A rare case of pulmonary cryptococcal inflammatory myofibroblastic tumor diagnosed by fine needle aspiration cytology
In a recent outbreak in British Columbia (BC), Canada, Cryptococcus gattii, a rare species of Cryptococcus, was noted to affect primarily immunocompetent hosts and cause limited pulmonary or CNS disease. We herein report a rare case of a pulmonary inflammatory myofibroblastic tumor caused by a Crypt...
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Veröffentlicht in: | Diagnostic cytopathology 2010-06, Vol.38 (6), p.447-451 |
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description | In a recent outbreak in British Columbia (BC), Canada, Cryptococcus gattii, a rare species of Cryptococcus, was noted to affect primarily immunocompetent hosts and cause limited pulmonary or CNS disease. We herein report a rare case of a pulmonary inflammatory myofibroblastic tumor caused by a Cryptococcus infection, presumed to be of the gattii species, in a 20‐year‐old immunocompetent college student from Vancouver, BC who presented with a large lung mass. The diagnosis was first made on the fine needle aspirate (FNA) material and was confirmed on the concurrent histologic core biopsy. Cryptococcal inflammatory myofibroblastic tumors have been reported, but neither in the lung nor in the setting of an immunocompetent host. Pulmonary cryptococcosis should therefore be considered in the differential diagnosis of a lung mass, even in an immunocompetent host, especially if the clinical history reveals recent travel to British Columbia where Cryptococcus gattii is endemic. Diagn. Cytopathol. 2010. © 2009 Wiley‐Liss, Inc. |
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We herein report a rare case of a pulmonary inflammatory myofibroblastic tumor caused by a Cryptococcus infection, presumed to be of the gattii species, in a 20‐year‐old immunocompetent college student from Vancouver, BC who presented with a large lung mass. The diagnosis was first made on the fine needle aspirate (FNA) material and was confirmed on the concurrent histologic core biopsy. Cryptococcal inflammatory myofibroblastic tumors have been reported, but neither in the lung nor in the setting of an immunocompetent host. Pulmonary cryptococcosis should therefore be considered in the differential diagnosis of a lung mass, even in an immunocompetent host, especially if the clinical history reveals recent travel to British Columbia where Cryptococcus gattii is endemic. Diagn. Cytopathol. 2010. © 2009 Wiley‐Liss, Inc.</description><identifier>ISSN: 8755-1039</identifier><identifier>EISSN: 1097-0339</identifier><identifier>DOI: 10.1002/dc.21259</identifier><identifier>PMID: 19937947</identifier><language>eng</language><publisher>Hoboken: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>Antifungal Agents - therapeutic use ; Biopsy, Fine-Needle ; cryptococcosis ; Cryptococcosis - drug therapy ; Cryptococcosis - pathology ; Cryptococcus ; Cryptococcus gattii ; cytology ; Female ; Fluconazole - therapeutic use ; Humans ; inflammatory myofibroblastic tumor ; lung ; Plasma Cell Granuloma, Pulmonary - drug therapy ; Plasma Cell Granuloma, Pulmonary - pathology ; Young Adult</subject><ispartof>Diagnostic cytopathology, 2010-06, Vol.38 (6), p.447-451</ispartof><rights>Copyright © 2009 Wiley‐Liss, Inc.</rights><rights>(c) 2009 Wiley-Liss, Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3909-1505884296d7c665ae61246aef3bfa65239d7fc5aec1d85499a1f13375f101513</citedby><cites>FETCH-LOGICAL-c3909-1505884296d7c665ae61246aef3bfa65239d7fc5aec1d85499a1f13375f101513</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fdc.21259$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fdc.21259$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19937947$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kushner, Yael B.</creatorcontrib><creatorcontrib>Brimo, Fadi</creatorcontrib><creatorcontrib>Schwartzman, Kevin</creatorcontrib><creatorcontrib>Auger, Manon</creatorcontrib><title>A rare case of pulmonary cryptococcal inflammatory myofibroblastic tumor diagnosed by fine needle aspiration cytology</title><title>Diagnostic cytopathology</title><addtitle>Diagn. Cytopathol</addtitle><description>In a recent outbreak in British Columbia (BC), Canada, Cryptococcus gattii, a rare species of Cryptococcus, was noted to affect primarily immunocompetent hosts and cause limited pulmonary or CNS disease. We herein report a rare case of a pulmonary inflammatory myofibroblastic tumor caused by a Cryptococcus infection, presumed to be of the gattii species, in a 20‐year‐old immunocompetent college student from Vancouver, BC who presented with a large lung mass. The diagnosis was first made on the fine needle aspirate (FNA) material and was confirmed on the concurrent histologic core biopsy. Cryptococcal inflammatory myofibroblastic tumors have been reported, but neither in the lung nor in the setting of an immunocompetent host. Pulmonary cryptococcosis should therefore be considered in the differential diagnosis of a lung mass, even in an immunocompetent host, especially if the clinical history reveals recent travel to British Columbia where Cryptococcus gattii is endemic. Diagn. Cytopathol. 2010. © 2009 Wiley‐Liss, Inc.</description><subject>Antifungal Agents - therapeutic use</subject><subject>Biopsy, Fine-Needle</subject><subject>cryptococcosis</subject><subject>Cryptococcosis - drug therapy</subject><subject>Cryptococcosis - pathology</subject><subject>Cryptococcus</subject><subject>Cryptococcus gattii</subject><subject>cytology</subject><subject>Female</subject><subject>Fluconazole - therapeutic use</subject><subject>Humans</subject><subject>inflammatory myofibroblastic tumor</subject><subject>lung</subject><subject>Plasma Cell Granuloma, Pulmonary - drug therapy</subject><subject>Plasma Cell Granuloma, Pulmonary - pathology</subject><subject>Young Adult</subject><issn>8755-1039</issn><issn>1097-0339</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqF0U1v1DAQBmALUdGlReIXIN_KJa0nju31sezSgtSWCxUSF8vxR-XWiYOdqOTfE9ilnCpOI808eqWZQegtkFMgpD6z5rSGmskXaAVEiopQKl-i1VowVgGh8hC9LuWeECJr4K_QIUhJhWzECk3nOOvssNHF4eTxMMUu9TrP2OR5GJNJxuiIQ--j7jo9pmXSzcmHNqc26jIGg8epSxnboO_6VJzF7Yx96B3unbPRYV2GkPUYUo_NPKaY7uZjdOB1LO7Nvh6h24uPXzefqqsvl58351eVoZLIChhh63VTS26F4Zxpx6FuuHaetl5zVlNphTdL34Bds0ZKDR4oFcwDAQb0CJ3scoecfkyujKoLxbgYde_SVJRomKhpQ8n_JaUUBAO-yPc7aXIqJTuvhhy65WIKiPr9DWWN-vONhb7bh05t5-w_uD__AqodeAzRzc8Gqe3mb-DehzK6n09e5wfFxbK2-nZzqbbfP3C43l4oSn8BTEKi2w</recordid><startdate>201006</startdate><enddate>201006</enddate><creator>Kushner, Yael B.</creator><creator>Brimo, Fadi</creator><creator>Schwartzman, Kevin</creator><creator>Auger, Manon</creator><general>Wiley Subscription Services, Inc., A Wiley Company</general><scope>BSCLL</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><scope>M7N</scope></search><sort><creationdate>201006</creationdate><title>A rare case of pulmonary cryptococcal inflammatory myofibroblastic tumor diagnosed by fine needle aspiration cytology</title><author>Kushner, Yael B. ; Brimo, Fadi ; Schwartzman, Kevin ; Auger, Manon</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3909-1505884296d7c665ae61246aef3bfa65239d7fc5aec1d85499a1f13375f101513</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>Antifungal Agents - therapeutic use</topic><topic>Biopsy, Fine-Needle</topic><topic>cryptococcosis</topic><topic>Cryptococcosis - drug therapy</topic><topic>Cryptococcosis - pathology</topic><topic>Cryptococcus</topic><topic>Cryptococcus gattii</topic><topic>cytology</topic><topic>Female</topic><topic>Fluconazole - therapeutic use</topic><topic>Humans</topic><topic>inflammatory myofibroblastic tumor</topic><topic>lung</topic><topic>Plasma Cell Granuloma, Pulmonary - drug therapy</topic><topic>Plasma Cell Granuloma, Pulmonary - pathology</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kushner, Yael B.</creatorcontrib><creatorcontrib>Brimo, Fadi</creatorcontrib><creatorcontrib>Schwartzman, Kevin</creatorcontrib><creatorcontrib>Auger, Manon</creatorcontrib><collection>Istex</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><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><jtitle>Diagnostic cytopathology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kushner, Yael B.</au><au>Brimo, Fadi</au><au>Schwartzman, Kevin</au><au>Auger, Manon</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A rare case of pulmonary cryptococcal inflammatory myofibroblastic tumor diagnosed by fine needle aspiration cytology</atitle><jtitle>Diagnostic cytopathology</jtitle><addtitle>Diagn. Cytopathol</addtitle><date>2010-06</date><risdate>2010</risdate><volume>38</volume><issue>6</issue><spage>447</spage><epage>451</epage><pages>447-451</pages><issn>8755-1039</issn><eissn>1097-0339</eissn><abstract>In a recent outbreak in British Columbia (BC), Canada, Cryptococcus gattii, a rare species of Cryptococcus, was noted to affect primarily immunocompetent hosts and cause limited pulmonary or CNS disease. We herein report a rare case of a pulmonary inflammatory myofibroblastic tumor caused by a Cryptococcus infection, presumed to be of the gattii species, in a 20‐year‐old immunocompetent college student from Vancouver, BC who presented with a large lung mass. The diagnosis was first made on the fine needle aspirate (FNA) material and was confirmed on the concurrent histologic core biopsy. Cryptococcal inflammatory myofibroblastic tumors have been reported, but neither in the lung nor in the setting of an immunocompetent host. Pulmonary cryptococcosis should therefore be considered in the differential diagnosis of a lung mass, even in an immunocompetent host, especially if the clinical history reveals recent travel to British Columbia where Cryptococcus gattii is endemic. Diagn. Cytopathol. 2010. © 2009 Wiley‐Liss, Inc.</abstract><cop>Hoboken</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>19937947</pmid><doi>10.1002/dc.21259</doi><tpages>5</tpages></addata></record> |
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subjects | Antifungal Agents - therapeutic use Biopsy, Fine-Needle cryptococcosis Cryptococcosis - drug therapy Cryptococcosis - pathology Cryptococcus Cryptococcus gattii cytology Female Fluconazole - therapeutic use Humans inflammatory myofibroblastic tumor lung Plasma Cell Granuloma, Pulmonary - drug therapy Plasma Cell Granuloma, Pulmonary - pathology Young Adult |
title | A rare case of pulmonary cryptococcal inflammatory myofibroblastic tumor diagnosed by fine needle aspiration cytology |
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