Aggressive angiomyxoma presenting as a vulval polyp
Aggressive angiomyxoma is a rare, locally invasive mesenchymal tumor, occurring predominantly in the pelvic-perineal region of adults and carries a high risk for local relapse and hence the need to differentiate it from the other mesenchymal tumors occurring in this region. Presentation as a peduncu...
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Veröffentlicht in: | Indian journal of cancer 2007-04, Vol.44 (2), p.87-89 |
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creator | Srinivasan, R Mohapatra, Nachiketa Malhotra, Saurabh Rao, Sharath Kumar J |
description | Aggressive angiomyxoma is a rare, locally invasive mesenchymal tumor, occurring predominantly in the pelvic-perineal region of adults and carries a high risk for local relapse and hence the need to differentiate it from the other mesenchymal tumors occurring in this region. Presentation as a pedunculated polyp, like in our case, is unusual for this rare tumor. Except for positive surgical margins, there are no clinical or histological means for predicting the tumor recurrence. A diligent long-term follow-up is mandatory. Though rare, this tumor needs to be considered in the differential diagnosis of vulval polyps. |
doi_str_mv | 10.4103/0019-509X.35815 |
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Presentation as a pedunculated polyp, like in our case, is unusual for this rare tumor. Except for positive surgical margins, there are no clinical or histological means for predicting the tumor recurrence. A diligent long-term follow-up is mandatory. Though rare, this tumor needs to be considered in the differential diagnosis of vulval polyps.</description><identifier>ISSN: 0019-509X</identifier><identifier>EISSN: 1998-4774</identifier><identifier>DOI: 10.4103/0019-509X.35815</identifier><identifier>PMID: 17938485</identifier><language>eng</language><publisher>India: Medknow Publications and Media Pvt. 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Presentation as a pedunculated polyp, like in our case, is unusual for this rare tumor. Except for positive surgical margins, there are no clinical or histological means for predicting the tumor recurrence. A diligent long-term follow-up is mandatory. Though rare, this tumor needs to be considered in the differential diagnosis of vulval polyps.</description><subject>Adult</subject><subject>Care and treatment</subject><subject>Case studies</subject><subject>Development and progression</subject><subject>Diagnosis</subject><subject>Diagnosis, Differential</subject><subject>Female</subject><subject>Genetic aspects</subject><subject>Humans</subject><subject>Immunohistochemistry</subject><subject>Leiomyoma - pathology</subject><subject>Myxoma - diagnosis</subject><subject>Myxoma - metabolism</subject><subject>Myxoma - pathology</subject><subject>Myxoma - surgery</subject><subject>Polyps - diagnosis</subject><subject>Polyps - metabolism</subject><subject>Polyps - pathology</subject><subject>Polyps - surgery</subject><subject>Receptors, Progesterone - metabolism</subject><subject>Vulvar cancer</subject><subject>Vulvar Neoplasms - diagnosis</subject><subject>Vulvar Neoplasms - metabolism</subject><subject>Vulvar Neoplasms - pathology</subject><subject>Vulvar Neoplasms - surgery</subject><issn>0019-509X</issn><issn>1998-4774</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2007</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>8G5</sourceid><sourceid>BENPR</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNptkcFr2zAUh8XoWNNu592K6SE3p5Il2dIxlK4tFHbZYDch28-Ogiy5kh2a_37KErZ2VDoInr7f4z0-hL4SvGIE0xuMicw5lr9WlAvCP6AFkVLkrKrYGVr8_T1HFzFuMS5owcQndE4qSQUTfIHouu8DxGh2kGnXGz_sX_ygszEVwU3G9ZmOmc52s91pm43e7sfP6GOnbYQvp_cS_fx29-P2IX_6fv94u37KGypKnmtCSS0Z8DKdrhKCypLXFJct1R0QXONOSlJXUDdcMCKg0ZgVreC1FNBSRi_R8th3DP55hjipwcQGrNUO_BxVmToyXtIEXv8Hbv0cXJpNFbTkRGJSJCg_Qr22oIzr_BR004ODoK130JlUXpMKYywqeeBX7_DptjCY5t3A8lVgA9pOm-jtPBnv4lvw5gg2wccYoFNjMIMOe0WwOmhVB3HqIE790ZoSV6cF53qA9h9_8kh_A7DKmZ8</recordid><startdate>20070401</startdate><enddate>20070401</enddate><creator>Srinivasan, R</creator><creator>Mohapatra, Nachiketa</creator><creator>Malhotra, Saurabh</creator><creator>Rao, Sharath Kumar J</creator><general>Medknow Publications and Media Pvt. 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pathology</topic><topic>Myxoma - diagnosis</topic><topic>Myxoma - metabolism</topic><topic>Myxoma - pathology</topic><topic>Myxoma - surgery</topic><topic>Polyps - diagnosis</topic><topic>Polyps - metabolism</topic><topic>Polyps - pathology</topic><topic>Polyps - surgery</topic><topic>Receptors, Progesterone - metabolism</topic><topic>Vulvar cancer</topic><topic>Vulvar Neoplasms - diagnosis</topic><topic>Vulvar Neoplasms - metabolism</topic><topic>Vulvar Neoplasms - pathology</topic><topic>Vulvar Neoplasms - surgery</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Srinivasan, R</creatorcontrib><creatorcontrib>Mohapatra, Nachiketa</creatorcontrib><creatorcontrib>Malhotra, Saurabh</creatorcontrib><creatorcontrib>Rao, Sharath Kumar J</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>AUTh Library subscriptions: ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>ProQuest Research Library</collection><collection>Research Library (Corporate)</collection><collection>Publicly Available Content (ProQuest)</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - 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Presentation as a pedunculated polyp, like in our case, is unusual for this rare tumor. Except for positive surgical margins, there are no clinical or histological means for predicting the tumor recurrence. A diligent long-term follow-up is mandatory. Though rare, this tumor needs to be considered in the differential diagnosis of vulval polyps.</abstract><cop>India</cop><pub>Medknow Publications and Media Pvt. Ltd</pub><pmid>17938485</pmid><doi>10.4103/0019-509X.35815</doi><tpages>3</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adult Care and treatment Case studies Development and progression Diagnosis Diagnosis, Differential Female Genetic aspects Humans Immunohistochemistry Leiomyoma - pathology Myxoma - diagnosis Myxoma - metabolism Myxoma - pathology Myxoma - surgery Polyps - diagnosis Polyps - metabolism Polyps - pathology Polyps - surgery Receptors, Progesterone - metabolism Vulvar cancer Vulvar Neoplasms - diagnosis Vulvar Neoplasms - metabolism Vulvar Neoplasms - pathology Vulvar Neoplasms - surgery |
title | Aggressive angiomyxoma presenting as a vulval polyp |
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