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Paraganglioma of the duodenum in association with congenital neurofibromatosis possible relationship
A case of a duodenal paraganglioma in a patient with von Recklinghausen's disease is presented, along with a review of the common clinical features of the 26 cases of duodenal paraganglioma and related neurogenic tumors reported in the literature. There was no reported evidence of recurrence or...
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| Published in: | Cancer 1984-06, Vol.53 (11), p.2491-2496 |
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| Main Authors: | , |
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| Language: | English |
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| container_end_page | 2496 |
| container_issue | 11 |
| container_start_page | 2491 |
| container_title | Cancer |
| container_volume | 53 |
| creator | Kheir, Sonia M. Halpern, Norman B. |
| description | A case of a duodenal paraganglioma in a patient with von Recklinghausen's disease is presented, along with a review of the common clinical features of the 26 cases of duodenal paraganglioma and related neurogenic tumors reported in the literature. There was no reported evidence of recurrence or metastasis. Local excision was the most commonly employed method of treatment. It is proposed that duodenal paraganglioma with its admixed components and variable histologic features may represent hamartomatous hyperplasia of the paraganglia and the supporting neuroid tissue in this area. This would explain the benign behavior of these tumors as compared with carcinoids. Its association, in this case, with neurofibromatosis supports the neural crest origin of duodenal paragangliomas. |
| doi_str_mv | 10.1002/1097-0142(19840601)53:11<2491::AID-CNCR2820531122>3.0.CO;2-S |
| format | article |
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There was no reported evidence of recurrence or metastasis. Local excision was the most commonly employed method of treatment. It is proposed that duodenal paraganglioma with its admixed components and variable histologic features may represent hamartomatous hyperplasia of the paraganglia and the supporting neuroid tissue in this area. This would explain the benign behavior of these tumors as compared with carcinoids. Its association, in this case, with neurofibromatosis supports the neural crest origin of duodenal paragangliomas.</description><identifier>ISSN: 0008-543X</identifier><identifier>EISSN: 1097-0142</identifier><identifier>DOI: 10.1002/1097-0142(19840601)53:11<2491::AID-CNCR2820531122>3.0.CO;2-S</identifier><identifier>PMID: 6201261</identifier><identifier>CODEN: CANCAR</identifier><language>eng</language><publisher>New York: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>Biological and medical sciences ; Cytoplasmic Granules - ultrastructure ; Duodenal Neoplasms - pathology ; Duodenal Neoplasms - ultrastructure ; Female ; Gastroenterology. Liver. Pancreas. Abdomen ; Humans ; Male ; Medical sciences ; Microscopy, Electron ; Middle Aged ; Neoplasms, Multiple Primary ; Neurofibromatosis 1 - congenital ; Neurofibromatosis 1 - pathology ; Paraganglioma - pathology ; Paraganglioma - ultrastructure ; Sex Factors ; Skin Neoplasms - congenital ; Skin Neoplasms - pathology ; Staining and Labeling ; Stomach. Duodenum. Small intestine. Colon. Rectum. Anus ; Tumors</subject><ispartof>Cancer, 1984-06, Vol.53 (11), p.2491-2496</ispartof><rights>Copyright © 1984 American Cancer Society</rights><rights>1985 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c5012-65beee8f96a3824bb088e12ec958d361d0de3ee6dff2254bd7fc011b43c9d0a83</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=8867525$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/6201261$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kheir, Sonia M.</creatorcontrib><creatorcontrib>Halpern, Norman B.</creatorcontrib><title>Paraganglioma of the duodenum in association with congenital neurofibromatosis possible relationship</title><title>Cancer</title><addtitle>Cancer</addtitle><description>A case of a duodenal paraganglioma in a patient with von Recklinghausen's disease is presented, along with a review of the common clinical features of the 26 cases of duodenal paraganglioma and related neurogenic tumors reported in the literature. There was no reported evidence of recurrence or metastasis. Local excision was the most commonly employed method of treatment. It is proposed that duodenal paraganglioma with its admixed components and variable histologic features may represent hamartomatous hyperplasia of the paraganglia and the supporting neuroid tissue in this area. This would explain the benign behavior of these tumors as compared with carcinoids. Its association, in this case, with neurofibromatosis supports the neural crest origin of duodenal paragangliomas.</description><subject>Biological and medical sciences</subject><subject>Cytoplasmic Granules - ultrastructure</subject><subject>Duodenal Neoplasms - pathology</subject><subject>Duodenal Neoplasms - ultrastructure</subject><subject>Female</subject><subject>Gastroenterology. Liver. Pancreas. Abdomen</subject><subject>Humans</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Microscopy, Electron</subject><subject>Middle Aged</subject><subject>Neoplasms, Multiple Primary</subject><subject>Neurofibromatosis 1 - congenital</subject><subject>Neurofibromatosis 1 - pathology</subject><subject>Paraganglioma - pathology</subject><subject>Paraganglioma - ultrastructure</subject><subject>Sex Factors</subject><subject>Skin Neoplasms - congenital</subject><subject>Skin Neoplasms - pathology</subject><subject>Staining and Labeling</subject><subject>Stomach. Duodenum. Small intestine. Colon. Rectum. Anus</subject><subject>Tumors</subject><issn>0008-543X</issn><issn>1097-0142</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1984</creationdate><recordtype>article</recordtype><recordid>eNqVkV-L1DAUxYMo6zj6EYQ8iOhDx9yk6aSjCEvXPwuLI66CD0JIk9uZSNuMScuy396OMw7og-BTCPecw-H8CLkAtgDG-Atg5TJjkPNnUKqcFQyeS7ECeMXzElar88uLrPpQfeKKMykAOH8tFmxRrV_y7PoOmZ3sd8mMMaYymYuv98mDlL5P3yWX4oycFZwBL2BG3EcTzcb0m9aHztDQ0GGL1I3BYT921PfUpBSsN4MPPb3xw5ba0G-w94NpaY9jDI2v4-QdQvKJ7kJKvm6RRmx_edLW7x6Se41pEz46vnPy5e2bz9X77Gr97rI6v8qsnOpkhawRUTVlYYTieV0zpRA42lIqJwpwzKFALFzTcC7z2i0bywDqXNjSMaPEnDw95O5i-DFiGnTnk8W2NT2GMWkFjMtiWU7CbwehjVPfiI3eRd-ZeKuB6T0EvV9R71fUvyFoKTSA3kPQeoKg_4SghWa6Wmuur6f4x8ceY92hO4UfV5_uT453k6xpm2h669NJplSxlBOnOdkcZDe-xdv_rPjPhn9dxE_z_bQE</recordid><startdate>19840601</startdate><enddate>19840601</enddate><creator>Kheir, Sonia M.</creator><creator>Halpern, Norman B.</creator><general>Wiley Subscription Services, Inc., A Wiley Company</general><general>Wiley-Liss</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>19840601</creationdate><title>Paraganglioma of the duodenum in association with congenital neurofibromatosis possible relationship</title><author>Kheir, Sonia M. ; Halpern, Norman B.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5012-65beee8f96a3824bb088e12ec958d361d0de3ee6dff2254bd7fc011b43c9d0a83</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1984</creationdate><topic>Biological and medical sciences</topic><topic>Cytoplasmic Granules - ultrastructure</topic><topic>Duodenal Neoplasms - pathology</topic><topic>Duodenal Neoplasms - ultrastructure</topic><topic>Female</topic><topic>Gastroenterology. Liver. Pancreas. Abdomen</topic><topic>Humans</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Microscopy, Electron</topic><topic>Middle Aged</topic><topic>Neoplasms, Multiple Primary</topic><topic>Neurofibromatosis 1 - congenital</topic><topic>Neurofibromatosis 1 - pathology</topic><topic>Paraganglioma - pathology</topic><topic>Paraganglioma - ultrastructure</topic><topic>Sex Factors</topic><topic>Skin Neoplasms - congenital</topic><topic>Skin Neoplasms - pathology</topic><topic>Staining and Labeling</topic><topic>Stomach. Duodenum. Small intestine. Colon. Rectum. Anus</topic><topic>Tumors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kheir, Sonia M.</creatorcontrib><creatorcontrib>Halpern, Norman B.</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Cancer</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kheir, Sonia M.</au><au>Halpern, Norman B.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Paraganglioma of the duodenum in association with congenital neurofibromatosis possible relationship</atitle><jtitle>Cancer</jtitle><addtitle>Cancer</addtitle><date>1984-06-01</date><risdate>1984</risdate><volume>53</volume><issue>11</issue><spage>2491</spage><epage>2496</epage><pages>2491-2496</pages><issn>0008-543X</issn><eissn>1097-0142</eissn><coden>CANCAR</coden><abstract>A case of a duodenal paraganglioma in a patient with von Recklinghausen's disease is presented, along with a review of the common clinical features of the 26 cases of duodenal paraganglioma and related neurogenic tumors reported in the literature. There was no reported evidence of recurrence or metastasis. Local excision was the most commonly employed method of treatment. It is proposed that duodenal paraganglioma with its admixed components and variable histologic features may represent hamartomatous hyperplasia of the paraganglia and the supporting neuroid tissue in this area. This would explain the benign behavior of these tumors as compared with carcinoids. Its association, in this case, with neurofibromatosis supports the neural crest origin of duodenal paragangliomas.</abstract><cop>New York</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>6201261</pmid><doi>10.1002/1097-0142(19840601)53:11<2491::AID-CNCR2820531122>3.0.CO;2-S</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record> |
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| identifier | ISSN: 0008-543X |
| ispartof | Cancer, 1984-06, Vol.53 (11), p.2491-2496 |
| issn | 0008-543X 1097-0142 |
| language | eng |
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| source | EZB Electronic Journals Library |
| subjects | Biological and medical sciences Cytoplasmic Granules - ultrastructure Duodenal Neoplasms - pathology Duodenal Neoplasms - ultrastructure Female Gastroenterology. Liver. Pancreas. Abdomen Humans Male Medical sciences Microscopy, Electron Middle Aged Neoplasms, Multiple Primary Neurofibromatosis 1 - congenital Neurofibromatosis 1 - pathology Paraganglioma - pathology Paraganglioma - ultrastructure Sex Factors Skin Neoplasms - congenital Skin Neoplasms - pathology Staining and Labeling Stomach. Duodenum. Small intestine. Colon. Rectum. Anus Tumors |
| title | Paraganglioma of the duodenum in association with congenital neurofibromatosis possible relationship |
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