Paroxysmal nocturnal hemoglobinuria and myelodysplastic syndrome: a case report
Paroxysmal nocturnal hemoglobinuria is a rare clonal non-malignant disease, linked to an acquired PIG-A gene mutation. We report the case of 81 years old patient hospitalized for articular ache, swelling and temporal arteries' induration in which we diagnose PNH associated with refractory cytop...
Gespeichert in:
Veröffentlicht in: | Annales de biologie clinique (Paris) 2016-01, Vol.74 (1), p.106-109 |
---|---|
Hauptverfasser: | , , |
Format: | Artikel |
Sprache: | fre |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 109 |
---|---|
container_issue | 1 |
container_start_page | 106 |
container_title | Annales de biologie clinique (Paris) |
container_volume | 74 |
creator | Le Guyader, Maïlys Pineau-Vincent, Fabienne Lemaire, Pierre |
description | Paroxysmal nocturnal hemoglobinuria is a rare clonal non-malignant disease, linked to an acquired PIG-A gene mutation. We report the case of 81 years old patient hospitalized for articular ache, swelling and temporal arteries' induration in which we diagnose PNH associated with refractory cytopenia with multilineage dysplasia. |
doi_str_mv | 10.1684/abc.2015.1117 |
format | Article |
fullrecord | <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_proquest_miscellaneous_1797872305</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>1797872305</sourcerecordid><originalsourceid>FETCH-LOGICAL-p141t-66ad0fc00fa6375b2a54a878f263fedbdbf014fd2be4bec38ea5dc6f51f9ec473</originalsourceid><addsrcrecordid>eNo1kDtPwzAURi0kREthZEUZWVJ8bcdO2VDFS6pUBpij6xcEOXGwE4n8eypRpvMNR99wCLkCugZZi1vUZs0oVGsAUCdkCZuKlhKALch5zl-UAqs5PyMLJpUQjNdLsn_FFH_m3GEo-mjGKfWH9em6-BGibvsptVhgb4tudiHaOQ8B89iaIs-9TbFzdwUWBrMrkhtiGi_IqceQ3eWRK_L--PC2fS53-6eX7f2uHEDAWEqJlnpDqUfJVaUZVgJrVXsmuXdWW-0pCG-ZdkI7w2uHlTXSV-A3zgjFV-Tm73dI8XtyeWy6NhsXAvYuTrkBtVG1YpxWB_X6qE66c7YZUtthmpv_CPwXaTde3g</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1797872305</pqid></control><display><type>article</type><title>Paroxysmal nocturnal hemoglobinuria and myelodysplastic syndrome: a case report</title><source>MEDLINE</source><source>EZB-FREE-00999 freely available EZB journals</source><creator>Le Guyader, Maïlys ; Pineau-Vincent, Fabienne ; Lemaire, Pierre</creator><creatorcontrib>Le Guyader, Maïlys ; Pineau-Vincent, Fabienne ; Lemaire, Pierre</creatorcontrib><description>Paroxysmal nocturnal hemoglobinuria is a rare clonal non-malignant disease, linked to an acquired PIG-A gene mutation. We report the case of 81 years old patient hospitalized for articular ache, swelling and temporal arteries' induration in which we diagnose PNH associated with refractory cytopenia with multilineage dysplasia.</description><identifier>EISSN: 1950-6112</identifier><identifier>DOI: 10.1684/abc.2015.1117</identifier><identifier>PMID: 26744238</identifier><language>fre</language><publisher>France</publisher><subject>Aged, 80 and over ; Diabetes Mellitus, Type 2 - complications ; Hemoglobinuria, Paroxysmal - complications ; Hemoglobinuria, Paroxysmal - pathology ; Humans ; Male ; Myelodysplastic Syndromes - complications ; Myelodysplastic Syndromes - pathology ; Urolithiasis - complications</subject><ispartof>Annales de biologie clinique (Paris), 2016-01, Vol.74 (1), p.106-109</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/26744238$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Le Guyader, Maïlys</creatorcontrib><creatorcontrib>Pineau-Vincent, Fabienne</creatorcontrib><creatorcontrib>Lemaire, Pierre</creatorcontrib><title>Paroxysmal nocturnal hemoglobinuria and myelodysplastic syndrome: a case report</title><title>Annales de biologie clinique (Paris)</title><addtitle>Ann Biol Clin (Paris)</addtitle><description>Paroxysmal nocturnal hemoglobinuria is a rare clonal non-malignant disease, linked to an acquired PIG-A gene mutation. We report the case of 81 years old patient hospitalized for articular ache, swelling and temporal arteries' induration in which we diagnose PNH associated with refractory cytopenia with multilineage dysplasia.</description><subject>Aged, 80 and over</subject><subject>Diabetes Mellitus, Type 2 - complications</subject><subject>Hemoglobinuria, Paroxysmal - complications</subject><subject>Hemoglobinuria, Paroxysmal - pathology</subject><subject>Humans</subject><subject>Male</subject><subject>Myelodysplastic Syndromes - complications</subject><subject>Myelodysplastic Syndromes - pathology</subject><subject>Urolithiasis - complications</subject><issn>1950-6112</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNo1kDtPwzAURi0kREthZEUZWVJ8bcdO2VDFS6pUBpij6xcEOXGwE4n8eypRpvMNR99wCLkCugZZi1vUZs0oVGsAUCdkCZuKlhKALch5zl-UAqs5PyMLJpUQjNdLsn_FFH_m3GEo-mjGKfWH9em6-BGibvsptVhgb4tudiHaOQ8B89iaIs-9TbFzdwUWBrMrkhtiGi_IqceQ3eWRK_L--PC2fS53-6eX7f2uHEDAWEqJlnpDqUfJVaUZVgJrVXsmuXdWW-0pCG-ZdkI7w2uHlTXSV-A3zgjFV-Tm73dI8XtyeWy6NhsXAvYuTrkBtVG1YpxWB_X6qE66c7YZUtthmpv_CPwXaTde3g</recordid><startdate>201601</startdate><enddate>201601</enddate><creator>Le Guyader, Maïlys</creator><creator>Pineau-Vincent, Fabienne</creator><creator>Lemaire, Pierre</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>201601</creationdate><title>Paroxysmal nocturnal hemoglobinuria and myelodysplastic syndrome: a case report</title><author>Le Guyader, Maïlys ; Pineau-Vincent, Fabienne ; Lemaire, Pierre</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p141t-66ad0fc00fa6375b2a54a878f263fedbdbf014fd2be4bec38ea5dc6f51f9ec473</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>fre</language><creationdate>2016</creationdate><topic>Aged, 80 and over</topic><topic>Diabetes Mellitus, Type 2 - complications</topic><topic>Hemoglobinuria, Paroxysmal - complications</topic><topic>Hemoglobinuria, Paroxysmal - pathology</topic><topic>Humans</topic><topic>Male</topic><topic>Myelodysplastic Syndromes - complications</topic><topic>Myelodysplastic Syndromes - pathology</topic><topic>Urolithiasis - complications</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Le Guyader, Maïlys</creatorcontrib><creatorcontrib>Pineau-Vincent, Fabienne</creatorcontrib><creatorcontrib>Lemaire, Pierre</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>Le Guyader, Maïlys</au><au>Pineau-Vincent, Fabienne</au><au>Lemaire, Pierre</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Paroxysmal nocturnal hemoglobinuria and myelodysplastic syndrome: a case report</atitle><jtitle>Annales de biologie clinique (Paris)</jtitle><addtitle>Ann Biol Clin (Paris)</addtitle><date>2016-01</date><risdate>2016</risdate><volume>74</volume><issue>1</issue><spage>106</spage><epage>109</epage><pages>106-109</pages><eissn>1950-6112</eissn><abstract>Paroxysmal nocturnal hemoglobinuria is a rare clonal non-malignant disease, linked to an acquired PIG-A gene mutation. We report the case of 81 years old patient hospitalized for articular ache, swelling and temporal arteries' induration in which we diagnose PNH associated with refractory cytopenia with multilineage dysplasia.</abstract><cop>France</cop><pmid>26744238</pmid><doi>10.1684/abc.2015.1117</doi><tpages>4</tpages></addata></record> |
fulltext | fulltext |
identifier | EISSN: 1950-6112 |
ispartof | Annales de biologie clinique (Paris), 2016-01, Vol.74 (1), p.106-109 |
issn | 1950-6112 |
language | fre |
recordid | cdi_proquest_miscellaneous_1797872305 |
source | MEDLINE; EZB-FREE-00999 freely available EZB journals |
subjects | Aged, 80 and over Diabetes Mellitus, Type 2 - complications Hemoglobinuria, Paroxysmal - complications Hemoglobinuria, Paroxysmal - pathology Humans Male Myelodysplastic Syndromes - complications Myelodysplastic Syndromes - pathology Urolithiasis - complications |
title | Paroxysmal nocturnal hemoglobinuria and myelodysplastic syndrome: a case report |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-05T14%3A34%3A35IST&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=Paroxysmal%20nocturnal%20hemoglobinuria%20and%20myelodysplastic%20syndrome:%20a%20case%20report&rft.jtitle=Annales%20de%20biologie%20clinique%20(Paris)&rft.au=Le%20Guyader,%20Ma%C3%AFlys&rft.date=2016-01&rft.volume=74&rft.issue=1&rft.spage=106&rft.epage=109&rft.pages=106-109&rft.eissn=1950-6112&rft_id=info:doi/10.1684/abc.2015.1117&rft_dat=%3Cproquest_pubme%3E1797872305%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=1797872305&rft_id=info:pmid/26744238&rfr_iscdi=true |