Hisashi Kidani
Kanazawa University
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Featured researches published by Hisashi Kidani.
Pancreas | 1993
Tokio Wakabayashi; Norio Sawabu; Yasuhiro Takemori; Yoshitake Satomura; Hisashi Kidani; Hideki Ohta; Hiroyuki Watanabe; Osamu Yamakawa; Hirokazu Takahashi; Kishichiroh Watanabe; Fumio Konishi
This study evaluated the diagnostic significance of concentrations of the cancer-associated carbohydrate antigen CA 19–9 in pure pancreatic juice (PPJ) collected by endoscopic cannulation. We also attempted to elucidate the features and source of the increased CA 19–9 concentration found in the pancreatic juice of patients with chronic pancreatitis (CP) by means of immunohistochemical staining. The mean output as well as the mean concentration of CA 19–9 in each of the four fractions collected was highest in patients with pancreatic cancer (PC) and also was elevated significantly in patients with CP compared with controls. However, CA 19–9 concentrations were not elevated in patients with cholecystolithiasis. When the cutoff value was set as the mean concentration + 2SD of the controls, significantly elevated concentrations of CA 19–9 were found in the third fraction (secretory phase) in 90% of the patients with PC and 66% of the patients with CP. Immunohistochemical staining revealed that CA 19–9 was expressed more widely in the ductal cells of CP tissues than in those of normal pancreatic (NP) tissues, with CP tissue showing more CA 19–9-positive ductal cells per area than NP tissues. In NP tissue, CA 19–9 was localized to the apical surface and supranuclear regions (apical type) in all the ductal cells stained by the antigen, while ∼50% of cases with CP exhibited a cytoplasmic pattern showing a loss of polarity of the antigen expression. Moreover, this cellular localization pattern was more pronounced in the small ducts that had proliferated and aggregated following the destruction of lobules in CP. These results indicate that although increased concentrations of CA 19–9 in PPJ have no cancer specificity, measurement of CA 19–9 in PPJ can be used as a sensitive marker for some pancreatic disorders, and higher CA 19–9 concentrations in the pancreatic juice of patients with CP may reflect the strong expression of CA 19–9 in the proliferating small ducts associated with CP.
Gastroenterologia Japonica | 1985
Norio Sawabu; Tokio Wakabayashi; Kenji Ozaki; Daishu Toya; Manabu Yoneshima; Hisashi Kidani; Nobu Hattori; Masaru Ishii
SummaryThe presence of specific gamma-glutamyl transpeptidase isoenzyme (γ-GTPI) and variant alkaline phosphatase (VAALP) were concurrently determined, and levels of basic fetoprotein (BFP) and carcinoembryonic antigen (CEA) in addition to α-fetoprotein (AFP) were measured in 144 hepatocellular carcinoma (HCC) patients in order to evaluate the diagnostic value of these tumor markers with respect to AFP-low or -negative patients and the tumor stage.Serum AFP levels below 400 ng/ml, commonly seen in sera of hepatobiliary diseases other than HCC, were noted in 42% of the patients. The diagnostic usefulness was increased by combination assay of these markers except for CEA. A definitive diagnosis of HCC could be made in 78% of the patients by a combination of γ-GTPI, VAALP and AFP. Moreover, a diagnosis of malignancy could be made in 87% of cases by the inclusion of BFP. The prevalence of BFP and CEA increased in proportion to the tumor stage, whereas that of AFP and γ-GTPI were independent of stage and were high even in patients in comparatively early stages. Furthermore, secreting type markers such as AFP and γ-GTPI were relatively useful for diagnosis of HCC when the lesions were still small.
Gastroenterologia Japonica | 1986
Norio Sawabu; Yasuhiro Takemori; Daishu Toya; Manabu Yoneshima; Hisashi Kidani; Yoshitake Satomura; Hideki Ohta; Nobu Hattori
SummaryIn order to elucidate the factors affecting the serum levels of CA 19-9, we analyzed sera of 79 patients with pancreatic cancer and 169 with non-malignant diseases, chiefly consisting of hepatobiliary and pancreatic diseases. Serum CA 19-9 values in patients with pancreatic cancer had no relation to the location of the tumor or presence of jaundice. Similarly, no tendency was observed as to the location and size of tumor or to the grade of differentiation in 12 CA 19-9-negative patients with pancreatic cancer. Serum levels of CA 19-9 in patients with cholelithiasis complicated by cholangitis frequently showed markedly high values, but then rapidly normalized in parallel with the subsiding of inflammation. The behaviour of serum CA 19-9 showed little relation to renal or hepatic failures or to intrahepatic cholestasis. However, slightly elevated levels of the antigen were found in more than half of those patients with fulminant hepatitis showing massive necrosis. In chronic pancreatitis, the prevalence was only 8%; however, an increase was observed at the time of exacerbation in 2 of 5 positive patients. There was hardly any increase in serum levels of CA 19-9 after endoscopic retrograde cholangiopancreatography (ERCP), although serum levels of pancreatic enzymes rose after ERCP in almost all patients. Thus, it appears that CA 19-9 does not easily escape into the bloodstream, unlike pancreatic enzymes.
International Journal of Pancreatology | 1994
Hideki Ohta; Norio Sawabu; Yasuhiro Takernori; Hisashi Kidani; Tokio Wakahayashi; Yoshitake Satomura; Hiroyuki Watanabe; Yoshiharu Motoo; Takashi Okai; Hirokazu Takahashi
SummaryThe diagnostic significance of measuring sialylated stage-specific embryonic antigen-1 (SLX) in pure pancreatic juice was evaluated in 20 patients with pancreatic cancer, 43 with chronic pancreatitis, 13 with cholecystolithiasis, and 15 control individuals. Four fractions of pure pancreatic juice were collected sequentially from the pancreatic duct by endoscopic cannulation. The SLX levels in all four fractions of pure pancreatic juice were significantly higher in patients with pancreatic cancer than in controls. On the other hand, patients with chronic pancreatitis or cholecystolithiasis did not have SLX levels that significantly differed from those of controls in any fraction. When the cut-off value was set as the mean concentration + 2 times the standard deviation of the control values, the positive rates of SLX in the first fraction (washout phase) and the third fraction (secretory phase) of pure pancreatic juice from pancreatic cancer were 55% (11/20) and 40% (8/20), respectively. Although the false positive rates in the first fraction were high in chronic pancreatitis (30%) and cholecystolithiasis (31%), such high SLX levels in the third fraction were found only in one (2%) patient with chronic pancreatitis and in one (8%) with cholecystolithiasis. The specificities of the test for pancreatic cancer in the first fraction and the third fraction were 70% (39/56) and 96% (54/56), respectively. These results indicate that the measurement of SLX in the third fraction of pure pancreatic juice is useful as a specific marker for pancreatic cancer.
Journal of Computer Assisted Tomography | 1991
Yasuhiro Kawamori; Osamu Matsui; Kiyohide Kitagawa; Masumi Kadoya; Teruo Yamahana; Tsutomu Takashima; Hisashi Kidani; Shinji Masuda; Yasuni Nakanuma
We report a case of segmental hepatic iron deposition in the parenchyma peripheral to a tumor-thrombosed intrahepatic portal vein. On MR imaging, especially fast low-angle shot image, the liver parenchyma was demonstrated as a hypointense area with segmental and wedge-shaped configuration. Absence of portal blood flow may cause such segmental hepatic iron deposition.
Digestive Endoscopy | 1990
Yasuhiro Takemori; Norio Sawabu; Hideki Ohta; Yoshitake Satomura; Hiroyuki Watanabe; Osamu Yamakawa; Hiroyasu Kawakami; Hisashi Kidani; Hirokazu Takahashi; Tokio Wakabayashi
Abstract: This study was undertaken to elucidate the diagnostic significance of the measurement of a cancer‐associated carbohydrate antigen, NCC‐ST‐439 (ST‐439), in pure pancreatic juice collected by endoscopic cannulation, chiefly from patients with pancreatic diseases.
Journal of Clinical Gastroenterology | 1992
Takashi Okai; Norio Sawabu; Yasuhiro Takemori; Hideki Ohta; Yoshiharu Motoo; Hisashi Kidani
Kanzo | 1988
Kazuo Notsumata; Masashi Unoura; Fumiaki Matsushita; Mitsuhiro Terada; Hisashi Kidani; Yoshiharu Motoo; Kenichi Kobayashi; Nobu Hattori; Yasuni Nakanuma; Mikio Kumagai
Kanzo | 1984
Manabu Yoneshima; Norio Sawabu; Daishu Toya; Hisashi Kidani; Takashi Okai; Kenji Ozaki; Tokio Wakabayashi; Yasuhiro Kato; Kenichi Kobayashi; Nobu Hattori; Masumi Kadoya; Masayuki Suzuki; Chikara Takashima
Kanzo | 1994
Mitsuro Kato; Hidero Ogino; Kyosuke Kaji; Hiroshi Kawai; Masayuki Yanagi; Eiki Matsushita; Takeshi Urabe; Shuichi Kaneko; Masashi Unoura; Kenichi Kobayashi; Yasuni Nakanuma; Hisashi Kidani