion coefficient (D), the perfusion fraction (f), and the pseudo-diffusion coefficient (D*), were obtained with TSE-DWI in 5 brain regions (the pons, the WM and GM of the vermis, and the genu and splenium of the corpus callosum) in 8 healthy volunteers, and their agreement with those obtained with EPI-DWI was evaluated by using the intraclass correlation coefficient. The 3 intravoxel incoherent motion parameters in the anterior pituitary lobe were compared with those in the brain regions by using the Dunnett test. RESULTS: The agreement between TSE-DWI and EPI-DWI was moderate (intraclass correlation coefficient = 0.571) for D, substantial (0.699) for f', but fair (0.405) for D*. D in the anterior pituitary lobe was significantly higher than in the 5 brain regions (P < .001). The f in the anterior pituitary lobe was significantly higher than in the 5 brain regions (P < .001), except for the vermian GM. The pituitary D* was not significantly different from that in the 5 brain regions. CONCLUSIONS: Our results demonstrated the feasibility of intravoxel incoherent motion assessment of the normal anterior pituitary lobe by using TSE-DWI. High D and f values in the anterior pituitary lobe were thought to reflect its microstructural and perfusion characteristics.