Another case of the rare complications of chronic lymphocytic leukemia: angioedema
Angioedema is a rare but may be serious (laryngeal edema). This is a recurrent edema, subcutaneous and/or submucosal, whose cause is a hereditary or acquired deficiency in C1 inhibiteur (C1 inhibitor fraction of complement). We present the case of a 56 years old patient who showed recurrent episodes...
Gespeichert in:
| Veröffentlicht in: | Annales de biologie clinique (Paris) 2014-07, Vol.72 (4), p.479-481 |
|---|---|
| Hauptverfasser: | , , , , , , , , , , |
| Format: | Artikel |
| Sprache: | fre |
| Schlagworte: | |
| Online-Zugang: | Volltext |
| Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
| container_end_page | 481 |
|---|---|
| container_issue | 4 |
| container_start_page | 479 |
| container_title | Annales de biologie clinique (Paris) |
| container_volume | 72 |
| creator | Tlamçani, Imane Benjelloun, Salma Yahyaoui, Ghita Moudden, Mohamed Karim Lahlou, Hazar El Boukhrissi, Fatima Amrani Hassani, Moncef El Haouri, Mohamed El Baaj, Mohamed Balouch, Lhoussine Bamou, Youssef |
| description | Angioedema is a rare but may be serious (laryngeal edema). This is a recurrent edema, subcutaneous and/or submucosal, whose cause is a hereditary or acquired deficiency in C1 inhibiteur (C1 inhibitor fraction of complement). We present the case of a 56 years old patient who showed recurrent episodes of swelling of the face and hands in association with chronic lymphocytic leukemia stage A. The exploration of the complement pathway has allowed retaining the diagnosis of acquired angioedema type I. The association of angioedema and lymphoproliferative syndrome is rare; we present this interesting case to discuss it from the literature data. |
| doi_str_mv | 10.1684/abc.2014.0966 |
| format | Article |
| fullrecord | <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_proquest_miscellaneous_1666297159</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>1666297159</sourcerecordid><originalsourceid>FETCH-LOGICAL-p211t-af08ccf7bba58003f9e132820bb2b309202eabee8f41a65c676d137637f000153</originalsourceid><addsrcrecordid>eNo1UMFKAzEUDILYWj16lRy9bM1LutmNt1KsCgVB9Lwk6YuNbjZrsnvo39tiPc0MMwzMEHIDbA6yXtxrY-ecwWLOlJRnZAqqZIUE4BNymfMXY8BrIS7IhJcAqmbVlLwtuzjsMFGrM9Lo6EHQpBNSG0PfeqsHH7t8dOwuxc5b2u5Dv4t2Pxw5jt8YvH6guvv0EbcY9BU5d7rNeH3CGflYP76vnovN69PLarkpeg4wFNqx2lpXGaPLmjHhFILgNWfGcCOY4oyjNoi1W4CWpZWV3IKopKgcOywpxYzc_fX2Kf6MmIcm-GyxbXWHccwNSCm5qqBUh-jtKTqagNumTz7otG_-fxC_KTBdRQ</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1666297159</pqid></control><display><type>article</type><title>Another case of the rare complications of chronic lymphocytic leukemia: angioedema</title><source>MEDLINE</source><source>EZB-FREE-00999 freely available EZB journals</source><creator>Tlamçani, Imane ; Benjelloun, Salma ; Yahyaoui, Ghita ; Moudden, Mohamed Karim ; Lahlou, Hazar ; El Boukhrissi, Fatima ; Amrani Hassani, Moncef ; El Haouri, Mohamed ; El Baaj, Mohamed ; Balouch, Lhoussine ; Bamou, Youssef</creator><creatorcontrib>Tlamçani, Imane ; Benjelloun, Salma ; Yahyaoui, Ghita ; Moudden, Mohamed Karim ; Lahlou, Hazar ; El Boukhrissi, Fatima ; Amrani Hassani, Moncef ; El Haouri, Mohamed ; El Baaj, Mohamed ; Balouch, Lhoussine ; Bamou, Youssef</creatorcontrib><description>Angioedema is a rare but may be serious (laryngeal edema). This is a recurrent edema, subcutaneous and/or submucosal, whose cause is a hereditary or acquired deficiency in C1 inhibiteur (C1 inhibitor fraction of complement). We present the case of a 56 years old patient who showed recurrent episodes of swelling of the face and hands in association with chronic lymphocytic leukemia stage A. The exploration of the complement pathway has allowed retaining the diagnosis of acquired angioedema type I. The association of angioedema and lymphoproliferative syndrome is rare; we present this interesting case to discuss it from the literature data.</description><identifier>EISSN: 1950-6112</identifier><identifier>DOI: 10.1684/abc.2014.0966</identifier><identifier>PMID: 25119807</identifier><language>fre</language><publisher>France</publisher><subject>Angioedema - etiology ; Humans ; Leukemia, Lymphocytic, Chronic, B-Cell - complications ; Male ; Middle Aged</subject><ispartof>Annales de biologie clinique (Paris), 2014-07, Vol.72 (4), p.479-481</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25119807$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Tlamçani, Imane</creatorcontrib><creatorcontrib>Benjelloun, Salma</creatorcontrib><creatorcontrib>Yahyaoui, Ghita</creatorcontrib><creatorcontrib>Moudden, Mohamed Karim</creatorcontrib><creatorcontrib>Lahlou, Hazar</creatorcontrib><creatorcontrib>El Boukhrissi, Fatima</creatorcontrib><creatorcontrib>Amrani Hassani, Moncef</creatorcontrib><creatorcontrib>El Haouri, Mohamed</creatorcontrib><creatorcontrib>El Baaj, Mohamed</creatorcontrib><creatorcontrib>Balouch, Lhoussine</creatorcontrib><creatorcontrib>Bamou, Youssef</creatorcontrib><title>Another case of the rare complications of chronic lymphocytic leukemia: angioedema</title><title>Annales de biologie clinique (Paris)</title><addtitle>Ann Biol Clin (Paris)</addtitle><description>Angioedema is a rare but may be serious (laryngeal edema). This is a recurrent edema, subcutaneous and/or submucosal, whose cause is a hereditary or acquired deficiency in C1 inhibiteur (C1 inhibitor fraction of complement). We present the case of a 56 years old patient who showed recurrent episodes of swelling of the face and hands in association with chronic lymphocytic leukemia stage A. The exploration of the complement pathway has allowed retaining the diagnosis of acquired angioedema type I. The association of angioedema and lymphoproliferative syndrome is rare; we present this interesting case to discuss it from the literature data.</description><subject>Angioedema - etiology</subject><subject>Humans</subject><subject>Leukemia, Lymphocytic, Chronic, B-Cell - complications</subject><subject>Male</subject><subject>Middle Aged</subject><issn>1950-6112</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNo1UMFKAzEUDILYWj16lRy9bM1LutmNt1KsCgVB9Lwk6YuNbjZrsnvo39tiPc0MMwzMEHIDbA6yXtxrY-ecwWLOlJRnZAqqZIUE4BNymfMXY8BrIS7IhJcAqmbVlLwtuzjsMFGrM9Lo6EHQpBNSG0PfeqsHH7t8dOwuxc5b2u5Dv4t2Pxw5jt8YvH6guvv0EbcY9BU5d7rNeH3CGflYP76vnovN69PLarkpeg4wFNqx2lpXGaPLmjHhFILgNWfGcCOY4oyjNoi1W4CWpZWV3IKopKgcOywpxYzc_fX2Kf6MmIcm-GyxbXWHccwNSCm5qqBUh-jtKTqagNumTz7otG_-fxC_KTBdRQ</recordid><startdate>201407</startdate><enddate>201407</enddate><creator>Tlamçani, Imane</creator><creator>Benjelloun, Salma</creator><creator>Yahyaoui, Ghita</creator><creator>Moudden, Mohamed Karim</creator><creator>Lahlou, Hazar</creator><creator>El Boukhrissi, Fatima</creator><creator>Amrani Hassani, Moncef</creator><creator>El Haouri, Mohamed</creator><creator>El Baaj, Mohamed</creator><creator>Balouch, Lhoussine</creator><creator>Bamou, Youssef</creator><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7X8</scope></search><sort><creationdate>201407</creationdate><title>Another case of the rare complications of chronic lymphocytic leukemia: angioedema</title><author>Tlamçani, Imane ; Benjelloun, Salma ; Yahyaoui, Ghita ; Moudden, Mohamed Karim ; Lahlou, Hazar ; El Boukhrissi, Fatima ; Amrani Hassani, Moncef ; El Haouri, Mohamed ; El Baaj, Mohamed ; Balouch, Lhoussine ; Bamou, Youssef</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p211t-af08ccf7bba58003f9e132820bb2b309202eabee8f41a65c676d137637f000153</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>fre</language><creationdate>2014</creationdate><topic>Angioedema - etiology</topic><topic>Humans</topic><topic>Leukemia, Lymphocytic, Chronic, B-Cell - complications</topic><topic>Male</topic><topic>Middle Aged</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Tlamçani, Imane</creatorcontrib><creatorcontrib>Benjelloun, Salma</creatorcontrib><creatorcontrib>Yahyaoui, Ghita</creatorcontrib><creatorcontrib>Moudden, Mohamed Karim</creatorcontrib><creatorcontrib>Lahlou, Hazar</creatorcontrib><creatorcontrib>El Boukhrissi, Fatima</creatorcontrib><creatorcontrib>Amrani Hassani, Moncef</creatorcontrib><creatorcontrib>El Haouri, Mohamed</creatorcontrib><creatorcontrib>El Baaj, Mohamed</creatorcontrib><creatorcontrib>Balouch, Lhoussine</creatorcontrib><creatorcontrib>Bamou, Youssef</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>MEDLINE - Academic</collection><jtitle>Annales de biologie clinique (Paris)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Tlamçani, Imane</au><au>Benjelloun, Salma</au><au>Yahyaoui, Ghita</au><au>Moudden, Mohamed Karim</au><au>Lahlou, Hazar</au><au>El Boukhrissi, Fatima</au><au>Amrani Hassani, Moncef</au><au>El Haouri, Mohamed</au><au>El Baaj, Mohamed</au><au>Balouch, Lhoussine</au><au>Bamou, Youssef</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Another case of the rare complications of chronic lymphocytic leukemia: angioedema</atitle><jtitle>Annales de biologie clinique (Paris)</jtitle><addtitle>Ann Biol Clin (Paris)</addtitle><date>2014-07</date><risdate>2014</risdate><volume>72</volume><issue>4</issue><spage>479</spage><epage>481</epage><pages>479-481</pages><eissn>1950-6112</eissn><abstract>Angioedema is a rare but may be serious (laryngeal edema). This is a recurrent edema, subcutaneous and/or submucosal, whose cause is a hereditary or acquired deficiency in C1 inhibiteur (C1 inhibitor fraction of complement). We present the case of a 56 years old patient who showed recurrent episodes of swelling of the face and hands in association with chronic lymphocytic leukemia stage A. The exploration of the complement pathway has allowed retaining the diagnosis of acquired angioedema type I. The association of angioedema and lymphoproliferative syndrome is rare; we present this interesting case to discuss it from the literature data.</abstract><cop>France</cop><pmid>25119807</pmid><doi>10.1684/abc.2014.0966</doi><tpages>3</tpages></addata></record> |
| fulltext | fulltext |
| identifier | EISSN: 1950-6112 |
| ispartof | Annales de biologie clinique (Paris), 2014-07, Vol.72 (4), p.479-481 |
| issn | 1950-6112 |
| language | fre |
| recordid | cdi_proquest_miscellaneous_1666297159 |
| source | MEDLINE; EZB-FREE-00999 freely available EZB journals |
| subjects | Angioedema - etiology Humans Leukemia, Lymphocytic, Chronic, B-Cell - complications Male Middle Aged |
| title | Another case of the rare complications of chronic lymphocytic leukemia: angioedema |
| url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-29T00%3A53%3A46IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Another%20case%20of%20the%20rare%20complications%20of%20chronic%20lymphocytic%20leukemia:%20angioedema&rft.jtitle=Annales%20de%20biologie%20clinique%20(Paris)&rft.au=Tlam%C3%A7ani,%20Imane&rft.date=2014-07&rft.volume=72&rft.issue=4&rft.spage=479&rft.epage=481&rft.pages=479-481&rft.eissn=1950-6112&rft_id=info:doi/10.1684/abc.2014.0966&rft_dat=%3Cproquest_pubme%3E1666297159%3C/proquest_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1666297159&rft_id=info:pmid/25119807&rfr_iscdi=true |