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<title>OWL: OCOSH Classification/Bone Diseases/Orthopaedic Oncology/Connective and Soft Tissue Neoplasms/Bone Neoplasms/ Plasmacytoma</title>
<link>http://www.orthopaedicweblinks.com</link>
<description>Any discrete, presumably solitary, mass of neoplastic plasma cells either in bone marrow or various extramedullary sites.
OCOSH Code C04.557.386.720_BD_BN_PL</description>
<language>en-us</language>
<lastBuildDate>Tue Apr 15 2008 23:29:54 GMT</lastBuildDate>
<copyright>Copyright 2005 OWL Inc.</copyright>
<managingEditor>orthopaedicweblinks@gmail.com (Christian Veillette)</managingEditor>
<webMaster>orthopaedicweblinks@gmail.com (OWL Inc.)</webMaster>
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<title>Clinical Trials Plasmacytoma and Multiple Myeloma</title>
<link>http://www.orthopaedicweblinks.com/Detailed/10958.html</link>
<description>From database of clinical trials recuiting patients</description>
<pubDate>2007-03-28 23:29:54 GMT</pubDate>
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<author>Not Available</author>
</item><item>
<title>Extramedullary Plasmacytoma eMedicine</title>
<link>http://www.orthopaedicweblinks.com/Detailed/10956.html</link>
<description>A plasmacytoma is a discrete, solitary mass of neoplastic monoclonal plasma cells in either bone or soft tissue (extramedullary). Types are as follows:
Soft-tissue (extramedullary) plasmacytoma (SEP)
Solitary bone plasmacytoma (SBP)
Multifocal form of multiple myeloma
Multiple myeloma
Plasmablastic sarcoma
To simplify, solitary plasmacytomas can be divided into 2 groups according to location:
Plasmacytoma of the skeletal system (SBP)
Soft tissue (extramedullary) plasmacytoma (SEP)</description>
<pubDate>2007-03-28 23:29:54 GMT</pubDate>
<guid isPermaLink="false">http://www.orthopaedicweblinks.com/cgi-bin/owl/jump.cgi?ID=10956</guid>
<author>Fanning et al</author>
</item><item>
<title>Guidelines on the diagnosis and management of solitary plasmacytoma</title>
<link>http://www.orthopaedicweblinks.com/Detailed/10957.html</link>
<description>Guidelines on the diagnosis and management of solitary plasmacytoma of bone and solitary extramedullary plasmacytoma.
National Guideline Clearinghouse</description>
<pubDate>2007-03-28 23:29:54 GMT</pubDate>
<guid isPermaLink="false">http://www.orthopaedicweblinks.com/cgi-bin/owl/jump.cgi?ID=10957</guid>
<author>Not Available</author>
</item><item>
<title>Multiple Myeloma and Other Plasma Cell Neoplasms PDQ</title>
<link>http://www.orthopaedicweblinks.com/Detailed/11904.html</link>
<description>Multiple Myeloma and Other Plasma Cell Neoplasms (PDQ®): Treatment&lt;br&gt;
Multiple myeloma is a systemic malignancy of plasma cells that is highly treatable but rarely curable. It is potentially curable when it presents as a solitary plasmacytoma of bone or as an extramedullary plasmacytoma. The median survival in the prechemotherapy era was about 7 months. After the introduction of chemotherapy, prognosis improved significantly with a median survival of 24 to 30 months and a 10-year survival of 3%.</description>
<pubDate>2007-07-10 23:29:54 GMT</pubDate>
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<author>Not Available</author>
</item><item>
<title>Plasmacytoma doctors doctor</title>
<link>http://www.orthopaedicweblinks.com/Detailed/10959.html</link>
<description>The Doctor&#039;s Doctor
Plasmacytoma is a localized collection of monoclonal plasma cells. The disease is divided into primary plasmacytoma of the bone and extramedullary plasmacytoma. The importance of the diagnosis rests with the potential for these disorders to progress to multiple myeloma. Solitary plasmacytoma of the bone are usually painful and present with a lytic lesion on radiographs.</description>
<pubDate>2007-03-28 23:29:54 GMT</pubDate>
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<author>Not Available</author>
</item><item>
<title>Solitary Bone and Extramedullary Plasmacytoma</title>
<link>http://www.orthopaedicweblinks.com/Detailed/10960.html</link>
<description>Abstract
Less than 5% of patients with a plasma cell dyscrasia present with a single bone (SBP) or extramedullary plasmacytoma (EMP) without evidence of systemic disease (normocalcemia, absence of anemia, preservation of uninvolved immunoglobulins, or renal disease attributable to myeloma). Diagnosis requires biopsy confirmation of a monoclonal plasma cell infiltrate from a single site. The treatment of choice for both entities is radiotherapy given with curative intent (&gt; 4000 cGy) resulting in long term disease-free survival in approximately 30% of patients with SBP and 65% of patients with EMP
Full text available
Hematology 2005
© 2005 The American Society of Hematology </description>
<pubDate>2007-03-28 23:29:54 GMT</pubDate>
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<author>D M Weber</author>
</item><item>
<title>plasmacytoma</title>
<link>http://www.orthopaedicweblinks.com/Detailed/3352.html</link>
<description>Radiology case 4411-3451 </description>
<pubDate>2002-01-31 23:29:54 GMT</pubDate>
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<author></author>
</item><item>
<title>Plasmacytoma</title>
<link>http://www.orthopaedicweblinks.com/Detailed/3353.html</link>
<description>Radiology case 454-3451 </description>
<pubDate>2002-01-31 23:29:54 GMT</pubDate>
<guid isPermaLink="false">http://www.orthopaedicweblinks.com/cgi-bin/owl/jump.cgi?ID=3353</guid>
<author></author>
</item><item>
<title>Solitary myeloma (plasmacytoma)</title>
<link>http://www.orthopaedicweblinks.com/Detailed/6500.html</link>
<description>solitary plasmacytoma</description>
<pubDate>2002-02-04 23:29:54 GMT</pubDate>
<guid isPermaLink="false">http://www.orthopaedicweblinks.com/cgi-bin/owl/jump.cgi?ID=6500</guid>
<author></author>
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