2.Results of Mass Gastric Examination Conducted by the Nagano Prefectural Welfare Federation of Agricultural Cooperatives
Zenji Shimizu ; Kenji Usui ; Shigenobu Terashima ; Yoshio Takahashi ; Yoshimaru Sugiyama ; Tsutomu Fujita ; Kunihiro Oguchi ; Hajime Fushimi ; Etsuji Sano ; Takao Suzuki ; Takeshi Okada
Journal of the Japanese Association of Rural Medicine 1983;31(5):744-752
In order to carry out mass examination for detection of stomach ailments effectively and improve screening accuracy, the Nagano Prefectural Welfare Federation of Agricultural Cooperatives, with its mass gastric examination committee as a driving force, has made every endeavor in close collaboration with Federation-affiliated hospitals.
The ratio of those receiving detailed examination to the total number of those who have undergone mass screenings, and the detection ratio of gastric cancer cases, especially those in early stages, have increased steadily over the past years.
This is due in the main to untiring effort exerted by public health nurses and other persons concerned with health problems.
However, the results of X-ray examination made on the basis of the diagnostic standards prepared by the Federation show that there is much need of improving examiners' ability to read mass miniature radiographs correctly.
3.Myxopapillary Ependymoma of the Cauda Equina in a 5-Year-Old Boy.
Masashi UEHARA ; Jun TAKAHASHI ; Keijiro MUKAIYAMA ; Shugo KURAISHI ; Masayuki SHIMIZU ; Shota IKEGAMI ; Toshimasa FUTATSUGI ; Kenji SANO ; Kazuhiro HONGO ; Hiroyuki KATO
Asian Spine Journal 2014;8(6):846-851
Myxopapillary ependymoma in childhood typically occurs in the central nervous system. There are few surgical cases of myxopapillary ependymoma of the cauda equina in children. We report a case of myxopapillary ependymoma of the cauda equina in a 5-year-old boy, who presented with leg pain and abnormal gait. Subtotal resection surgery was performed. Following the subtotal tumor resection, follow-up magnetic resonance imaging evaluation showed a recurrent tumor. As a result, we performed a second subtotal tumor resection and followed with postoperative radiation therapy. No further evidence of the disease has been noted elsewhere in the patient in over ten years of follow-up. Myxopapillary ependymoma of the cauda equina in a young boy was improved by subtotal tumor resection and postoperative radiation therapy.
Cauda Equina*
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Central Nervous System
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Child
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Child, Preschool*
;
Ependymoma*
;
Follow-Up Studies
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Gait
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Humans
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Leg
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Magnetic Resonance Imaging
;
Male
4.Mice-lacking LMP2, immuno-proteasome subunit, as an animal model of spontaneous uterine leiomyosarcoma.
Takuma HAYASHI ; Akiko HORIUCHI ; Kenji SANO ; Nobuyoshi HIRAOKA ; Yae KANAI ; Tanri SHIOZAWA ; Susumu TONEGAWA ; Ikuo KONISHI
Protein & Cell 2010;1(8):711-717
Uterine tumors are the most common type of gynecologic neoplasm. Uterine leiomyosarcoma (LMS) is rare, accounting for 2% to 5% of tumors of the uterine body. Uterine LMS develops more often in the muscle tissue layer of the uterine body than in the uterine cervix. The development of gynecologic tumors is often correlated with female hormone secretion; however, the development of uterine LMS is not substantially correlated with hormonal conditions, and the risk factors are not yet known. Radiographic evaluation combined with PET/CT can be useless in the diagnosis and surveillance of uterine LMS. Importantly, a diagnostic biomarker, which distinguishes malignant LMS and benign tumor leiomyoma (LMA) is yet to be established. Accordingly, it is necessary to analyze risk factors associated with uterine LMS in order to establish a method of treatment. LMP2-deficient mice spontaneously develop uterine LMS, with a disease prevalence of ∼40% by 14 months of age. It is therefore of interest whether human uterine LMS shows a loss of LMP2 expression. We found LMP2 expression is absent in human LMS, but present in human LMA. Therefore, defective LMP2 expression may be one of the risk factors for LMS. LMP2 is potentially a diagnostic biomarker for uterine LMS, and gene therapy with LMP2-encording DNA may be a new therapeutic approach.
Animals
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Biomarkers, Tumor
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biosynthesis
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genetics
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Cysteine Endopeptidases
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biosynthesis
;
genetics
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Down-Regulation
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Female
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Gene Deletion
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Humans
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Interferon Regulatory Factor-1
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biosynthesis
;
genetics
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Leiomyoma
;
metabolism
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Leiomyosarcoma
;
diagnosis
;
genetics
;
metabolism
;
Mice
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Mice, Knockout
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Proteasome Endopeptidase Complex
;
metabolism
;
Uterine Neoplasms
;
diagnosis
;
genetics
;
metabolism
5.A Case of Brugada Syndrome Treated With Percutaneous Epicardial Catheter Ablation
Masahiro OGAWA ; Yoshiyuki HYOUDOU ; Masayuki OKIJIMA ; Hirotaka INOUE ; Kouji KONDOU ; Yuki FUJII ; Atsuya SAKAIDE ; Keisuke TSUJIKAWA ; Kazuyoshi NISHIYAMA ; Ryouta TANI ; Izumi OHTA ; Mizuki ENDOU ; Kimitoshi SANO ; Kenji NAKAMAE ; Shinji KANEKO ; Masaya FUJITA ; Yousuke TATAMI ; Osamu KAWAGUCHI
Journal of the Japanese Association of Rural Medicine 2020;69(4):385-
This case report describes our first experience performing percutaneous epicardial catheter ablation for Burugada syndrome in our hospital. We describe the good results achieved in this case. The patient was a man in his 30s with no remarkable medical history. However, his family history was notable for the sudden death of his grandfather at age 37 years and his father at age 27 years. While asleep, the patient experienced convulsions and lost consciousness. During emergency transportation, defibrillation was performed 7 times by the ambulance crew. When the patient arrived at our hospital, sinus rhythm was observed on ECG. During resuscitation, Burugada syndrome was diagnosed based on ECG findings. On hospital day 6, an internal cardioverter defibrillator was implanted. After discharge, the defibrillator operated 10 times, so we opted for ablation treatment. Fractionated potential of over 150 ms was confirmed in the right ventricular outflow tract. A low voltage zone of <1 mV could be mapped, and the same site was cauterized a total of 46 times. As a result, ST segment amplitude decreased significantly in lead V1 on ECG. Percutaneous epicardial catheter ablation performed with reference to Nademanee’s report achieved good results in this case of Burugada syndrome.