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    <title>DSpace コレクション: 2009-12</title>
    <link>http://hdl.handle.net/10564/1477</link>
    <description>2009-12</description>
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    <dc:date>2026-04-10T15:40:12Z</dc:date>
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  <item rdf:about="http://hdl.handle.net/10564/1105">
    <title>第129回奈良医学会 : 学会記事</title>
    <link>http://hdl.handle.net/10564/1105</link>
    <description>タイトル: 第129回奈良医学会 : 学会記事</description>
    <dc:date>2009-12-30T15:00:00Z</dc:date>
  </item>
  <item rdf:about="http://hdl.handle.net/10564/1104">
    <title>胆石イレウスの1例</title>
    <link>http://hdl.handle.net/10564/1104</link>
    <description>タイトル: 胆石イレウスの1例
著者: 中辻, 直之; 八倉, 一晃; 越智, 祥隆; 吉田, 英晃
抄録: Gallstone ileus is a rare complication of cholecystolithiasis. We report a &#xD;
case of gallstone ileus diagnosed preoperatively by abdominal computed tomography &#xD;
(CT). A 57-year-old female was admitted to our hospital due to epigastric pain and &#xD;
vomiting. She had a history of cholecystolithiasis. Abdominal plain X-ray showed niveau &#xD;
and abdominal CT showed the presence of calcification round in shape (20mm in &#xD;
diameter) in the small intestine and cholecystoduodenal fistula. Laparotomy was &#xD;
performed under a diagnosis of gallstone ileus with cholecystoduodenal fistula. At &#xD;
exploration, a stone packed in the ileum 50cm oral from the ileum end was found and a &#xD;
wall-thickened gallbladder was found firmly adherent at the duodenum. We removed the &#xD;
impacted stone from the intestine and performed cholecystectomy and placed an omental &#xD;
patching after trimming the wall of the duodenum to close the cholecystoduodenal fistula. &#xD;
The CT findings allowed a definitive diagnosis preoperatively in this case.</description>
    <dc:date>2009-12-30T15:00:00Z</dc:date>
  </item>
  <item rdf:about="http://hdl.handle.net/10564/1103">
    <title>腋窩に発生したhibernomaの一例</title>
    <link>http://hdl.handle.net/10564/1103</link>
    <description>タイトル: 腋窩に発生したhibernomaの一例
著者: 井上, 和也; 森田, 剛平; 城戸, 顕; 朴木, 寛弥; 笠井, 孝彦; 野々村, 昭孝
抄録: This is a case report of a hibernoma arising from the axilla. The patient, a &#xD;
54-year-old Japanese man, visited our hospital with the complaint of painless tumor in &#xD;
the left axilla. The size of the subcutaneous tumor was about 7 cm on palpation. On &#xD;
Magnetic Resonance Imaging (MRI), both T1-weighted and T2-weighted images of the &#xD;
tumor were homogenous high signal intensity, so we suspected lipoma. Subsequent MRI &#xD;
examination, however, revealed a non-fat part in the tumor. Because the tumor grew &#xD;
slowly, surgical therapy was performed to rule out malignancy. The resected tumor was &#xD;
14 × 11 × 6cm in size and exhibited a greasy, brown cut surface. Histopathological &#xD;
examination revealed multivacuolated brown fat cells with granular cytoplasm and small, &#xD;
central nuclei intermixed with ordinary white fat cells. Although brown fat cells &#xD;
somewhat resemble lipoblasts, nuclei of brown fat cells are small, non-atypical and &#xD;
centrally located, and are characteristically distributed evenly through the tumor &#xD;
unrelated to blood vessels. Vasculatures are relatively abundant. No mitosis and atypical &#xD;
cells were detected. On immunohistochemical examination, brown fat cells showed &#xD;
cytoplasmic expression of S-100, and no nuclear expression of MDM2. A diagnosis of &#xD;
hibernoma was made. Correct pathological diagnosis is important to avoid an erroneous &#xD;
diagnosis of well-differentiated liposarcoma because "Lipoma-like" subtypes morphologi- &#xD;
cally bear a striking resemblance to well-differentiated liposarcoma, but hibernoma is a &#xD;
benign tumor that does not recur with complete local excision. MDM2 immunostaining is &#xD;
a useful adjunct in diagnosing well-differentiated liposarcoma. The patient has survived &#xD;
for 3 months since the operation, and shows good QOL under the follow-up.</description>
    <dc:date>2009-12-30T15:00:00Z</dc:date>
  </item>
  <item rdf:about="http://hdl.handle.net/10564/1102">
    <title>Colonic adenocarcinomaに発生したcolonic moruleの一例</title>
    <link>http://hdl.handle.net/10564/1102</link>
    <description>タイトル: Colonic adenocarcinomaに発生したcolonic moruleの一例
著者: 殿村, 晴栄; 榎本, 泰典; 山岡, 健太郎; 武田, 麻衣子; 笠井, 孝彦; 野々村, 昭孝
抄録: We report a case of colonic morules with colonic adenocarcinoma. A &#xD;
69-year-old woman visited our hospital with the complaint of abdominal pain. The &#xD;
examination showed lower abdominal tenderness and muscular guarding. Ultrasonogra- &#xD;
phy and computed tomograpy showed inflanunatory change in the ileocecal region with &#xD;
cecal diverticula and presence of ascites. Surgical therapy was performed under a &#xD;
diagnosis of cecal perforation. The surgery revealed a cecal tumor which had ruptured. &#xD;
Iliocecal resection combined with lymph nodes dissection (D2) and peritoneal lavage was &#xD;
performed. Histopathological examination revealed that the cecal tumor showed well- &#xD;
differentiated adenocarcinoma with morular structures composed of small, oval cells with &#xD;
bland nuclei in a mulberry-like arrangement. On immunohistochemical examination, the &#xD;
morule showed nuclear overexpression of β catenin and CDX2, cytoplasmic &#xD;
overexpression of CD10, and no expression of cytokeratin 20. Correct pathological &#xD;
diagnosis is important to avoid an erroneous diagnosis of adenosquamous carcinoma &#xD;
because morules morphologically bear a striking resemblance to squamous metaplasia &#xD;
but are morphologically and qualitatively quite different from squamous metaplasia. She &#xD;
has survived for 1.5 years since the operation, and shows good QOL under the follow-up.</description>
    <dc:date>2009-12-30T15:00:00Z</dc:date>
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