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<title>Journal of Clinical Pathology</title>
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<title><![CDATA[Chronic gastric ulceration: a novel manifestation of IgG4-related disease?]]></title>
<link>http://jcp.bmj.com/cgi/content/short/65/6/569?rss=1</link>
<description><![CDATA[ <sec><st>Case report</st> <p>A 73-year-old woman who presented with anaemia and gastroscopy revealed a 30&nbsp;mm firm ulcer with raised edges at the lesser curve of the stomach. A CT scan revealed features within the ulcer that were suspicious for malignancy. She was treated with a proton pump inhibitor and sucralfate but the ulcer failed to heal over a 1-year period. Three sets of biopsies from the ulcer edge during this time revealed benign changes only. There was no history of non-steroidal anti-inflammatory drug usage and urinary salicylate estimation was negative. The serum gastrin concentration was not raised. Her medical history included insulin-dependent diabetes mellitus and ischaemic heart disease. There was no history of a systemic inflammatory disorder. Due to the continued concern of occult malignancy she proceeded to laparotomy with partial gastrectomy, after which she made an uneventful recovery.</p> <p>Macroscopic examination of the resection specimen revealed a 30&nbsp;mm mucosal ulcer...]]></description>
<dc:creator><![CDATA[Bateman, A. C., Sommerlad, M., Underwood, T. J.]]></dc:creator>
<dc:date>2012-05-19T05:47:01-07:00</dc:date>
<dc:identifier>info:doi/10.1136/jclinpath-2011-200565</dc:identifier>
<dc:identifier>hwp:master-id:jclinpath;jclinpath-2011-200565</dc:identifier>
<dc:publisher>BMJ Publishing Group</dc:publisher>
<dc:title><![CDATA[Chronic gastric ulceration: a novel manifestation of IgG4-related disease?]]></dc:title>
<prism:publicationDate>2012-06-01</prism:publicationDate>
<prism:section>PostScript</prism:section>
<prism:volume>65</prism:volume>
<prism:number>6</prism:number>
<prism:startingPage>569</prism:startingPage>
<prism:endingPage>570</prism:endingPage>
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<title><![CDATA[Epstein-Barr virus-associated intrahepatic cholangiocarcinoma bearing an intense lymphoplasmacytic infiltration]]></title>
<link>http://jcp.bmj.com/cgi/content/short/65/6/570?rss=1</link>
<description><![CDATA[ <sec><st>Introduction</st> <p>Lymphoepithelioma-like carcinoma (LELC) of the liver is extremely rare. To our knowledge, only 16 cases of pure LELC or LELC with ordinary adenocarcinoma arising in the hepatobiliary tract have been reported in the English literature.<cross-ref type="bib" refid="b1">1&ndash;7</cross-ref><cross-ref type="bib" refid="b2"></cross-ref><cross-ref type="bib" refid="b3"></cross-ref><cross-ref type="bib" refid="b4"></cross-ref><cross-ref type="bib" refid="b5"></cross-ref><cross-ref type="bib" refid="b6"></cross-ref><cross-ref type="bib" refid="b7"></cross-ref> Most of these tumours (68%, 11/16) were positive for Epstein&ndash;Barr virus (EBV) by EBV-encoded small non-polyadenylated RNA (EBER-1) in situ hybridisation.<cross-ref type="bib" refid="b1">1&ndash;6</cross-ref><cross-ref type="bib" refid="b2"></cross-ref><cross-ref type="bib" refid="b3"></cross-ref><cross-ref type="bib" refid="b4"></cross-ref><cross-ref type="bib" refid="b5"></cross-ref><cross-ref type="bib" refid="b6"></cross-ref> However, association of intrahepatic cholangiocarcinoma bearing an intense lymphoplasmacytic infiltration with EBV infection has not been reported. We were the first to present two cases of intrahepatic cholangiocarcinoma with dense lymphoplasmacytic infiltration from Southern China, an area that is well known for and has a high-incidence of nasopharyngeal carcinoma, showing EBV infection, but one case of LELC was associated with EBV infection as well.</p> </sec> <sec><st>Case...]]></description>
<dc:creator><![CDATA[Xiao, P., Shi, H., Zhang, H., Meng, F., Peng, J., Ke, Z., Wang, K., Liu, Y., Han, A.]]></dc:creator>
<dc:date>2012-05-19T05:47:01-07:00</dc:date>
<dc:identifier>info:doi/10.1136/jclinpath-2011-200581</dc:identifier>
<dc:identifier>hwp:master-id:jclinpath;jclinpath-2011-200581</dc:identifier>
<dc:publisher>BMJ Publishing Group</dc:publisher>
<dc:title><![CDATA[Epstein-Barr virus-associated intrahepatic cholangiocarcinoma bearing an intense lymphoplasmacytic infiltration]]></dc:title>
<prism:publicationDate>2012-06-01</prism:publicationDate>
<prism:section>PostScript</prism:section>
<prism:volume>65</prism:volume>
<prism:number>6</prism:number>
<prism:startingPage>570</prism:startingPage>
<prism:endingPage>573</prism:endingPage>
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<title><![CDATA[Ectopic prostatic tissue in the uterine cervix. Report of a case and brief overview of basaloid cervical glandular lesions]]></title>
<link>http://jcp.bmj.com/cgi/content/short/65/6/573?rss=1</link>
<description><![CDATA[ <sec><st>Case history</st> <p>A 31-year-old woman (gravida 0, para 0) was noted to have high-grade squamous intraepithelial lesion at routine two-yearly cervical smear. At colposcopy, three separate acetowhite areas were seen. The colposcopic impression was of low-grade squamous intraepithelial lesion and chronic inflammatory change. A Lletz biopsy of the cervix was performed. The patient had been on microgynon 50, which she had ceased before the last period. The last menstrual period was 3&nbsp;weeks prior to the colposcopy. No significant gynaecological or medical history was noted.</p> </sec> <sec><st>Pathological findings</st> <p>The gross specimen consisted of an intact Lletz biopsy of cervix measuring 17<FONT FACE="arial,helvetica">x</FONT>10&nbsp;mm and resected to a depth of 15&nbsp;mm. The tissue was transected and blocked in toto. Histologically, high-grade squamous intraepithelial lesion (CIN 2) and associated koilocytosis consistent with human papillomavirus was seen. Background changes of moderate chronic cervicitis and associated squamous metaplasia were present. An additional finding noted were three...]]></description>
<dc:creator><![CDATA[Singh, M.]]></dc:creator>
<dc:date>2012-05-19T05:47:01-07:00</dc:date>
<dc:identifier>info:doi/10.1136/jclinpath-2011-200455</dc:identifier>
<dc:identifier>hwp:master-id:jclinpath;jclinpath-2011-200455</dc:identifier>
<dc:publisher>BMJ Publishing Group</dc:publisher>
<dc:title><![CDATA[Ectopic prostatic tissue in the uterine cervix. Report of a case and brief overview of basaloid cervical glandular lesions]]></dc:title>
<prism:publicationDate>2012-06-01</prism:publicationDate>
<prism:section>PostScript</prism:section>
<prism:volume>65</prism:volume>
<prism:number>6</prism:number>
<prism:startingPage>573</prism:startingPage>
<prism:endingPage>575</prism:endingPage>
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<title><![CDATA[An unusual cause of ischaemic colitis]]></title>
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<description><![CDATA[ <p>Ischaemic colitis is commonly encountered in elderly patients and the underlying vascular insufficiency may be due to non-occlusive causes such as hypotension and occlusive aetiologies such as mesenteric artery thrombosis or embolism. We report an unusual case of ischaemic colitis due to an angiodestructive peripheral T cell lymphoma.</p> <p>A patient with hypertension, ischaemic heart disease, atrial fibrillation and recurrent strokes was admitted for acutely worsening abdominal distension and breathlessness. There was a history of persistent abdominal distension and diarrhoea, which were treated conservatively. Endoscopy done had shown reflux oesophagitis, peptic ulceration and right-sided ischaemic colitis. Per-rectal examination revealed blood clots mixed with mucus. CT of the abdomen and pelvis showed no evidence of mesenteric vascular occlusion or masses.</p> <p>The patient subsequently became hypotensive and underwent emergency laparotomy. Intraoperatively, ischaemic changes of left colon and patchy oedema of the mesentery were noted. Left hemicolectomy with colostomy was performed. Postoperatively, the...]]></description>
<dc:creator><![CDATA[Tan, S. Y., Looi, L. M., Teo, W. L., Yeoh, W. P., Chan, K. S.]]></dc:creator>
<dc:date>2012-05-19T05:47:01-07:00</dc:date>
<dc:identifier>info:doi/10.1136/jclinpath-2011-200618</dc:identifier>
<dc:identifier>hwp:master-id:jclinpath;jclinpath-2011-200618</dc:identifier>
<dc:publisher>BMJ Publishing Group</dc:publisher>
<dc:title><![CDATA[An unusual cause of ischaemic colitis]]></dc:title>
<prism:publicationDate>2012-06-01</prism:publicationDate>
<prism:section>PostScript</prism:section>
<prism:volume>65</prism:volume>
<prism:number>6</prism:number>
<prism:startingPage>575</prism:startingPage>
<prism:endingPage>576</prism:endingPage>
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