Successful treatment of eosinophilic granulomatosis with polyangiitis (EGPA; formerly Churg–Strauss syndrome) with rituximab in a case refractory to glucocorticoids, cyclophosphamide, and IVIG

Abstract A 44-year old woman with eosinophilic granulomatosis with polyangiitis (EGPA) developed sequential paralysis of different cranial nerves despite treatments including methylpredonisolone pulse therapy, intravenous immunoglobulins (IVIG), and cyclophosphamide. Infusions of rituximab ameliorat...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Modern rheumatology 2014-07, Vol.24 (4), p.685-687
Hauptverfasser: Umezawa, Natsuka, Kohsaka, Hitoshi, Nanki, Toshihiro, Watanabe, Kaori, Tanaka, Michi, Shane, Peter Y., Miyasaka, Nobuyuki
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 687
container_issue 4
container_start_page 685
container_title Modern rheumatology
container_volume 24
creator Umezawa, Natsuka
Kohsaka, Hitoshi
Nanki, Toshihiro
Watanabe, Kaori
Tanaka, Michi
Shane, Peter Y.
Miyasaka, Nobuyuki
description Abstract A 44-year old woman with eosinophilic granulomatosis with polyangiitis (EGPA) developed sequential paralysis of different cranial nerves despite treatments including methylpredonisolone pulse therapy, intravenous immunoglobulins (IVIG), and cyclophosphamide. Infusions of rituximab ameliorated her neurological symptoms and serological inflammatory findings. Rituximab, a specific B cell-targeting therapy, might offer an alternative for refractory EGPA with possible advantages of cost and ease of use compared to IVIG, which also targets (at least in part) B lymphocytes and immunoglobulin production.
doi_str_mv 10.3109/14397595.2013.874734
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_1542299276</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>1542299276</sourcerecordid><originalsourceid>FETCH-LOGICAL-c414t-4365fb47723ea802b6f1218de70eb9372f5d44c7edb1d7136b05ce9e8de2548e3</originalsourceid><addsrcrecordid>eNp9kd-K1DAUh4so7rr6BiIBb1bYGZMmaVoEYRnWcWBBYdXbkqan0yxpM5s_aO98B9_IR_FJTOmOiBdeJRy-38k5-bLsOcFrSnD1mjBaCV7xdY4JXZeCCcoeZKdzeSUKXD083hNzkj3x_hZjyquyepyd5IwTwTk9zX7eRKXA-y4aFBzIMMAYkO0QWK9He-i10QrtnRyjsYMMqerRVx16dLBmkuNe65Aq51fbj5dvUGfdAM5MaNNHt__1_cdNcDJ6j_w0ts4O8GrJOh3iNz3IBukRSaSkB-Sgc1IF6yYULNqbqKyyLmhldesvkJqUSeNYf-jloFu4QHJs0e7Lbvs0e9RJ4-HZ_XmWfX539WnzfnX9YbvbXF6vFCMsrBgteNcwIXIKssR5U3QkJ2ULAkNTUZF3vGVMCWgb0gpCiwZzBRUkIuesBHqWnS99D87eRfChHrRXYIwcwUZfE87yvKpyUST05T_orY1uTNPNVLJSUMwTxRZKOet92r8-uPQpbqoJrmfH9dFxPTuuF8cp9uK-eWwGaP-EjlIT8HYB9DgLkT1IE3olHfw1xv9e-A0BLLrP</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1544396305</pqid></control><display><type>article</type><title>Successful treatment of eosinophilic granulomatosis with polyangiitis (EGPA; formerly Churg–Strauss syndrome) with rituximab in a case refractory to glucocorticoids, cyclophosphamide, and IVIG</title><source>MEDLINE</source><source>Oxford University Press Journals All Titles (1996-Current)</source><creator>Umezawa, Natsuka ; Kohsaka, Hitoshi ; Nanki, Toshihiro ; Watanabe, Kaori ; Tanaka, Michi ; Shane, Peter Y. ; Miyasaka, Nobuyuki</creator><creatorcontrib>Umezawa, Natsuka ; Kohsaka, Hitoshi ; Nanki, Toshihiro ; Watanabe, Kaori ; Tanaka, Michi ; Shane, Peter Y. ; Miyasaka, Nobuyuki</creatorcontrib><description>Abstract A 44-year old woman with eosinophilic granulomatosis with polyangiitis (EGPA) developed sequential paralysis of different cranial nerves despite treatments including methylpredonisolone pulse therapy, intravenous immunoglobulins (IVIG), and cyclophosphamide. Infusions of rituximab ameliorated her neurological symptoms and serological inflammatory findings. Rituximab, a specific B cell-targeting therapy, might offer an alternative for refractory EGPA with possible advantages of cost and ease of use compared to IVIG, which also targets (at least in part) B lymphocytes and immunoglobulin production.</description><identifier>ISSN: 1439-7595</identifier><identifier>EISSN: 1439-7609</identifier><identifier>DOI: 10.3109/14397595.2013.874734</identifier><identifier>PMID: 24517553</identifier><language>eng</language><publisher>United States: Informa Healthcare</publisher><subject>Adult ; Antibodies, Monoclonal, Murine-Derived - therapeutic use ; Autoimmune diseases ; Churg-Strauss Syndrome - drug therapy ; Cyclophosphamide - therapeutic use ; Drug therapy ; Female ; Glucocorticoids - therapeutic use ; Humans ; Immunoglobulins, Intravenous - therapeutic use ; Immunologic Factors - therapeutic use ; Prescription drugs ; Retreatment ; Rituximab ; Treatment Outcome</subject><ispartof>Modern rheumatology, 2014-07, Vol.24 (4), p.685-687</ispartof><rights>2014 Japan College of Rheumatology 2014</rights><rights>Copyright Informa Healthcare Jul 2014</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c414t-4365fb47723ea802b6f1218de70eb9372f5d44c7edb1d7136b05ce9e8de2548e3</citedby><cites>FETCH-LOGICAL-c414t-4365fb47723ea802b6f1218de70eb9372f5d44c7edb1d7136b05ce9e8de2548e3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>315,781,785,27929,27930</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24517553$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Umezawa, Natsuka</creatorcontrib><creatorcontrib>Kohsaka, Hitoshi</creatorcontrib><creatorcontrib>Nanki, Toshihiro</creatorcontrib><creatorcontrib>Watanabe, Kaori</creatorcontrib><creatorcontrib>Tanaka, Michi</creatorcontrib><creatorcontrib>Shane, Peter Y.</creatorcontrib><creatorcontrib>Miyasaka, Nobuyuki</creatorcontrib><title>Successful treatment of eosinophilic granulomatosis with polyangiitis (EGPA; formerly Churg–Strauss syndrome) with rituximab in a case refractory to glucocorticoids, cyclophosphamide, and IVIG</title><title>Modern rheumatology</title><addtitle>Mod Rheumatol</addtitle><description>Abstract A 44-year old woman with eosinophilic granulomatosis with polyangiitis (EGPA) developed sequential paralysis of different cranial nerves despite treatments including methylpredonisolone pulse therapy, intravenous immunoglobulins (IVIG), and cyclophosphamide. Infusions of rituximab ameliorated her neurological symptoms and serological inflammatory findings. Rituximab, a specific B cell-targeting therapy, might offer an alternative for refractory EGPA with possible advantages of cost and ease of use compared to IVIG, which also targets (at least in part) B lymphocytes and immunoglobulin production.</description><subject>Adult</subject><subject>Antibodies, Monoclonal, Murine-Derived - therapeutic use</subject><subject>Autoimmune diseases</subject><subject>Churg-Strauss Syndrome - drug therapy</subject><subject>Cyclophosphamide - therapeutic use</subject><subject>Drug therapy</subject><subject>Female</subject><subject>Glucocorticoids - therapeutic use</subject><subject>Humans</subject><subject>Immunoglobulins, Intravenous - therapeutic use</subject><subject>Immunologic Factors - therapeutic use</subject><subject>Prescription drugs</subject><subject>Retreatment</subject><subject>Rituximab</subject><subject>Treatment Outcome</subject><issn>1439-7595</issn><issn>1439-7609</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kd-K1DAUh4so7rr6BiIBb1bYGZMmaVoEYRnWcWBBYdXbkqan0yxpM5s_aO98B9_IR_FJTOmOiBdeJRy-38k5-bLsOcFrSnD1mjBaCV7xdY4JXZeCCcoeZKdzeSUKXD083hNzkj3x_hZjyquyepyd5IwTwTk9zX7eRKXA-y4aFBzIMMAYkO0QWK9He-i10QrtnRyjsYMMqerRVx16dLBmkuNe65Aq51fbj5dvUGfdAM5MaNNHt__1_cdNcDJ6j_w0ts4O8GrJOh3iNz3IBukRSaSkB-Sgc1IF6yYULNqbqKyyLmhldesvkJqUSeNYf-jloFu4QHJs0e7Lbvs0e9RJ4-HZ_XmWfX539WnzfnX9YbvbXF6vFCMsrBgteNcwIXIKssR5U3QkJ2ULAkNTUZF3vGVMCWgb0gpCiwZzBRUkIuesBHqWnS99D87eRfChHrRXYIwcwUZfE87yvKpyUST05T_orY1uTNPNVLJSUMwTxRZKOet92r8-uPQpbqoJrmfH9dFxPTuuF8cp9uK-eWwGaP-EjlIT8HYB9DgLkT1IE3olHfw1xv9e-A0BLLrP</recordid><startdate>20140701</startdate><enddate>20140701</enddate><creator>Umezawa, Natsuka</creator><creator>Kohsaka, Hitoshi</creator><creator>Nanki, Toshihiro</creator><creator>Watanabe, Kaori</creator><creator>Tanaka, Michi</creator><creator>Shane, Peter Y.</creator><creator>Miyasaka, Nobuyuki</creator><general>Informa Healthcare</general><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>K9.</scope><scope>7X8</scope></search><sort><creationdate>20140701</creationdate><title>Successful treatment of eosinophilic granulomatosis with polyangiitis (EGPA; formerly Churg–Strauss syndrome) with rituximab in a case refractory to glucocorticoids, cyclophosphamide, and IVIG</title><author>Umezawa, Natsuka ; Kohsaka, Hitoshi ; Nanki, Toshihiro ; Watanabe, Kaori ; Tanaka, Michi ; Shane, Peter Y. ; Miyasaka, Nobuyuki</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c414t-4365fb47723ea802b6f1218de70eb9372f5d44c7edb1d7136b05ce9e8de2548e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Adult</topic><topic>Antibodies, Monoclonal, Murine-Derived - therapeutic use</topic><topic>Autoimmune diseases</topic><topic>Churg-Strauss Syndrome - drug therapy</topic><topic>Cyclophosphamide - therapeutic use</topic><topic>Drug therapy</topic><topic>Female</topic><topic>Glucocorticoids - therapeutic use</topic><topic>Humans</topic><topic>Immunoglobulins, Intravenous - therapeutic use</topic><topic>Immunologic Factors - therapeutic use</topic><topic>Prescription drugs</topic><topic>Retreatment</topic><topic>Rituximab</topic><topic>Treatment Outcome</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Umezawa, Natsuka</creatorcontrib><creatorcontrib>Kohsaka, Hitoshi</creatorcontrib><creatorcontrib>Nanki, Toshihiro</creatorcontrib><creatorcontrib>Watanabe, Kaori</creatorcontrib><creatorcontrib>Tanaka, Michi</creatorcontrib><creatorcontrib>Shane, Peter Y.</creatorcontrib><creatorcontrib>Miyasaka, Nobuyuki</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 Health &amp; Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><jtitle>Modern rheumatology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Umezawa, Natsuka</au><au>Kohsaka, Hitoshi</au><au>Nanki, Toshihiro</au><au>Watanabe, Kaori</au><au>Tanaka, Michi</au><au>Shane, Peter Y.</au><au>Miyasaka, Nobuyuki</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Successful treatment of eosinophilic granulomatosis with polyangiitis (EGPA; formerly Churg–Strauss syndrome) with rituximab in a case refractory to glucocorticoids, cyclophosphamide, and IVIG</atitle><jtitle>Modern rheumatology</jtitle><addtitle>Mod Rheumatol</addtitle><date>2014-07-01</date><risdate>2014</risdate><volume>24</volume><issue>4</issue><spage>685</spage><epage>687</epage><pages>685-687</pages><issn>1439-7595</issn><eissn>1439-7609</eissn><abstract>Abstract A 44-year old woman with eosinophilic granulomatosis with polyangiitis (EGPA) developed sequential paralysis of different cranial nerves despite treatments including methylpredonisolone pulse therapy, intravenous immunoglobulins (IVIG), and cyclophosphamide. Infusions of rituximab ameliorated her neurological symptoms and serological inflammatory findings. Rituximab, a specific B cell-targeting therapy, might offer an alternative for refractory EGPA with possible advantages of cost and ease of use compared to IVIG, which also targets (at least in part) B lymphocytes and immunoglobulin production.</abstract><cop>United States</cop><pub>Informa Healthcare</pub><pmid>24517553</pmid><doi>10.3109/14397595.2013.874734</doi><tpages>3</tpages></addata></record>
fulltext fulltext
identifier ISSN: 1439-7595
ispartof Modern rheumatology, 2014-07, Vol.24 (4), p.685-687
issn 1439-7595
1439-7609
language eng
recordid cdi_proquest_miscellaneous_1542299276
source MEDLINE; Oxford University Press Journals All Titles (1996-Current)
subjects Adult
Antibodies, Monoclonal, Murine-Derived - therapeutic use
Autoimmune diseases
Churg-Strauss Syndrome - drug therapy
Cyclophosphamide - therapeutic use
Drug therapy
Female
Glucocorticoids - therapeutic use
Humans
Immunoglobulins, Intravenous - therapeutic use
Immunologic Factors - therapeutic use
Prescription drugs
Retreatment
Rituximab
Treatment Outcome
title Successful treatment of eosinophilic granulomatosis with polyangiitis (EGPA; formerly Churg–Strauss syndrome) with rituximab in a case refractory to glucocorticoids, cyclophosphamide, and IVIG
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-14T18%3A51%3A32IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Successful%20treatment%20of%20eosinophilic%20granulomatosis%20with%20polyangiitis%20(EGPA;%20formerly%20Churg%E2%80%93Strauss%20syndrome)%20with%20rituximab%20in%20a%20case%20refractory%20to%20glucocorticoids,%20cyclophosphamide,%20and%20IVIG&rft.jtitle=Modern%20rheumatology&rft.au=Umezawa,%20Natsuka&rft.date=2014-07-01&rft.volume=24&rft.issue=4&rft.spage=685&rft.epage=687&rft.pages=685-687&rft.issn=1439-7595&rft.eissn=1439-7609&rft_id=info:doi/10.3109/14397595.2013.874734&rft_dat=%3Cproquest_cross%3E1542299276%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1544396305&rft_id=info:pmid/24517553&rfr_iscdi=true