58 results match your criteria: "Kanazawa National Hospital[Affiliation]"
Arch Dis Child
March 1997
Department of Pediatrics, Kanazawa National Hospital, Japan.
A case is reported of dysgenetic male pseudohermaphroditism (DMPH) having Turner stigmata and 45,X/46,X+mar karyotype. The marker chromosome of this patient consisted of most if not all of the short arm, including the sex determining region of the Y chromosome. Although this karyotype is relatively common in Turner's syndrome and occasionally observed in mixed gonadal dysgenesis, DMPH is usually exemplified by a 46,XY karyotype except for one patient reported with 45,X/46,XY mosaicism.
View Article and Find Full Text PDFRyoikibetsu Shokogun Shirizu
September 1997
Department of Internal Medicine, Kanazawa National Hospital.
Ryoikibetsu Shokogun Shirizu
September 1997
Department of Internal Medicine, Kanazawa National Hospital.
Nihon Shokakibyo Gakkai Zasshi
January 1997
Department of Gastroenterology, Kanazawa National Hospital.
J Gastroenterol Hepatol
July 1996
Department of Surgery, Kanazawa National Hospital, Japan.
We present a case of portal-systemic encephalopathy due to a congenital splenorenal shunt. A 69 year old woman was admitted to hospital because of recurrent episodes of disturbed consciousness. The present episode had begun 3 months prior to admission.
View Article and Find Full Text PDFSurg Today
March 1997
Department of Surgery, Kanazawa National Hospital, Japan.
We report herein what to our knowledge is the first documented case of a malignant granular cell tumor of the stomach. A 64-year-old woman was admitted to our hospital for investigation of gastric submucosal tumor. Endoscopy disclosed a large hemispherical mass located on the lesser curvature at the gastric antrum with a normal mucosal surface, and computed tomography (CT) revealed a solid tumor about 7 cm in diameter with clear margins.
View Article and Find Full Text PDFHorm Res
November 1996
Department of Internal Medicine, Kanazawa National Hospital, Japan.
A 51-year-old male was admitted to our hospital because of diabetic ketoacidosis. His symptoms were promptly improved with intensive insulin therapy, but his plasma glucagon immunoreactivity measured by the OAL-123 radioimmunoassay (RIA) system showed persistently high values (3,090-3,210 pg/ml). A computed tomographic scan, abdominal angiography and endoscopic examination of his gastrointestinal tract showed no evidence of glucagonoma.
View Article and Find Full Text PDFJ Pediatr
November 1995
Department of Pediatrics, Kanazawa National Hospital, Japan.
We observed the sequential changes in serum thyroid hormones and thyroid-stimulating hormone receptor antibodies in an infant born at 30 weeks of gestation to a mother with florid Graves disease. Transient central hypothyroidism caused by pituitary suppression was observed after the resolution of peripheral thyrotoxicosis induced by thyroid-stimulating antibody. Central hypothyroidism became overt when the suppression of the pituitary gland after fetal thyrotoxicosis was combined with weak activity of thyroid-stimulating antibody after birth.
View Article and Find Full Text PDFNihon Rinsho
August 1995
Department of Internal Medicine, Kanazawa National Hospital.
Renal arterial disease-induced tubulo-interstitial lesions described in this chapter include benign arterio- and/or arteriolo-sclerotic and malignant nephrosclerosis, renal infarction and renal cortical necrosis. In these conditions renal glomeruli as well as tubules are always involved, and consequent loss of nephrons, or renal parenchyma results in interstitial fibrotic changes. The parenchymal lesions have a spectrum from slowly progressive atrophy and loss to necrosis of abrupt onset and disappearance of glomeruli and tubules.
View Article and Find Full Text PDFNihon Kyobu Shikkan Gakkai Zasshi
December 1994
Division of Pulmonary Medicine, Kanazawa National Hospital, Japan.
A 23-year-old man was admitted with a persistent high-grade fever of 20 days duration. Chest roentgenogram showed diffuse miliary shadows in both lung fields, highly suggestive of miliary tuberculosis. Sputum, gastric juice, and bronchoalveolar lavage fluid did not, however, reveal acid-fast bacilli on smears.
View Article and Find Full Text PDFJ Cardiovasc Surg (Torino)
December 1994
Division of Cardiovascular Surgery, Kanazawa National Hospital, Japan.
The internal thoracic artery (ITA), as well as aorto-coronary by-pass grafts, has been used for widely coronary artery by-pass grafting. Intra-aortic balloon pumping (IABP) is the first choice for left ventricular support when low output syndrome occurs during coronary artery by-pass surgery. However, the effect of diastolic augmentation by IABP may vary to the type of grafts.
View Article and Find Full Text PDFJ Gastroenterol
October 1994
Department of Internal Medicine, Kanazawa National Hospital, Japan.
An aberrant hepatic duct directly connected to the main pancreatic duct with anomalous arrangement of the pancreato-biliary ductal system is reported here, the first report of such a case, to our knowledge. A 53-year-old woman was admitted to our hospital because of cholecystolithiasis with abdominal pain in the right upper quadrant. Endoscopic retrograde cholangiopancreatography (ERCP) showed that an aberrant hepatic duct, which independently drained the right posterior segment of the liver, connected to the main pancreatic duct at a high insertion site distal to the sphincter area of the major papilla.
View Article and Find Full Text PDFHinyokika Kiyo
August 1994
Department of Urology, Kanazawa National Hospital.
The coincidence of renal cell carcinoma and renal angiomyolipoma in tuberous sclerosis is extremely rare, although the coexistence of tuberous sclerosis and renal angiomyolipoma is well recognized. A case of bilateral renal angiomyolipomas and left renal cell carcinoma in a patient with tuberous sclerosis is reported. A 40-year-old male was referred to our hospital for further evaluation and treatment of left flank masses.
View Article and Find Full Text PDFActa Paediatr Jpn
February 1994
Department of Pediatrics, Kanazawa National Hospital, Japan.
Intestinal malrotation presenting beyond the neonatal period is associated with a multiplicity of symptoms, which are often non-specific and, consequently, are associated with delays in diagnosis. Pseudo-Bartter's syndrome, which mimics the manifestations of Bartter's syndrome, can be caused by a severe chloride deficiency secondary to vomiting, diarrhea, perspiration, diuretic abuse and so on. We describe a 6 year old boy who had been admitted to hospital three times during the preceding year.
View Article and Find Full Text PDFNihon Kyobu Geka Gakkai Zasshi
November 1993
Department of Cardiovascular Surgery, Kanazawa National Hospital, Japan.
We report a patient of ventricular septal defect associated with a vegetations on the tricuspid valve and a perforation of the aortic cusp caused by infective endocarditis. Antibiotics could not relieve the high fever of this patient, and disseminated intravascular coagulation caused by sepsis and two-sided heart failure developed. She underwent extended tricuspid valve excision, aortic valve replacement and VSD closure during the active stage.
View Article and Find Full Text PDFNihon Jinzo Gakkai Shi
October 1993
Department of Internal Medicine, Kanazawa National Hospital, Japan.
It is not certain whether the life expectancy of patients with membranous nephropathy is shorter than that of an age-matched healthy population. Forty-one patients (21 males, 20 females) aged between 16 and 70 years (average age: 33.3 years) were followed for 20 years.
View Article and Find Full Text PDFKyobu Geka
September 1993
Department of Cardiovascular Surgery, Kanazawa National Hospital, Japan.
The thoracic sympathectomy was performed with standard laparoscopic and urologic equipment. After intubation, the patient was placed in a half sitting position. A Surgineedle was introduced into the pleural cavity through a 1 cm incision at the intercostal space between the first and second rib.
View Article and Find Full Text PDFIntern Med
May 1993
Department of Cardiology, Kanazawa National Hospital, Japan.
A patient with a history of adrenocortical carcinoma presented with massive pericardial effusion and a giant pericardial mass. Death resulted from cardiac tamponade. At autopsy a large necrotic mass was histologically similar to the original adrenocortical carcinoma.
View Article and Find Full Text PDFHinyokika Kiyo
October 1992
Department of Urology, Kanazawa National Hospital.
A study of bladder function was performed on 106 patients with benign prostatic hyperplasia (BPH), 21 of whom had cerebrovascular disease (CVD). The incidence of overactive bladder in 21 patients with CVD was 57% and was significantly higher than the 25% in 86 patients without CVD. The incidence of cases having residual urine of over 100 ml, was in the order of low compliance bladder, overactive bladder and normal bladder.
View Article and Find Full Text PDFHinyokika Kiyo
September 1992
Department of Urology, Kanazawa National Hospital.
The relationship between pathological spreading factors (T3,4 V+, N+, M+) and tumor size was studied in 45 patients with renal cell carcinoma during the past 10 years from 1982. The incidence of having one or more factors was 0% for the 17 tumors smaller than 5 cm, but 75% for the 28 tumors over 5 cm. The mean diameter of the tumors having a T, V, N or M factor was significantly larger than that of tumors having no factor (T1,2V0N0M0).
View Article and Find Full Text PDFHinyokika Kiyo
September 1992
Department of Urology, Kanazawa National Hospital.
We report the results of a comparative study on the clinical efficacy of the single use of distigmine bromide and its combined use with prazosin hydrochloride in the treatment of benign prostatic hypertrophy. The single use and combined use groups were administered 10 mg/day of distigmine bromide and the same with 1 mg/day of prazosin hydrochloride for a period of 8 weeks respectively. In the single administration group, marked improvement was found in one patient (9%), moderate improvement in 4 patients (36.
View Article and Find Full Text PDFNihon Jinzo Gakkai Shi
June 1992
Department of Internal Medicine, Kanazawa National Hospital.
In an attempt to clarify the indication and efficacy of the methylprednisolone pulse therapy (1000 mg x 3 times) for rapidly progressive glomerulonephritis (RPGN), 3 patients with the disease were carefully followed and the clinical course during and after the treatment were precisely analysed. According to the declination rate of reciprocals of serum creatinine (1/Cr), one patient were divided into the acute type (-1.00 x 10(-2) dl/mg/day or less) and the others into the subacute type (more than -1.
View Article and Find Full Text PDFHinyokika Kiyo
November 1991
Department of Urology, Kanazawa National Hospital.
The clinical effectiveness and safety of terodiline hydrochloride and clenbuterol hydrochloride were studied on 51 patients with neurogenic bladder, stress incontinence, unstable bladder and others, the chief complaints of which were urinary frequency or urinary incontinence. Overall improvement was graded as marked in 6 patients (11.8%), moderate in 20 patients (39.
View Article and Find Full Text PDFHinyokika Kiyo
October 1991
Department of Urology, Kanazawa National Hospital.
Cystometry and urethral pressure profile were determined in 41 patients (29 males and 12 females) with voiding disorders resulting from cerebrovascular accidents within one year after the episode. By clinical symptoms, they were classified into 3 groups, urge incontinence (14 patients, 34%), pollakisuria (10 patients, 24%) and dysuria (17 patients, 41%). Cystometrogram were classified into 3 types, hyperactive bladder (31 patients, 76%), normal bladder (5 patients, 12%) and hypoactive bladder (5 patients, 12%).
View Article and Find Full Text PDFNihon Jinzo Gakkai Shi
August 1991
Department of Internal Medicine, Kanazawa National Hospital, Japan.
In order to estimate the effects of methylprednisolone pulse therapy on progressive IgA nephropathy, clinical parameters in eight patients with the disease were compared between before and after the therapy. In this study progressive IgA nephropathy was defined as follows; 24 hour urinary protein excretion was (++) or more and renal biopsy carried out just before the therapy revealed crescents, inevitably including cellular crescents, in 10% or more glomeruli observed. Methylprednisolone 1000 mg a day was intravenously administered for three consecutive days and the therapy was repeated with an interval of 4 days.
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