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  <channel rdf:about="http://hdl.handle.net/10564/1545">
    <title>DSpace コレクション: 2001-10</title>
    <link>http://hdl.handle.net/10564/1545</link>
    <description>2001-10</description>
    <items>
      <rdf:Seq>
        <rdf:li rdf:resource="http://hdl.handle.net/10564/680" />
        <rdf:li rdf:resource="http://hdl.handle.net/10564/679" />
        <rdf:li rdf:resource="http://hdl.handle.net/10564/678" />
        <rdf:li rdf:resource="http://hdl.handle.net/10564/677" />
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    <dc:date>2026-04-10T15:40:46Z</dc:date>
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  <item rdf:about="http://hdl.handle.net/10564/680">
    <title>興味あるMRI所見と遅発性ジストニアを呈した精神分裂病の1例</title>
    <link>http://hdl.handle.net/10564/680</link>
    <description>タイトル: 興味あるMRI所見と遅発性ジストニアを呈した精神分裂病の1例
著者: 芳野, 浩樹; 森川, 将行; 平山, 智英; 大澤, 弘吉; 岸本, 年史; 飯田, 順三
抄録: Tardive dystonia is one of the extrapyramidal syndromes and occurs after &#xD;
prolonged treatment with neuroleptic medication. It consists of sustained muscle &#xD;
contractions, frequently causing twisting, repetitive movements and abnormal posture. &#xD;
We report a case of schizophrenia with tardive dystonia and unusual features on brain &#xD;
MRI. The patient (a 37-year-old single male) had been suffering from schizophrenia &#xD;
during the past 20 years. At age 28, he developed spasmodic movements of the upper &#xD;
limbs, torticollis and opisthotonus, and was diagnosed as having tardive dystonia. &#xD;
Dantrolene sodium therapy successfully alleviated his dystonia. At age 37, he &#xD;
discontinued neuroleptics by himself. As a result, he had a relapse and entered our &#xD;
psychiatric ward. His psychiatric symptoms were auditory hallucination, religious &#xD;
delusions, and psychomotor excitement. Also his lasting mild tardive dystonia had &#xD;
deteriorated. Brain MRI revealed multiple lacunar infarction, ischemic changes and brain &#xD;
atrophy. In this case, these MRI findings might be related to the development of tardive &#xD;
dystonia. Switching to low-potency neuroleptics alleviated the tardive dystonia. Various &#xD;
factors relate to tardive dystonia, and diagnostic imaging such as MRI might be &#xD;
necessary for schizophrenia with tardive dystonia.</description>
    <dc:date>2001-10-30T15:00:00Z</dc:date>
  </item>
  <item rdf:about="http://hdl.handle.net/10564/679">
    <title>RENOVASCULAR HYPERTENSION AND ERECTILE DYSFUNCTION SECONDARY TO POLYARTERITIS NODOSA : A CASE REPORT</title>
    <link>http://hdl.handle.net/10564/679</link>
    <description>タイトル: RENOVASCULAR HYPERTENSION AND ERECTILE DYSFUNCTION SECONDARY TO POLYARTERITIS NODOSA : A CASE REPORT
著者: Yamano, Shigeru; Kyoda, Yusuke; Shiiki, Hideo; Fujimoto, Takashi; Hashimoto, Toshio; Kitauchi, Takanori; Kagebayashi, Yoriaki; Hirao, Yoshihiko
抄録: We describe a patient with secondary hypertension and erectile &#xD;
dysfunction due to polyarteritis nodosa. A 30-year-old man was admitted because of &#xD;
hypertension and impotence. Blood pressure was 156/94 mm Hg, and was similar in both &#xD;
arms. Superficial sensation was diminished in the soles of the feet. Plasma renin activity &#xD;
was elevated. Intra-arterial digital subtraction angiography (DSA) of the renal arteries &#xD;
showed bilateral multiple microaneurysms in peripheral arterial branches between the &#xD;
interlobular and arcuate arteries of both kidneys. DSA of the internal iliac artery, the &#xD;
internal pudendal artery, and the hepatic artery also showed multiple microaneurysms, as &#xD;
well as focal stenoses. A diagnosis of organic (vascular) erectile dysfunction was made &#xD;
based on findings by the Rigi-scan (Dacomed Inc.). The patient, then, had polyarteritis &#xD;
nodosa presenting hypertension and erectile dysfunction.</description>
    <dc:date>2001-10-30T15:00:00Z</dc:date>
  </item>
  <item rdf:about="http://hdl.handle.net/10564/678">
    <title>A CASE OF MALIGNANT RENAL NEOPLASM WITH RHABDOID FEATURES IN AN ADULT</title>
    <link>http://hdl.handle.net/10564/678</link>
    <description>タイトル: A CASE OF MALIGNANT RENAL NEOPLASM WITH RHABDOID FEATURES IN AN ADULT
著者: Kumamoto, Hiromi; Ozono, Seiichiro; Tsujimoto, Sigehiro; Yoshii, Masato; Kitauchi, Takanori; Hosokawa, Yukinari; Mibu, Hisakazu; Kagebayashi, Yoriaki; Hirao, Yoshihiko; Ichijima, Kunio
抄録: We report a case of malignant neoplasm with rhabdoid features of the &#xD;
kidney in a 68 year old man. To our knowledge malignant rhabdoid tumor of the kidney &#xD;
(MRTK) has been limited to the pediatric age group. Malignant renal neoplasm &#xD;
similar to MRTK occurring in adults is very rare. However, there has been a &#xD;
recent review in which the authors found 23/480 cases of renal cell carcinoma (RCC) &#xD;
(4.7%) exhibiting rhabdoid features, all in adults. In the present case, examination of &#xD;
many sections of tumor-affected tissue revealed no sign of any other malignant tumor &#xD;
included RCC, so-called pure adult malignant rhabdoid tumor in the kidney. MRTK does &#xD;
not respond well to aggressive chemotherapy regimens and survival tends to be short. &#xD;
This patient remains alive with no metastasis and local recurrence more than 45 months &#xD;
from the operation without adjuvant therapy.</description>
    <dc:date>2001-10-30T15:00:00Z</dc:date>
  </item>
  <item rdf:about="http://hdl.handle.net/10564/677">
    <title>CYTOLOGIC CHARACTERISTICS OF A MALIGNANT PROLIFERATING TRICHILEMMAL CYST</title>
    <link>http://hdl.handle.net/10564/677</link>
    <description>タイトル: CYTOLOGIC CHARACTERISTICS OF A MALIGNANT PROLIFERATING TRICHILEMMAL CYST
著者: Ishida, Eiwa; Nakamura, Mitsutoshi; Konishi, Noboru; Matsunaga, Shigeo; Morishima, Hidekazu; Honda, Junko; Sekigawa, Susumu
抄録: The proliferating trichilemmal cyst (PTC)is a tumor that originates from &#xD;
hair follicles. It is almost always benign, but rare lesions have been reported with &#xD;
malignant potential. In the present case, the patient had a mass on the right side of her &#xD;
neck for a few years, which suddenly increased in size. Cytologic examination revealed &#xD;
many atypical squamous cells staining well with orange G and light green, suggestive of &#xD;
a squamous cell carcinoma. Total extirpation was performed under general anesthesia, &#xD;
gross pathology revealing a focally cystic tumor approximately 5 cm in diameter. The &#xD;
final diagnosis was malignant PTC from the characteristic features. We here report &#xD;
cytologic findings for this case with regional lymph node metastasis.</description>
    <dc:date>2001-10-30T15:00:00Z</dc:date>
  </item>
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