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	<title>Mesothelioma Journal Articles &#187; Diffuse mesothelioma</title>
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	<description>Journal Articles on Mesothelioma: Cancer Information for Patients and Families</description>
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		<title>Diffuse malignant pleural mesothelioma: A multi-institutional clinicopathological study</title>
		<link>http://www.mesothelioma-line.com/articles/2008/10/31/diffuse-malignant-pleural-mesothelioma-a-multi-institutional-clinicopathological-study/</link>
		<comments>http://www.mesothelioma-line.com/articles/2008/10/31/diffuse-malignant-pleural-mesothelioma-a-multi-institutional-clinicopathological-study/#comments</comments>
		<pubDate>Fri, 31 Oct 2008 21:49:21 +0000</pubDate>
		<dc:creator>Administrator</dc:creator>
				<category><![CDATA[Diagnosis & Differentiation]]></category>
		<category><![CDATA[Diffuse mesothelioma]]></category>
		<category><![CDATA[Full Archive]]></category>
		<category><![CDATA[Pleural]]></category>
		<category><![CDATA[Surgery]]></category>
		<category><![CDATA[Survival]]></category>
		<category><![CDATA[Treatment]]></category>
		<category><![CDATA[Type of Mesothelioma:]]></category>

		<guid isPermaLink="false">http://www.mesothelioma-line.com/articles/?p=1486</guid>
		<description><![CDATA[Surgery Today. 2008;38(11):993-8. Epub 2008 Oct 29. [Link] Iyoda A, Yusa T, Kadoyama C, Sasaki K, Kimura H, Yamakawa H, Shiba M, Fujisawa T, Yoshino I. Department of Thoracic Surgery, Graduate School of Medicine, Chiba University, 1-8-1 Inohana, Chuo-ku, Chiba, 260-8670, Japan. Abstract Purpose: The relative rarity of malignant pleural mesothelioma (MPM) in Japan makes [...]]]></description>
			<content:encoded><![CDATA[<p><em>	Surgery Today</em>. 2008;38(11):993-8. Epub 2008 Oct 29. [<a href="http://www.springerlink.com/content/g53x15p6694mp526/" target="_blank">Link</a>]</p>
<p><strong>Iyoda A, Yusa T, Kadoyama C, Sasaki K, Kimura H, Yamakawa H, Shiba M, Fujisawa T, Yoshino I.</strong></p>
<p>Department of Thoracic Surgery, Graduate School of Medicine, Chiba University, 1-8-1 Inohana, Chuo-ku, Chiba, 260-8670, Japan.</p>
<h3 class="abstract">Abstract</h3>
<p><strong>Purpose</strong>: The relative rarity of malignant pleural mesothelioma (MPM) in Japan makes it difficult to perform a large-scale clinicopathological study of this tumor at a single institute. Thus, we performed a multiinstitutional study to evaluate the current status of diagnosis and treatment in Japan.</p>
<p><strong>Methods</strong>: We analyzed the records of 65 patients with MPM, obtained from the 13 institutions comprising the Japanese Chiba Multicenter Study Group.</p>
<p><strong>Results</strong>: In 56 patients, the tumor was detected after a visit to a medical facility for subjective symptoms such as chest pain, shortness of breath, and cough. It took a median period of 2 months from the initial visit to establish the diagnosis. The overall survival rates of 33 patients with unresectable MPM 1, 2, and 3 years after the diagnosis were 40.5%, 10.8%, and 0%, respectively, whereas those of 32 patients who underwent surgery were 67.9%, 35.0% and 10.9%, respectively (P = 0.0035). According to multivariate analysis, histological type, International Mesothelioma Interest Group clinical stage, sex, and the presenting symptom of shortness of breath were significant prognostic factors.</p>
<p><strong>Conclusions</strong>: The definitive diagnosis of early MPM is difficult, but establishing the best diagnostic modality would improve survival rates, since radical surgery is likely to be effective for resectable disease.</p>
<p><strong>Keywords</strong>: Diffuse malignant pleural mesothelioma &#8211; Hyaluronic acid &#8211; Thoracoscopic pleural biopsy &#8211; Pleuropneumonectomy </p>
<h3 class="glossary">Glossary</h3><dl class="glossary"><dt>diagnosis</dt><dd> identifying a disease by its signs or symptoms, and by using imaging procedures and laboratory findings. The earlier a diagnosis of cancer is made, the better the chance for long-term survival.</dd><dt>biopsy</dt><dd><span class="pronunciation">(buy-op-see)</span> the removal of a sample of tissue to see whether cancer cells are present. There are several kinds of biopsies. In some, a very thin needle is used to draw fluid and cells from a lump. In a core biopsy, a larger needle is used to remove more tissue.</dd><dt>tumor</dt><dd> an abnormal lump or mass of tissue. Tumors can be benign (not cancerous) or malignant (cancerous).</dd><dt>mesothelioma</dt><dd>a tumor derived from mesothelial tissue, such as the peritoneum (lining the abdomen) or pleura (lining the lungs). More on <a href="http://www.mesotheliomacenter.org/">mesothelioma</a>. </dd></dl>]]></content:encoded>
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		<title>Peritoneal Mesotheliomas: Clinicopathologic Features, CT Findings, and Differential Diagnosis</title>
		<link>http://www.mesothelioma-line.com/articles/2008/09/17/peritoneal-mesotheliomas-clinicopathologic-features-ct-findings-and-differential-diagnosis/</link>
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		<pubDate>Wed, 17 Sep 2008 22:23:15 +0000</pubDate>
		<dc:creator>Administrator</dc:creator>
				<category><![CDATA[CT or CAT scan]]></category>
		<category><![CDATA[Diagnosis & Differentiation]]></category>
		<category><![CDATA[Diffuse mesothelioma]]></category>
		<category><![CDATA[Full Archive]]></category>
		<category><![CDATA[Peritoneal (Abdominal Mesothelioma)]]></category>

		<guid isPermaLink="false">http://www.mesothelioma-line.com/articles/?p=1390</guid>
		<description><![CDATA[American Roentgen Ray Society. 2008 Sep;191(3):814-25. [Link] Park JY, Kim KW, Kwon HJ, Park MS, Kwon GY, Jun SY, Yu ES. Department of Radiology, Asan Medical Center, University of Ulsan College of Medicine, 388-1 Pungnap 2-dong, Songpa-ku, Seoul 138-736, South Korea. Abstract Objective: The objective of our study was to illustrate various CT findings of [...]]]></description>
			<content:encoded><![CDATA[<p><em>American Roentgen Ray Society</em>. 2008 Sep;191(3):814-25.  [<a href="http://www.ajronline.org/cgi/content/abstract/191/3/814" target="_blank">Link</a>]</p>
<p><strong>Park JY, Kim KW, Kwon HJ, Park MS, Kwon GY, Jun SY, Yu ES.</strong></p>
<p>Department of Radiology, Asan Medical Center, University of Ulsan College of Medicine, 388-1 Pungnap 2-dong, Songpa-ku, Seoul 138-736, South Korea.</p>
<h3 class="abstract">Abstract </h3>
<p><strong>Objective</strong>: The objective of our study was to illustrate various CT findings of peritoneal mesotheliomas, to review their clinicopathologic features, and to discuss the differential diagnoses.</p>
<p><strong>Conclusion</strong>: The clinicopathologic features of peritoneal mesotheliomas vary among the subtypes such as malignant mesotheliomas, cystic mesotheliomas, and well-differentiated papillary mesotheliomas, and accordingly, there is a spectrum of CT appearances. </p>
<p><strong>Keywords</strong>: CT, cystic mesothelioma, mesothelioma, oncologic imaging, papillary mesothelioma, peritoneum</p>
<h3 class="glossary">Glossary</h3><dl class="glossary"><dt>imaging</dt><dd> any method used to produce a picture of internal body structures. Some imaging methods used to detect cancer are x-rays (including mammograms and CT scans), magnetic resonance imaging (MRI), scintigraphy, and ultrasound.</dd><dt>mesothelioma</dt><dd>a tumor derived from mesothelial tissue, such as the peritoneum (lining the abdomen) or pleura (lining the lungs). More on <a href="http://www.mesotheliomacenter.org/">mesothelioma</a>. </dd><dt>peritoneal</dt><dd><span class="pronunciation">(pair-uh-tuh-nee-al)</span> the serous membrane that lines the cavity of the abdomen. (More on <a href="http://www.mesotheliomacenter.org/about/peritoneal-mesothelioma.php" target="_blank" title="(opens in a new window.)">Peritoneal Mesothelioma</a>.)  </dd></dl>]]></content:encoded>
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		<title>Metastatic appendiceal mucinous adenocarcinoma to well-differentiated diffuse mesothelioma of the peritoneal cavity: a mimicker of florid mesothelial hyperplasia in association with neoplasms</title>
		<link>http://www.mesothelioma-line.com/articles/2008/08/30/metastatic-appendiceal-mucinous-adenocarcinoma-to-well-differentiated-diffuse-mesothelioma-of-the-peritoneal-cavity-a-mimicker-of-florid-mesothelial-hyperplasia-in-association-with-neoplasms/</link>
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		<pubDate>Sat, 30 Aug 2008 17:11:42 +0000</pubDate>
		<dc:creator>Administrator</dc:creator>
				<category><![CDATA[Case Study]]></category>
		<category><![CDATA[Diagnosis & Differentiation]]></category>
		<category><![CDATA[Diffuse mesothelioma]]></category>
		<category><![CDATA[Full Archive]]></category>
		<category><![CDATA[Peritoneal (Abdominal Mesothelioma)]]></category>
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		<category><![CDATA[laparoscopy]]></category>

		<guid isPermaLink="false">http://www.mesothelioma-line.com/articles/?p=1330</guid>
		<description><![CDATA[International Journal of Gynecological Pathology. 2008 Oct;27(4):526-30. [Link] Tran TA, Holloway RW, Finkler NJ. Department of Pathology, Florida Hospital Orlando, Orlando, Florida 32803, USA. trannguyentienanh@hotmail.com Abstract Atypical/florid mesothelial hyperplasia associated with another neoplastic process is not an infrequent phenomenon and has been reported in a variety of tumors. In those instances, the mesothelial proliferation might [...]]]></description>
			<content:encoded><![CDATA[<p> <em>International Journal of Gynecological Pathology</em>. 2008 Oct;27(4):526-30. [<a href="http://www.ncbi.nlm.nih.gov/pubmed/18753969?dopt=AbstractPlus" target="_blank">Link]</a></p>
<p><a href="http://www.ncbi.nlm.nih.gov/pubmed/18753969?dopt=AbstractPlus"><strong> Tran TA, Holloway RW, Finkler NJ.</strong></a></p>
<p> Department of Pathology, Florida Hospital Orlando, Orlando, Florida 32803, USA. trannguyentienanh@hotmail.com</p>
<h3 class="abstract">Abstract</h3>
<p> Atypical/florid mesothelial hyperplasia associated with another neoplastic process is not an infrequent phenomenon and has been reported in a variety of tumors. In those instances, the mesothelial proliferation might create a misdiagnosis of metastatic carcinoma but seldom raises the possibility of a well-differentiated mesothelioma seeded by metastatic neoplastic cells. Herein, we report the case of a 40-year-old woman originally diagnosed with exuberant atypical mesothelial hyperplasia after an diagnostic laparoscopy. The subsequent operation, however, demonstrated a mucinous neoplasm of the appendix with involvement of the peritoneal cavity in the form of peritoneal mucinous carcinomatosis as well as metastases to the uterine serosa and adnexal surfaces. Microscopic analysis revealed an appendiceal adenocarcinoma with signet-ring-cell features that has metastasized to a diffuse well-differentiated mesothelioma of the peritoneal cavity. In many areas, the atypical mesothelial proliferation is indistinguishable from florid mesothelial hyperplasia. The true nature of the mesothelial proliferation was only confirmed after extensive additional sampling, which showed unequivocal stromal invasion. To the best of our knowledge, this is the first report of a metastatic appendiceal mucinous adenocarcinoma to a well-differentiated diffuse mesothelioma of the peritoneal cavity. Although commonly associated with atypical/ florid mesothelial hyperplasia, a carcinoma can rarely metastasize to a well-differentiated mesothelioma, which can pose significant diagnostic difficulties because it can mimic a reactive process. This unusual case report expands the spectrum of mesothelial proliferation in conjunction with a malignant neoplasm and serves to remind pathologists that such a concomitant occurrence exists.</p>
<h3 class="glossary">Glossary</h3><dl class="glossary"><dt>adenocarcinoma</dt><dd><span class="pronunciation">(add-en-o car-sin-o-muh)</span>. Cancer that starts in the glandular tissue, such as in the ducts or lobules of the breast.</dd><dt>neoplasm</dt><dd><span class="pronunciation">(nee-o-plas-um)</span> an abnormal growth (tumor) that starts from a single altered cell; a neoplasm may be benign or malignant. Cancer is a malignant neoplasm.</dd><dt>hyperplasia</dt><dd><span class="pronunciation">(hy-per-PLAY-zuh)</span> too much growth of cells or tissue in a specific area, such as the lining of the breast ducts or the prostate. By itself, hyperplasia is not cancerous, but when there is a lot of growth or the cells are not like normal cells, the risk of cancer developing is greater.</dd><dt>cell</dt><dd>the basic unit of which all living things are made. Cells replace themselves by splitting and forming new cells (mitosis). The processes that control the formation of new cells and the death of old cells are disrupted in cancer.</dd><dt>carcinoma</dt><dd><span class="pronunciation">(car-sin-o-ma)</span> a malignant tumor that begins in the lining layer (epithelial cells) of organs. At least 80% of all cancers are carcinomas.</dd><dt>atypical</dt><dd><span class="pronunciation">(A-tip-uh-kul)</span> not usual; abnormal. Often refers to the appearance of cancerous or precancerous cells. (See also <a href="/articles/glossary/?id=115">hyperplasia</a>.)</dd><dt>mesothelioma</dt><dd>a tumor derived from mesothelial tissue, such as the peritoneum (lining the abdomen) or pleura (lining the lungs). More on <a href="http://www.mesotheliomacenter.org/">mesothelioma</a>. </dd><dt>peritoneal</dt><dd><span class="pronunciation">(pair-uh-tuh-nee-al)</span> the serous membrane that lines the cavity of the abdomen. (More on <a href="http://www.mesotheliomacenter.org/about/peritoneal-mesothelioma.php" target="_blank" title="(opens in a new window.)">Peritoneal Mesothelioma</a>.)  </dd></dl>]]></content:encoded>
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		<title>Pulmonary sarcomatous tumors</title>
		<link>http://www.mesothelioma-line.com/articles/2008/07/09/pulmonary-sarcomatous-tumors/</link>
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		<pubDate>Wed, 09 Jul 2008 14:52:18 +0000</pubDate>
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				<category><![CDATA[Diagnosis & Differentiation]]></category>
		<category><![CDATA[Diffuse mesothelioma]]></category>
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		<category><![CDATA[Immunohistochemistry or IHC]]></category>
		<category><![CDATA[Type of Assessment:]]></category>
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		<guid isPermaLink="false">http://www.mesothelioma-line.com/articles/?p=1256</guid>
		<description><![CDATA[Archives of Pathology and Laboratory Medicine. 2008 Jul;132(7):1104-17. [Link] Litzky LA. Department of Pathology and Laboratory Medicine, University of Pennsylvania Medical Center, Philadelphia, PA 19104-4283, USA. lalitzky@mail.med.upenn.edu Abstract Context: Sarcomatous pulmonary neoplasms are a rare and diagnostically challenging group of tumors. Primary pulmonary sarcomas must be distinguished from the more frequent occurrence of sarcoma metastatic [...]]]></description>
			<content:encoded><![CDATA[<p>	<em>Archives of Pathology and Laboratory Medicine.</em> 2008 Jul;132(7):1104-17. [<a href="http://arpa.allenpress.com/arpaonline/?request=get-abstract&#038;issn=1543-2165&#038;volume=132&#038;page=1104" target="_blank">Link</a>]</p>
<p><strong>Litzky LA.</strong></p>
<p>Department of Pathology and Laboratory Medicine, University of Pennsylvania Medical Center, Philadelphia, PA 19104-4283, USA. lalitzky@mail.med.upenn.edu</p>
<h3 class="abstract">Abstract </h3>
<p><strong>Context</strong>: Sarcomatous pulmonary neoplasms are a rare and diagnostically challenging group of tumors. Primary pulmonary sarcomas must be distinguished from the more frequent occurrence of sarcoma metastatic to the lung, primary pulmonary sarcomatoid carcinoma, and diffuse malignant mesothelioma involving the lung. In current practice, the general availability of ancillary diagnostic techniques, such as immunohistochemistry and molecular analysis, can reliably classify many sarcomatoid lesions.</p>
<p><strong>Objective</strong>: To review the literature and report on additional primary material about the application of immunohistochemistry and molecular analysis in the differential diagnosis pulmonary sarcomatous neoplasms.</p>
<p><strong>Data Sources</strong>: Literature review of relevant articles indexed in PubMed (National Library of Medicine) between 1961 and 2007 and primary material from the author&#8217;s institution.</p>
<p><strong>Conclusions</strong>: This review discusses specific criteria for the diagnosis of primary lung sarcomas and offers a practical approach to excluding other sarcoma-like lesions involving the lung. The pathologist has an essential role in evaluating these tumors and will often be the first to suggest an unusual, alternative diagnosis, which may have significant implications for patient care, therapy, and prognosis.</p>
<h3 class="glossary">Glossary</h3><dl class="glossary"><dt>therapy</dt><dd> any of the measures taken to treat a disease. Unproven therapy is any therapy that has not been scientifically tested and approved. Use of an unproven therapy instead of standard (proven) therapy is called alternative therapy. Some alternative therapies have dangerous or even life-threatening side effects. For others, the main danger is that a patient may lose the opportunity to benefit from standard therapy. Complementary therapy, on the other hand, refers to therapies used in addition to standard therapy. Some complementary therapies may help relieve certain symptoms of cancer, relieve side effects of standard cancer therapy, or improve a patient's sense of well-being. The ACS recommends that patients considering use of any alternative or complementary therapy discuss this with their health care team.</dd><dt>sarcoma</dt><dd><span class="pronunciation">(sar-co-muh)</span> a malignant tumor growing from connective tissues, such as cartilage, fat, muscle, or bone.</dd><dt>prognosis</dt><dd><span class="pronunciation">(prog-no-sis)</span> a prediction of the course of disease; the outlook for the cure of the patient. For example, women with breast cancer that was detected early and who received prompt treatment have a good prognosis.</dd><dt>pathologist</dt><dd><span class="pronunciation">(path-all-eh-jist)</span> a doctor who specializes in diagnosis and classification of diseases by laboratory tests (such as examination of tissue and cells under a microscope). The pathologist determines whether a lump is benign or cancerous.</dd><dt>diagnosis</dt><dd> identifying a disease by its signs or symptoms, and by using imaging procedures and laboratory findings. The earlier a diagnosis of cancer is made, the better the chance for long-term survival.</dd><dt>carcinoma</dt><dd><span class="pronunciation">(car-sin-o-ma)</span> a malignant tumor that begins in the lining layer (epithelial cells) of organs. At least 80% of all cancers are carcinomas.</dd><dt>mesothelioma</dt><dd>a tumor derived from mesothelial tissue, such as the peritoneum (lining the abdomen) or pleura (lining the lungs). More on <a href="http://www.mesotheliomacenter.org/">mesothelioma</a>. </dd></dl>]]></content:encoded>
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		<title>Primary pleural neoplasia: entities other than diffuse malignant mesothelioma</title>
		<link>http://www.mesothelioma-line.com/articles/2008/07/09/primary-pleural-neoplasia-entities-other-than-diffuse-malignant-mesothelioma/</link>
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		<pubDate>Wed, 09 Jul 2008 14:47:40 +0000</pubDate>
		<dc:creator>Administrator</dc:creator>
				<category><![CDATA[Diagnosis & Differentiation]]></category>
		<category><![CDATA[Diffuse mesothelioma]]></category>
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		<guid isPermaLink="false">http://www.mesothelioma-line.com/articles/?p=1255</guid>
		<description><![CDATA[Archives of Pathology and Laboratory Medicine. Vol. 132, No. 7, pp. 1149–1170. [Link] Guinee DG, Allen TC. Department of Pathology, Virginia Mason Medical Center, Seattle, WA, USA. Abstract Context: Overwhelmingly, the most common neoplasm involving the pleura is metastatic carcinoma. In contrast, diffuse malignant mesothelioma occurs relatively rarely; however, it is nonetheless the most common [...]]]></description>
			<content:encoded><![CDATA[<p>	<em>Archives of Pathology and Laboratory Medicine. </em>Vol. 132, No. 7, pp. 1149–1170. [<a href="http://arpa.allenpress.com/arpaonline/?request=get-abstract&amp;issn=1543-2165&amp;volume=132&amp;page=1149" target="_blank">Link</a>]</p>
<p><strong>Guinee DG, Allen TC.</strong></p>
<p>Department of Pathology, Virginia Mason Medical Center, Seattle, WA, USA.</p>
<h3 class="abstract">Abstract </h3>
<p><strong>Context</strong>: Overwhelmingly, the most common neoplasm involving the pleura is metastatic carcinoma. In contrast, diffuse malignant mesothelioma occurs relatively rarely; however, it is nonetheless the most common neoplasm primary to the pleura. Metastatic carcinoma and diffuse malignant mesothelioma each have their own prognostic and therapeutic characteristics. Other primary pleural neoplasms occur uncommonly or rarely, with their own prognostic and therapeutic characteristics.</p>
<p><strong>Objective</strong>: To review primary pleural neoplasms other than diffuse malignant mesothelioma, to better ensure correct diagnosis and optimal assessment of prognosis and treatment.</p>
<p><strong>Data Sources</strong>: Literature review and primary material from the authors&#8217; institutions.</p>
<p><strong>Conclusions</strong>: A nonexhaustive group of uncommon to rare benign and malignant primary pleural neoplasms— other than diffuse malignant mesothelioma—are presented, of which one must be aware in order to maintain an appropriate index of suspicion to include them in the differential diagnosis of a pleural tumor.</p>
<h3 class="glossary">Glossary</h3><dl class="glossary"><dt>prognosis</dt><dd><span class="pronunciation">(prog-no-sis)</span> a prediction of the course of disease; the outlook for the cure of the patient. For example, women with breast cancer that was detected early and who received prompt treatment have a good prognosis.</dd><dt>pleura</dt><dd><span class="pronunciation">(pler-uh)</span> the membrane around the lungs and lining of the chest cavity. (<a href="http://www.mesotheliomacenter.org/about/pleural-mesothelioma.php" target="_blank" title="(opens in a new window.)">Pleural mesothelioma</a>.)  </dd><dt>neoplasm</dt><dd><span class="pronunciation">(nee-o-plas-um)</span> an abnormal growth (tumor) that starts from a single altered cell; a neoplasm may be benign or malignant. Cancer is a malignant neoplasm.</dd><dt>diagnosis</dt><dd> identifying a disease by its signs or symptoms, and by using imaging procedures and laboratory findings. The earlier a diagnosis of cancer is made, the better the chance for long-term survival.</dd><dt>carcinoma</dt><dd><span class="pronunciation">(car-sin-o-ma)</span> a malignant tumor that begins in the lining layer (epithelial cells) of organs. At least 80% of all cancers are carcinomas.</dd><dt>benign</dt><dd><span class="pronunciation">(be-nine)</span> not cancer; not malignant.</dd><dt>tumor</dt><dd> an abnormal lump or mass of tissue. Tumors can be benign (not cancerous) or malignant (cancerous).</dd><dt>mesothelioma</dt><dd>a tumor derived from mesothelial tissue, such as the peritoneum (lining the abdomen) or pleura (lining the lungs). More on <a href="http://www.mesotheliomacenter.org/">mesothelioma</a>. </dd></dl>]]></content:encoded>
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		<title>Multiple mechanisms of telomere maintenance exist and differentially affect clinical outcome in diffuse malignant peritoneal mesothelioma</title>
		<link>http://www.mesothelioma-line.com/articles/2008/07/03/multiple-mechanisms-of-telomere-maintenance-exist-and-differentially-affect-clinical-outcome-in-diffuse-malignant-peritoneal-mesothelioma/</link>
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		<pubDate>Thu, 03 Jul 2008 16:35:50 +0000</pubDate>
		<dc:creator>Administrator</dc:creator>
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		<category><![CDATA[Type of Mesothelioma:]]></category>

		<guid isPermaLink="false">http://www.mesothelioma-line.com/articles/?p=1250</guid>
		<description><![CDATA[Clinical Cancer Research. 2008 Jul 1;14(13):4134-40. [Link] Villa R, Daidone MG, Motta R, Venturini L, De Marco C, Vannelli A, Kusamura S, Baratti D, Deraco M, Costa A, Reddel RR, Zaffaroni N. Authors&#8217; Affiliations: Departments of Experimental Oncology and Surgery, Fondazione Istituto di Ricovero e Cura a Carattere Scientifico, Istituto Nazionale dei Tumori, Milan, Italy; [...]]]></description>
			<content:encoded><![CDATA[<p><em>Clinical Cancer Research</em>. 2008 Jul 1;14(13):4134-40. [<a href="http://clincancerres.aacrjournals.org/cgi/content/abstract/14/13/4134" target="_blank">Link</a>]</p>
<p><strong>Villa R, Daidone MG, Motta R, Venturini L, De Marco C, Vannelli A, Kusamura S, Baratti D, Deraco M, Costa A, Reddel RR, Zaffaroni N.</strong></p>
<p>Authors&#8217; Affiliations: Departments of Experimental Oncology and Surgery, Fondazione Istituto di Ricovero e Cura a Carattere Scientifico, Istituto Nazionale dei Tumori, Milan, Italy; and Children&#8217;s Medical Research Institute, Westmead, Sydney, Australia.</p>
<h3>Abstract </h3>
<p><strong>Purpose</strong>: This study aims to investigate the prevalence of the two known telomere maintenance mechanisms, telomerase activity (TA) and alternative lengthening of telomeres (ALT), and to assess their prognostic relevance in diffuse malignant peritoneal mesothelioma (DMPM).</p>
<p><strong>Experimental Design</strong>: In 44 DMPM specimens obtained from 38 patients, TA was determined using the telomeric repeat amplification protocol and ALT was detected by assaying ALT-associated promyelocytic leukemia nuclear bodies. The prognostic significance of telomere maintenance mechanisms was analyzed by Cox regression in the overall series and in a subset of 29 patients who underwent a uniform treatment regimen consisting of cytoreductive surgery and hyperthermic i.p. chemotherapy.</p>
<p><strong>Results</strong>: Telomere maintenance mechanisms were detectable in 86.4% of DMPM: ALT or TA alone was found in 18.2% or 63.6% of lesions, respectively, whereas two cases (4.6%) were ALT+/TA+. TA and ALT proved to be inversely associated (P = 0.002). In the overall series, TA was prognostic for 4-year relapse (TA+ versus TA–, hazard ratio, 3.30; 95% confidence interval, 1.23-8.86; P = 0.018) and cancer-related death (TA+ versus TA–, hazard ratio, 3.56; 95% confidence interval, 1.03-12.51; P = 0.045), whereas ALT failed to significantly affect clinical outcome. These results held true also in the subset of patients submitted to uniform treatment with cytoreductive surgery and hyperthermic i.p. chemotherapy.</p>
<p><strong>Conclusions</strong>: Our results indicate that both known telomere maintenance mechanisms, TA and ALT, are present in DMPM and differentially affect patient prognosis.</p>
<h3 class="glossary">Glossary</h3><dl class="glossary"><dt>regimen</dt><dd><span class="pronunciation">(rej-uh-men)</span> a strict, regulated plan (such as diet, exercise, or other activity) designed to reach certain goals. In cancer treatment, a plan to treat cancer.</dd><dt>relapse</dt><dd> reappearance of cancer after a disease-free period. See recurrence.</dd><dt>prognosis</dt><dd><span class="pronunciation">(prog-no-sis)</span> a prediction of the course of disease; the outlook for the cure of the patient. For example, women with breast cancer that was detected early and who received prompt treatment have a good prognosis.</dd><dt>protocol</dt><dd><span class="pronunciation">(pro-teh-call)</span> a formal outline or plan, such as a description of what treatments a patient will receive and exactly when each should be given.</dd><dt>prevalence</dt><dd> a measure of the proportion of persons in the population with a certain disease at a given time.</dd><dt>oncology</dt><dd><span class="pronunciation">(on-call-o-jee)</span> the branch of medicine concerned with the diagnosis and treatment of cancer.</dd><dt>leukemia</dt><dd><span class="pronunciation">(loo-key-me-uh) </span>cancer of the blood or blood-forming organs. People with leukemia often have a noticeable increase in white blood cells (leukocytes).</dd><dt>chemotherapy</dt><dd><span class="pronunciation">(key-mo-THER-uh-pee)</span> treatment with drugs to destroy cancer cells. Chemotherapy is often used with surgery or radiation to treat cancer when the cancer has spread, when it has come back (recurred), or when there is a strong chance that it could recur.</dd><dt>cancer</dt><dd>malignancy; a group of diseases typified by abnormal, generally out-of-control, cell growth.</dd><dt>mesothelioma</dt><dd>a tumor derived from mesothelial tissue, such as the peritoneum (lining the abdomen) or pleura (lining the lungs). More on <a href="http://www.mesotheliomacenter.org/">mesothelioma</a>. </dd><dt>peritoneal</dt><dd><span class="pronunciation">(pair-uh-tuh-nee-al)</span> the serous membrane that lines the cavity of the abdomen. (More on <a href="http://www.mesotheliomacenter.org/about/peritoneal-mesothelioma.php" target="_blank" title="(opens in a new window.)">Peritoneal Mesothelioma</a>.)  </dd></dl>]]></content:encoded>
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		<title>Cytomorphologic features of well-differentiated papillary mesothelioma in peritoneal effusion: A case report</title>
		<link>http://www.mesothelioma-line.com/articles/2008/06/06/cytomorphologic-features-of-well-differentiated-papillary-mesothelioma-in-peritoneal-effusion-a-case-report/</link>
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		<pubDate>Fri, 06 Jun 2008 15:40:51 +0000</pubDate>
		<dc:creator>Administrator</dc:creator>
				<category><![CDATA[Case Study]]></category>
		<category><![CDATA[Diagnosis & Differentiation]]></category>
		<category><![CDATA[Diffuse mesothelioma]]></category>
		<category><![CDATA[Full Archive]]></category>
		<category><![CDATA[Immunohistochemistry or IHC]]></category>
		<category><![CDATA[Peritoneal (Abdominal Mesothelioma)]]></category>
		<category><![CDATA[Symptoms & Symptom Management]]></category>
		<category><![CDATA[Type of Assessment:]]></category>
		<category><![CDATA[Type of Mesothelioma:]]></category>

		<guid isPermaLink="false">http://www.mesothelioma-line.com/articles/?p=1210</guid>
		<description><![CDATA[Diagnostic Cytopathology. 2008 Jun 4;36(7):512-515. [Epub ahead of print] [Link] Ikeda K, Suzuki T, Tate G, Mitsuya T. Department of Pathology, Showa University Fujigaoka Hospital, Fujigaoka, Yokohama, Japan. Abstract Well-differentiated papillary mesothelioma (WDPM), a distinct subtype of diffuse malignant mesothelioma, usually occurs in the peritoneum and is seen most commonly in women of reproductive age. [...]]]></description>
			<content:encoded><![CDATA[<p><em>Diagnostic Cytopathology. </em>2008 Jun 4;36(7):512-515. [Epub ahead of print] [<a href="http://www3.interscience.wiley.com/journal/119816138/abstract?CRETRY=1&#038;SRETRY=0" target="_blank">Link</a>]</p>
<p><strong>Ikeda K, Suzuki T, Tate G, Mitsuya T.</strong></p>
<p>Department of Pathology, Showa University Fujigaoka Hospital, Fujigaoka, Yokohama, Japan.</p>
<h3>Abstract </h3>
<p>Well-differentiated papillary mesothelioma (WDPM), a distinct subtype of diffuse malignant mesothelioma, usually occurs in the peritoneum and is seen most commonly in women of reproductive age. Histologic features of WDPM include papillary growth and stout fibrous cores surrounded by a single layer of tumor cells. We present the case of a 73-year-old woman without subjective symptoms who showed signs of peritoneal effusion during a routine examination and for whom cytologic examination of the ascitic fluid was performed. Many spherical clusters, with a smooth external surface composed of a single layer of uniform cuboidal cells, were observed. Within each cluster, a collagenous ball showed light green Papanicolaou staining. Immunohistochemistry of surgical specimens showed tumor cells positive for calretinin, D<sub>2</sub>-40, and HBME-1 staining. The histologic diagnosis was WDPM. The identification of a collagenous ball within these clusters is a useful cytologic finding for the diagnosis of WDPM. WDPM should be suspected when numerous collagenous balls are present by effusion cytology and isolated cells are not.</p>
<p><strong>Keywords</strong>: well-differentiated papillary mesothelioma, peritoneal effusion, cytology, immunohistochemistry</p>
<h3 class="glossary">Glossary</h3><dl class="glossary"><dt>diagnosis</dt><dd> identifying a disease by its signs or symptoms, and by using imaging procedures and laboratory findings. The earlier a diagnosis of cancer is made, the better the chance for long-term survival.</dd><dt>cytology</dt><dd><span class="pronunciation">(cy-tahl-uh-gee)</span> the branch of science that deals with the structure and function of cells.</dd><dt>tumor</dt><dd> an abnormal lump or mass of tissue. Tumors can be benign (not cancerous) or malignant (cancerous).</dd><dt>mesothelioma</dt><dd>a tumor derived from mesothelial tissue, such as the peritoneum (lining the abdomen) or pleura (lining the lungs). More on <a href="http://www.mesotheliomacenter.org/">mesothelioma</a>. </dd><dt>peritoneal</dt><dd><span class="pronunciation">(pair-uh-tuh-nee-al)</span> the serous membrane that lines the cavity of the abdomen. (More on <a href="http://www.mesotheliomacenter.org/about/peritoneal-mesothelioma.php" target="_blank" title="(opens in a new window.)">Peritoneal Mesothelioma</a>.)  </dd></dl>]]></content:encoded>
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		<title>Targeting tumor-associated macrophages in an orthotopic murine model of diffuse malignant mesothelioma</title>
		<link>http://www.mesothelioma-line.com/articles/2008/04/01/targeting-tumor-associated-macrophages-in-an-orthotopic-murine-model-of-diffuse-malignant-mesothelioma/</link>
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		<pubDate>Tue, 01 Apr 2008 15:41:25 +0000</pubDate>
		<dc:creator>Administrator</dc:creator>
				<category><![CDATA[Determining Efficacy]]></category>
		<category><![CDATA[Diffuse mesothelioma]]></category>
		<category><![CDATA[Full Archive]]></category>
		<category><![CDATA[New & Novel]]></category>
		<category><![CDATA[Treatment]]></category>
		<category><![CDATA[Type of Assessment:]]></category>
		<category><![CDATA[Type of Mesothelioma:]]></category>

		<guid isPermaLink="false">http://www.mesothelioma-line.com/articles/2008/04/01/targeting-tumor-associated-macrophages-in-an-orthotopic-murine-model-of-diffuse-malignant-mesothelioma/</guid>
		<description><![CDATA[Molecular Cancer Therapeutics. 2008 Apr;7(4):788-99. Epub 2008 Mar 28. [Link] Miselis NR, Wu ZJ, Van Rooijen N, Kane AB. Department of Pathology and Laboratory Medicine, Brown University, Box G-E531, Providence, RI 02912. Nathan_Miselis@brown.edu. Abstract Tumors are a mixture of neoplastic and host stromal cells, which establish a microenvironment that contributes to tumor progression. In this [...]]]></description>
			<content:encoded><![CDATA[<p><em>Molecular Cancer Therapeutics</em>. 2008 Apr;7(4):788-99. Epub 2008 Mar 28. [<a href="http://mct.aacrjournals.org/cgi/content/abstract/7/4/788" target="_blank">Link</a>]</p>
<p><strong>Miselis NR, Wu ZJ, Van Rooijen N, Kane AB.</strong></p>
<p>Department of Pathology and Laboratory Medicine, Brown University, Box G-E531, Providence, RI 02912. Nathan_Miselis@brown.edu.</p>
<h3 class="abstract">Abstract </h3>
<p>Tumors are a mixture of neoplastic and host stromal cells, which establish a microenvironment that contributes to tumor progression. In this study, the contribution of tumor-associated macrophages (TAMs) to tumor growth and metastasis was examined using an orthotopic, immunocompetent murine model of diffuse malignant peritoneal mesothelioma. The expression profile of cytokines and chemokines in solid tumors was consistent with a M2-polarized, TAM-mediated immunosuppressive microenvironment. TAMs were targeted using liposome-encapsulated clodronate (CLIP). Exposure of tumor spheroids to CM-DiI-labeled CLIP <em>in situ</em> confirms targeting of macrophages and not mesothelioma cells. Intraperitoneal (i.p.) delivery of CLIP produced apoptosis in tumor spheroids and solid tumors in contrast to delivery of liposome-encapsulated PBS or PBS. Mice received an i.p. injection of mesothelioma cells with CLIP delivered i.p. every 5 days. This treatment protocol produces a 4-fold reduction in the number of tumors, a 17-fold reduction in the relative tumor burden, and a 5-fold reduction in invasion and metastasis when compared with mice exposed to liposome-encapsulated PBS or PBS. Following transplantation of tumor spheroids and treatment with CLIP, mice showed a 4-fold reduction in the number of tumors and a 15-fold reduction in relative tumor burden. Mice bearing established tumors showed a 2-fold reduction in the number of tumors and relative tumor burden when exposed to half the previous dose of CLIP delivered by repeated i.p. injection. These reductions in tumor burden are statistically significant and identify TAMs as an important host-derived cell that contributes to growth, invasion, and metastasis in diffuse malignant peritoneal mesothelioma.</p>
<h3 class="glossary">Glossary</h3><dl class="glossary"><dt>protocol</dt><dd><span class="pronunciation">(pro-teh-call)</span> a formal outline or plan, such as a description of what treatments a patient will receive and exactly when each should be given.</dd><dt>metastasis</dt><dd><span class="pronunciation">(meh-tas-teh-sis)</span><!--StartFragment --> the spread of cancer cells to distant areas of the body by way of the lymph system or bloodstream. </dd><dt>in situ</dt><dd> in place; localized and confined to one area. A very early stage of cancer.</dd><dt>cell</dt><dd>the basic unit of which all living things are made. Cells replace themselves by splitting and forming new cells (mitosis). The processes that control the formation of new cells and the death of old cells are disrupted in cancer.</dd><dt>cancer</dt><dd>malignancy; a group of diseases typified by abnormal, generally out-of-control, cell growth.</dd><dt>tumor</dt><dd> an abnormal lump or mass of tissue. Tumors can be benign (not cancerous) or malignant (cancerous).</dd><dt>mesothelioma</dt><dd>a tumor derived from mesothelial tissue, such as the peritoneum (lining the abdomen) or pleura (lining the lungs). More on <a href="http://www.mesotheliomacenter.org/">mesothelioma</a>. </dd><dt>peritoneal</dt><dd><span class="pronunciation">(pair-uh-tuh-nee-al)</span> the serous membrane that lines the cavity of the abdomen. (More on <a href="http://www.mesotheliomacenter.org/about/peritoneal-mesothelioma.php" target="_blank" title="(opens in a new window.)">Peritoneal Mesothelioma</a>.)  </dd><dt>apoptosis</dt><dd>a type of cell death in which the cell basically commits suicide; scientists believe some types of cancer may originate from an interruption of this programmed cell death, allowing cells to grow out of control.</dd></dl>]]></content:encoded>
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		<title>From the archives of the AFIP: primary peritoneal tumors: imaging features with pathologic correlation</title>
		<link>http://www.mesothelioma-line.com/articles/2008/03/20/from-the-archives-of-the-afip-primary-peritoneal-tumors-imaging-features-with-pathologic-correlation/</link>
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		<pubDate>Thu, 20 Mar 2008 14:52:57 +0000</pubDate>
		<dc:creator>Administrator</dc:creator>
				<category><![CDATA[Diagnosis & Differentiation]]></category>
		<category><![CDATA[Diffuse mesothelioma]]></category>
		<category><![CDATA[Full Archive]]></category>
		<category><![CDATA[General]]></category>
		<category><![CDATA[Peritoneal (Abdominal Mesothelioma)]]></category>
		<category><![CDATA[Type of Assessment:]]></category>
		<category><![CDATA[Type of Mesothelioma:]]></category>

		<guid isPermaLink="false">http://www.mesothelioma-line.com/articles/2008/03/20/from-the-archives-of-the-afip-primary-peritoneal-tumors-imaging-features-with-pathologic-correlation/</guid>
		<description><![CDATA[RadioGraphics. 2008 Mar-Apr;28(2):583-607; quiz 621-2. [Link] Levy AD, Arnáiz J, Shaw JC, Sobin LH. Department of Radiology and Radiological Sciences, Uniformed Services University of the Health Sciences, 4301 Jones Bridge Rd, Bethesda, MD 20814-4799, USA. alevy@usuhs.mil Abstract Primary peritoneal tumors are uncommon lesions that arise from the mesothelial or submesothelial layers of the peritoneum. Primary [...]]]></description>
			<content:encoded><![CDATA[<p><em>RadioGraphics</em>. 2008 Mar-Apr;28(2):583-607; quiz 621-2. [<a href="http://radiographics.rsnajnls.org/cgi/content/abstract/28/2/583" target="_blank">Link</a>]</p>
<p><strong>Levy AD, Arnáiz J, Shaw JC, Sobin LH.</strong></p>
<p> Department of Radiology and Radiological Sciences, Uniformed Services University of the Health Sciences, 4301 Jones Bridge Rd, Bethesda, MD 20814-4799, USA. alevy@usuhs.mil</p>
<h3>Abstract</h3>
<p> Primary peritoneal tumors are uncommon lesions that arise from the mesothelial or submesothelial layers of the peritoneum. Primary malignant mesothelioma, multicystic mesothelioma, primary peritoneal serous carcinoma, leiomyomatosis peritonealis disseminata, and desmoplastic small round cell tumor are the most prominent of these rare lesions. Primary malignant mesothelioma is a highly aggressive malignancy that occurs most commonly in older men and that has a strong association with high levels of asbestos exposure. It manifests most often as diffuse sheetlike or nodular thickening of the peritoneal surfaces, but it may occasionally be a localized mass. Multicystic mesothelioma occurs most frequently in women and has benign or indolent biologic behavior in the majority of patients. It is a multilocular cystic mass that arises from the pelvic peritoneal surfaces. Primary peritoneal serous carcinoma occurs almost exclusively in women. It is histologically identical to ovarian serous carcinoma and may be indistinguishable from metastatic ovarian carcinoma at imaging studies. Leiomyomatosis peritonealis disseminata is a rare, benign proliferative process that also occurs exclusively in women and is characterized by multiple smooth muscle nodules throughout the peritoneum. Desmoplastic small round cell tumor is a highly aggressive malignancy of unknown origin that occurs most often in the peritoneal cavity of young men. This unusual group of tumors is linked together by a common site of origin and imaging manifestations that mimic those of peritoneal carcinomatosis. Knowledge of the spectrum of imaging findings in this group of primary peritoneal tumors, along with their clinical and pathologic characteristics, is important in the evaluation of patients with diffuse peritoneal disease.</p>
<h3 class="glossary">Glossary</h3><dl class="glossary"><dt>imaging</dt><dd> any method used to produce a picture of internal body structures. Some imaging methods used to detect cancer are x-rays (including mammograms and CT scans), magnetic resonance imaging (MRI), scintigraphy, and ultrasound.</dd><dt>cell</dt><dd>the basic unit of which all living things are made. Cells replace themselves by splitting and forming new cells (mitosis). The processes that control the formation of new cells and the death of old cells are disrupted in cancer.</dd><dt>carcinoma</dt><dd><span class="pronunciation">(car-sin-o-ma)</span> a malignant tumor that begins in the lining layer (epithelial cells) of organs. At least 80% of all cancers are carcinomas.</dd><dt>benign</dt><dd><span class="pronunciation">(be-nine)</span> not cancer; not malignant.</dd><dt>tumor</dt><dd> an abnormal lump or mass of tissue. Tumors can be benign (not cancerous) or malignant (cancerous).</dd><dt>mesothelioma</dt><dd>a tumor derived from mesothelial tissue, such as the peritoneum (lining the abdomen) or pleura (lining the lungs). More on <a href="http://www.mesotheliomacenter.org/">mesothelioma</a>. </dd><dt>peritoneal</dt><dd><span class="pronunciation">(pair-uh-tuh-nee-al)</span> the serous membrane that lines the cavity of the abdomen. (More on <a href="http://www.mesotheliomacenter.org/about/peritoneal-mesothelioma.php" target="_blank" title="(opens in a new window.)">Peritoneal Mesothelioma</a>.)  </dd></dl>]]></content:encoded>
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		<title>Cytologic malignancy versus benignancy: how useful are the &#8220;newer&#8221; markers in body fluid cytology?</title>
		<link>http://www.mesothelioma-line.com/articles/2008/01/11/cytologic-malignancy-versus-benignancy-how-useful-are-the-newer-markers-in-body-fluid-cytology/</link>
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		<pubDate>Fri, 11 Jan 2008 19:55:31 +0000</pubDate>
		<dc:creator>Administrator</dc:creator>
				<category><![CDATA[Diagnosis & Differentiation]]></category>
		<category><![CDATA[Diffuse mesothelioma]]></category>
		<category><![CDATA[Full Archive]]></category>
		<category><![CDATA[Immunohistochemistry or IHC]]></category>
		<category><![CDATA[Pleural]]></category>
		<category><![CDATA[Type of Assessment:]]></category>
		<category><![CDATA[Type of Mesothelioma:]]></category>

		<guid isPermaLink="false">http://www.mesothelioma-line.com/articles/2008/01/11/cytologic-malignancy-versus-benignancy-how-useful-are-the-newer-markers-in-body-fluid-cytology/</guid>
		<description><![CDATA[Archives of Pathology and Laboratory Medicine. 2008 Jan;132(1):23-8. [Link] Lyons-Boudreaux V, Mody DR, Zhai J, Coffey D. Weill Medical College of Cornell University, The Methodist Hospital, Department of Pathology, Houston, TX 77030, USA. Abstract Context: Differentiating reactive effusion, malignant mesothelioma, and metastatic adenocarcinoma in body cavity fluids can be challenging. Interpreting immunohistochemical markers in cell [...]]]></description>
			<content:encoded><![CDATA[<p><em>Archives of Pathology and Laboratory Medicine</em>. 2008 Jan;132(1):23-8. [<a href="http://arpa.allenpress.com/arpaonline/?request=get-abstract&#038;issn=1543-2165&#038;volume=132&#038;page=23">Link</a>]</p>
<p><strong>Lyons-Boudreaux V, Mody DR, Zhai J, Coffey D.</strong></p>
<p>Weill Medical College of Cornell University, The Methodist Hospital, Department of Pathology, Houston, TX 77030, USA.</p>
<h3 class="abstract">Abstract</h3>
<p><strong>Context:</strong> Differentiating reactive effusion, malignant mesothelioma, and metastatic adenocarcinoma in body cavity fluids can  be challenging. Interpreting immunohistochemical markers in cell block  preparations can be difficult because of nonspecific staining, focal  staining, or poor staining quality. We selected a panel of conventional  and newer markers to assess their utility in evaluating effusions.</p>
<p><strong>Objective:</strong> To  evaluate the efficacy of 5 immunohistochemical markers in the  differential diagnosis of reactive mesothelial proliferation, malignant  mesothelioma, and metastatic adenocarcinoma in body cavity fluids.</p>
<p><strong>Design:</strong> A  total of 72 formalin-fixed, paraffin-embedded cell block specimens from  pleural and peritoneal effusions, including 5 mesotheliomas, 48  adenocarcinomas, and 19 benign effusions were stained with antibodies  against calretinin, D2-40, XIAP, MOC-31, and WT1.</p>
<p><strong>Results:</strong> All  benign effusions and mesotheliomas demonstrated diffuse membranous  staining with D2-40. All mesotheliomas displayed calretinin positivity,  whereas only 58% of benign effusions stained focally with calretinin.  MOC-31 was positive in all cases of adenocarcinoma, whereas all benign  effusions and mesotheliomas were negative. All cases of the metastatic  adenocarcinoma were negative for calretinin and D2-40. However,  background reactive mesothelial cells were positive for calretinin and  D2-40. Overall, D2-40 highlighted more mesothelial cells than  calretinin. WT1 was positive in 50% of benign effusions, 60% of  mesotheliomas, and 27% of adenocarcinomas. XIAP stained most  mesotheliomas (80%), some adenocarcinomas (51%), and rare benign  effusions (11%).</p>
<p><strong>Conclusions:</strong> MOC-31  and D2-40 were very sensitive and specific markers of epithelial and  mesothelial cells, respectively. Compared with calretinin, D2-40 was a  more sensitive marker of mesothelial cells. WT1 proved to be  nonspecific. XIAP was not a sensitive marker for malignancy and had a  limited value in cytology. We recommend using a panel to include MOC-31  and D2-40 to improve diagnostic accuracy in body cavity effusions.</p>
<h3 class="glossary">Glossary</h3><dl class="glossary"><dt>adenocarcinoma</dt><dd><span class="pronunciation">(add-en-o car-sin-o-muh)</span>. Cancer that starts in the glandular tissue, such as in the ducts or lobules of the breast.</dd><dt>diagnosis</dt><dd> identifying a disease by its signs or symptoms, and by using imaging procedures and laboratory findings. The earlier a diagnosis of cancer is made, the better the chance for long-term survival.</dd><dt>cytology</dt><dd><span class="pronunciation">(cy-tahl-uh-gee)</span> the branch of science that deals with the structure and function of cells.</dd><dt>cell</dt><dd>the basic unit of which all living things are made. Cells replace themselves by splitting and forming new cells (mitosis). The processes that control the formation of new cells and the death of old cells are disrupted in cancer.</dd><dt>benign</dt><dd><span class="pronunciation">(be-nine)</span> not cancer; not malignant.</dd><dt>mesothelioma</dt><dd>a tumor derived from mesothelial tissue, such as the peritoneum (lining the abdomen) or pleura (lining the lungs). More on <a href="http://www.mesotheliomacenter.org/">mesothelioma</a>. </dd><dt>peritoneal</dt><dd><span class="pronunciation">(pair-uh-tuh-nee-al)</span> the serous membrane that lines the cavity of the abdomen. (More on <a href="http://www.mesotheliomacenter.org/about/peritoneal-mesothelioma.php" target="_blank" title="(opens in a new window.)">Peritoneal Mesothelioma</a>.)  </dd></dl>]]></content:encoded>
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