Kiminori Fujimoto

Prof. Kiminori Fujimoto

Kurume University, Kurume, Japan

Research Focus & Metrics

Academic Career Length

30Years (1997-Present)

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

Representative Publications

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7 August 2011 in European Radiology
Verified
Journal Article
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KFKiminori Fujimoto
Kiminori Fujimoto
HTHiroyuki Taniguchi
Hiroyuki Taniguchi
TJTakeshi Johkoh
Takeshi Johkoh
YKYasuhiro Kondoh
Yasuhiro Kondoh
KIKazuya Ichikado
Kazuya Ichikado
NMNestor L. Müller
Nestor L. Müller

1 March 2011 in Radiology
Verified
Journal Article
Closed access
KFKiminori Fujimoto
Kiminori Fujimoto
TTTatsuyuki Tonan
Tatsuyuki Tonan
SASanae Azuma
Sanae Azuma
MKMasayoshi Kage
Masayoshi Kage
ONOsamu Nakashima
Osamu Nakashima
AQAliya Qayyum
Aliya Qayyum
Our preliminary data suggest that mean and entropy apparent diffusion coefficient values might be helpful for predicting pathologic hepatic fibrosis stage and inflammatory activity grade in patients with chronic hepatitis C. PurposeTo determine whether mean and entropy apparent diffusion coefficient (ADC) values obtained at diffusion-weighted (DW) magnetic resonance (MR) imaging can help detect and stage histopathologic liver fibrosis and grade inflammation activity in patients with chronic hepatitis C.Materials and MethodsThis retrospective study was approved by the institutional review board, and the requirement for informed consent was waived. The study included 55 patients with focal hepatic lesions and either chronic hepatitis C (n = 43) or normal hepatic function (control subjects) (n = 12). Mean and entropy of volume histograms were generated in four cubic regions of interest placed in the right hepatic lobe of ADC map images, which were obtained at echo-planar DW MR imaging (gradient factor b values of 0 and 1000 sec/mm2). These two parameters (mean and entropy ADC) were compared by using METAVIR histopathologic liver fibrosis and inflammatory activity scores. Statistical analysis was performed with the Kruskal-Wallis...

1 January 2007 in American Journal of Roentgenology
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Journal Article
Closed access
RKRei Kono
Rei Kono
KFKiminori Fujimoto
Kiminori Fujimoto
HTHiroshi Terasaki
Hiroshi Terasaki
NMNestor L. Müller
Nestor L. Müller
SKSeiya Kato
Seiya Kato
STShinzo Takamori
Shinzo Takamori
OBJECTIVE. The purpose of this study was to compare the dynamic contrast-enhanced MRI enhancement characteristics of malignant and benign solitary pulmonary nodules.MATERIALS AND METHODS. The characteristics of 202 solitary pulmonary nodules (diameter, 1-3 cm; 144 cases of primary lung cancer, 31 cases of focal organizing pneumonia, 15 tuberculomas, 12 hamartomas) were reviewed retrospectively. In all cases dynamic MR images were obtained before and 1, 2, 3, 4, 5, 6, and 8 minutes after bolus injection of gadopentetate dimeglumine. Maximum enhancement ratio, time at maximum enhancement ratio, slope of time-enhancement ratio curves, and washout ratio were assessed. Statistical analyses were performed with the Kruskal-Wallis test with Bonferroni correction, chi-square test, and receiver operating characteristic curves.RESULTS. For 122 (85%) of 144 primary lung cancers, time at maximum enhancement ratio was 4 minutes or less. For all tuberculomas and hamartomas, time at maximum enhancement ratio was greater ...

1 March 2015 in Respiratory Investigation
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Journal Article
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MTMorihiro Tajiri
Morihiro Tajiri
MOMasaki Okamoto
Masaki Okamoto
KFKiminori Fujimoto
Kiminori Fujimoto
TJTakeshi Johkoh
Takeshi Johkoh
JOJunya Ono
Junya Ono
THTomoaki Hoshino
Tomoaki Hoshino

6 December 2013 in Oncology Reports
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Journal Article
Open access
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KFKiminori Fujimoto
Kiminori Fujimoto
MHMasaki Hara
Masaki Hara
NTNoriyuki Tomiyama
Noriyuki Tomiyama
MKMasahiko Kusumoto
Masahiko Kusumoto
FSFumikazu Sakai
Fumikazu Sakai
YFYoshitaka Fujii
Yoshitaka Fujii
There is no existing worldwide published method for mediastinum compartment classification based on transverse section images for the differential diagnosis of mediastinal tumors. Herein, we describe a new method for anatomic mediastinal compartment classification using transverse section computed tomography (CT) images and the use of this method to classify mediastinal lesions, and thus evaluate whether the method is sufficiently user-friendly and useful. In a publication of the Japanese Association for Research on the Thymus (JART), we proposed the following four mediastinal compartments based on transverse CT images: superior portion of mediastinum, anterior mediastinum (prevascular zone), middle mediastinum (peri-tracheoesophageal zone), and posterior mediastinum (paravertebral zone). In the present study, we retrospectively analyzed 445 pathologically proven mediastinal mass lesions, and categorized them into the proposed four compartments by consensus reading. Mass lesions were classified into compartments based on the location of the lesion centroid, and each lesion was satisfactorily categorized into a compartment. Almost all thymic epithelial tumors (99%, 244/246), all 24 thymic malignant lymphomas and a majority of germ cell neoplasms (93%, 54/58) were classified as being in the anterior mediastinum compartment. The majority of intrathoracic goiters (82%, 14/17) were categorized as being in the superior portion of the mediastinum compartment. Approximately two-thirds of mass lesions in the middle mediastinum were cysts, including foregut and pericardial cysts. Approximately 80% of 37 mass lesions in the posterior mediastinum were neurogenic tumors. Correspondingly, 29 of the 49 neurogenic tumors (60%) were categorized as being in the posterior mediastinum, while 10 (20%) were in the superior portion of the mediastinum, 4 (8%) in the anterior mediastinum, and 6 (12%) in the middle mediastinum. Our findings showed that the newly proposed mediastinal compartment classification using transverse images appears to be user-friendly enough for practical clinical application and may be helpful in differential diagnoses.

1 June 2003 in Radiology
Verified
Journal Article
Closed access
KFKiminori Fujimoto
Kiminori Fujimoto
TAToshi Abe
Toshi Abe
NMNestor L. Müller
Nestor L. Müller
HTHiroshi Terasaki
Hiroshi Terasaki
SKSeiya Kato
Seiya Kato
NHNaofumi Hayabuchi
Naofumi Hayabuchi
To correlate the findings at contrast material-enhanced dynamic magnetic resonance (MR) imaging of small peripheral pulmonary carcinomas with tumor vascularity and prognosis.Ninety-four patients with small peripheral pulmonary carcinomas who underwent surgical resection were examined retrospectively. Pathologic specimens were stained with hematoxylin-eosin and elastin-van Gieson. CD34 and vascular endothelial growth factor (VEGF) were assessed immunohistochemically. Delineated CD34-positive cells were counted as microvessels. Dynamic MR imaging was performed prior to and at 1, 2, 3, 4, 5, 6, and 8 minutes after injection of a bolus of gadopentetate dimeglumine. The two observers reviewed all images, and two pathologists performed all histologic analyses; a decision was determined with consensus. The maximum enhancement ratio (MER), the time lapse between the completion of the injection and the point of maximum signal intensity (Tmax), the washout ratio, and the slope value of the time-signal intensity curve were correlated with the microvessel density. VEGF-positive and VEGF-negative tumors were compared. All statistical analyses were performed by using nonparametric methods.The MER and the slope value were positively correlated, and the Tmax was negatively correlated (Spearman rank test, P <.0001, all comparisons) with the microvessel counts. The distribution of elastic and collagen fibers correlated with the washout ratio (Kruskal-Wallis test, P <.001). There was a statistically significant difference between the slope value of VEGF-positive tumors and that of VEGF-negative tumors (Mann-Whitney U test, P <.0001). Patients with VEGF-positive tumors had a significantly shorter overall survival than did those with VEGF-negative tumors (log-rank test, P <.0001).Dynamic MR imaging findings correlate with tumor vascularity and may be helpful in the prediction of prognosis.