Intravenous immunoglobulins for steroid‐refractory esophageal involvement related to polymyositis and dermatomyositis: A series of 73 patients

Objective To assess the long‐term outcome of esophageal complications in the group of patients receiving intravenous immunoglobulins (IVIG) for the treatment of severe steroid‐refractory esophageal involvement related to polymyositis/dermatomyositis (PM/DM). Methods We retrospectively reviewed the m...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Arthritis care & research (2010) 2010-12, Vol.62 (12), p.1748-1755
Hauptverfasser: Marie, I., Menard, J.‐F., Hatron, P. Y., Hachulla, E., Mouthon, L., Tiev, K., Ducrotte, P., Cherin, P.
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 1755
container_issue 12
container_start_page 1748
container_title Arthritis care & research (2010)
container_volume 62
creator Marie, I.
Menard, J.‐F.
Hatron, P. Y.
Hachulla, E.
Mouthon, L.
Tiev, K.
Ducrotte, P.
Cherin, P.
description Objective To assess the long‐term outcome of esophageal complications in the group of patients receiving intravenous immunoglobulins (IVIG) for the treatment of severe steroid‐refractory esophageal involvement related to polymyositis/dermatomyositis (PM/DM). Methods We retrospectively reviewed the medical records of 73 patients (39 with PM, 34 with DM) with steroid‐resistant esophageal involvement. Esophageal involvement was evaluated by clinical and manometric investigations. Results Seventy‐three patients with steroid‐refractory esophageal involvement related to PM/DM received IVIG therapy (2 gm/kg monthly). The median interval between PM/DM diagnosis and the onset of esophageal complications was 6 months. The most common clinical manifestations revealing esophageal dysfunction were dysphagia (69.9%), coughing while eating (61.6%), and gastroesophageal reflux into the pharynx and/or mouth (34.2%). Twenty‐five patients exhibited life‐threatening esophageal complications requiring exclusive enteral feeding; 33 patients (45.2%) with esophageal impairment developed aspiration pneumonia. Sixty patients (82.2%) exhibited resolution of esophageal clinical manifestations, leading to a return to normal oral feeding and ablation of feeding enteral tubes. Four other patients (5.5%) improved, although they still experienced mild dysphagia intermittently. Because of impaired cricopharyngeal muscle relaxation, another patient successfully underwent cricopharyngeal myotomy. Eight patients died from aspiration pneumonia (n = 6) and cancer (n = 2). Muscle weakness, thoracic myopathy, and aspiration pneumonia were independent predictive factors of IVIG‐treated esophageal complications in PM/DM patients. Conclusion Our findings indicate that IVIG should be considered in life‐threatening esophageal impairment complicating steroid‐resistant PM/DM. We also suggest that combined therapy of IVIG and high‐dose steroids may be the first‐line therapy in PM/DM patients with life‐threatening esophageal manifestations.
doi_str_mv 10.1002/acr.20325
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_815556586</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>1093461773</sourcerecordid><originalsourceid>FETCH-LOGICAL-c4585-6815fe6b37cc0512ff20cb6b019b17640014b26045c7131d0017c4dd160c67013</originalsourceid><addsrcrecordid>eNp9kc1O3DAURq2qVUHAoi9QeUe7GPC_M92NRqVFQkKqqNRd5Dg3YOTEwXYGZccj8Iw8CYYBdvRufK91dBbfh9AXSo4oIezY2HjECGfyA9plVNKFULL6-LaLfzvoIKVrUoazquLLz2iHEc0YEXoX3Z8OOZoNDGFK2PX9NIRLH5rJuyHhLkScMsTg2oe7-whdNDaHOGNIYbwyl2A8dsMm-A30MGQcwZsMLc4Bj8HP_RySyy5hM7S4hdibHF7_fuAVThAdJBw6rDkeTXbFkfbRp874BAcv7x76e_LzYv17cXb-63S9OltYISu5UBWVHaiGa2uJpKzrGLGNaghdNlQrQQgVDVNESKspp225tRVtSxWxShPK99Dh1jvGcDNBynXvkgXvzQAli7r4pSxJqkJ--y9JyZILRbXmBf2-RW0MKZXA6jG63sS5QPVTW3Vpq35uq7BfX7RT00P7Rr52U4DjLXDrPMzvm-rV-s9W-Qgce6FO</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1093461773</pqid></control><display><type>article</type><title>Intravenous immunoglobulins for steroid‐refractory esophageal involvement related to polymyositis and dermatomyositis: A series of 73 patients</title><source>MEDLINE</source><source>Wiley Online Library Journals Frontfile Complete</source><creator>Marie, I. ; Menard, J.‐F. ; Hatron, P. Y. ; Hachulla, E. ; Mouthon, L. ; Tiev, K. ; Ducrotte, P. ; Cherin, P.</creator><creatorcontrib>Marie, I. ; Menard, J.‐F. ; Hatron, P. Y. ; Hachulla, E. ; Mouthon, L. ; Tiev, K. ; Ducrotte, P. ; Cherin, P.</creatorcontrib><description>Objective To assess the long‐term outcome of esophageal complications in the group of patients receiving intravenous immunoglobulins (IVIG) for the treatment of severe steroid‐refractory esophageal involvement related to polymyositis/dermatomyositis (PM/DM). Methods We retrospectively reviewed the medical records of 73 patients (39 with PM, 34 with DM) with steroid‐resistant esophageal involvement. Esophageal involvement was evaluated by clinical and manometric investigations. Results Seventy‐three patients with steroid‐refractory esophageal involvement related to PM/DM received IVIG therapy (2 gm/kg monthly). The median interval between PM/DM diagnosis and the onset of esophageal complications was 6 months. The most common clinical manifestations revealing esophageal dysfunction were dysphagia (69.9%), coughing while eating (61.6%), and gastroesophageal reflux into the pharynx and/or mouth (34.2%). Twenty‐five patients exhibited life‐threatening esophageal complications requiring exclusive enteral feeding; 33 patients (45.2%) with esophageal impairment developed aspiration pneumonia. Sixty patients (82.2%) exhibited resolution of esophageal clinical manifestations, leading to a return to normal oral feeding and ablation of feeding enteral tubes. Four other patients (5.5%) improved, although they still experienced mild dysphagia intermittently. Because of impaired cricopharyngeal muscle relaxation, another patient successfully underwent cricopharyngeal myotomy. Eight patients died from aspiration pneumonia (n = 6) and cancer (n = 2). Muscle weakness, thoracic myopathy, and aspiration pneumonia were independent predictive factors of IVIG‐treated esophageal complications in PM/DM patients. Conclusion Our findings indicate that IVIG should be considered in life‐threatening esophageal impairment complicating steroid‐resistant PM/DM. We also suggest that combined therapy of IVIG and high‐dose steroids may be the first‐line therapy in PM/DM patients with life‐threatening esophageal manifestations.</description><identifier>ISSN: 2151-464X</identifier><identifier>ISSN: 2151-4658</identifier><identifier>EISSN: 2151-4658</identifier><identifier>DOI: 10.1002/acr.20325</identifier><identifier>PMID: 20722047</identifier><language>eng</language><publisher>Hoboken, USA: John Wiley &amp; Sons, Inc</publisher><subject>Adolescent ; Adult ; Aged ; Aged, 80 and over ; Cancer ; Dermatomyositis ; Dermatomyositis - complications ; Dermatomyositis - drug therapy ; Drug Tolerance ; Dysphagia ; Enteral feeding ; Esophageal Diseases - drug therapy ; Esophageal Diseases - epidemiology ; Esophageal Diseases - etiology ; Esophagus ; Female ; Follow-Up Studies ; Gastroesophageal reflux ; Glucocorticoids - pharmacology ; Humans ; Immunoglobulins ; Immunoglobulins, Intravenous - administration &amp; dosage ; Immunoglobulins, Intravenous - therapeutic use ; Immunologic Factors - administration &amp; dosage ; Immunologic Factors - therapeutic use ; Intravenous administration ; Male ; medical records ; Middle Aged ; Mouth ; Muscle contraction ; Muscles ; Myopathy ; Pharynx ; Pneumonia ; Polymyositis ; Polymyositis - complications ; Polymyositis - drug therapy ; Prevalence ; Retrospective Studies ; Steroid hormones ; Thorax ; Treatment Outcome ; Young Adult</subject><ispartof>Arthritis care &amp; research (2010), 2010-12, Vol.62 (12), p.1748-1755</ispartof><rights>Copyright © 2010 by the American College of Rheumatology</rights><rights>Copyright © 2010 by the American College of Rheumatology.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4585-6815fe6b37cc0512ff20cb6b019b17640014b26045c7131d0017c4dd160c67013</citedby><cites>FETCH-LOGICAL-c4585-6815fe6b37cc0512ff20cb6b019b17640014b26045c7131d0017c4dd160c67013</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%2Facr.20325$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Facr.20325$$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/20722047$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Marie, I.</creatorcontrib><creatorcontrib>Menard, J.‐F.</creatorcontrib><creatorcontrib>Hatron, P. Y.</creatorcontrib><creatorcontrib>Hachulla, E.</creatorcontrib><creatorcontrib>Mouthon, L.</creatorcontrib><creatorcontrib>Tiev, K.</creatorcontrib><creatorcontrib>Ducrotte, P.</creatorcontrib><creatorcontrib>Cherin, P.</creatorcontrib><title>Intravenous immunoglobulins for steroid‐refractory esophageal involvement related to polymyositis and dermatomyositis: A series of 73 patients</title><title>Arthritis care &amp; research (2010)</title><addtitle>Arthritis Care Res (Hoboken)</addtitle><description>Objective To assess the long‐term outcome of esophageal complications in the group of patients receiving intravenous immunoglobulins (IVIG) for the treatment of severe steroid‐refractory esophageal involvement related to polymyositis/dermatomyositis (PM/DM). Methods We retrospectively reviewed the medical records of 73 patients (39 with PM, 34 with DM) with steroid‐resistant esophageal involvement. Esophageal involvement was evaluated by clinical and manometric investigations. Results Seventy‐three patients with steroid‐refractory esophageal involvement related to PM/DM received IVIG therapy (2 gm/kg monthly). The median interval between PM/DM diagnosis and the onset of esophageal complications was 6 months. The most common clinical manifestations revealing esophageal dysfunction were dysphagia (69.9%), coughing while eating (61.6%), and gastroesophageal reflux into the pharynx and/or mouth (34.2%). Twenty‐five patients exhibited life‐threatening esophageal complications requiring exclusive enteral feeding; 33 patients (45.2%) with esophageal impairment developed aspiration pneumonia. Sixty patients (82.2%) exhibited resolution of esophageal clinical manifestations, leading to a return to normal oral feeding and ablation of feeding enteral tubes. Four other patients (5.5%) improved, although they still experienced mild dysphagia intermittently. Because of impaired cricopharyngeal muscle relaxation, another patient successfully underwent cricopharyngeal myotomy. Eight patients died from aspiration pneumonia (n = 6) and cancer (n = 2). Muscle weakness, thoracic myopathy, and aspiration pneumonia were independent predictive factors of IVIG‐treated esophageal complications in PM/DM patients. Conclusion Our findings indicate that IVIG should be considered in life‐threatening esophageal impairment complicating steroid‐resistant PM/DM. We also suggest that combined therapy of IVIG and high‐dose steroids may be the first‐line therapy in PM/DM patients with life‐threatening esophageal manifestations.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Cancer</subject><subject>Dermatomyositis</subject><subject>Dermatomyositis - complications</subject><subject>Dermatomyositis - drug therapy</subject><subject>Drug Tolerance</subject><subject>Dysphagia</subject><subject>Enteral feeding</subject><subject>Esophageal Diseases - drug therapy</subject><subject>Esophageal Diseases - epidemiology</subject><subject>Esophageal Diseases - etiology</subject><subject>Esophagus</subject><subject>Female</subject><subject>Follow-Up Studies</subject><subject>Gastroesophageal reflux</subject><subject>Glucocorticoids - pharmacology</subject><subject>Humans</subject><subject>Immunoglobulins</subject><subject>Immunoglobulins, Intravenous - administration &amp; dosage</subject><subject>Immunoglobulins, Intravenous - therapeutic use</subject><subject>Immunologic Factors - administration &amp; dosage</subject><subject>Immunologic Factors - therapeutic use</subject><subject>Intravenous administration</subject><subject>Male</subject><subject>medical records</subject><subject>Middle Aged</subject><subject>Mouth</subject><subject>Muscle contraction</subject><subject>Muscles</subject><subject>Myopathy</subject><subject>Pharynx</subject><subject>Pneumonia</subject><subject>Polymyositis</subject><subject>Polymyositis - complications</subject><subject>Polymyositis - drug therapy</subject><subject>Prevalence</subject><subject>Retrospective Studies</subject><subject>Steroid hormones</subject><subject>Thorax</subject><subject>Treatment Outcome</subject><subject>Young Adult</subject><issn>2151-464X</issn><issn>2151-4658</issn><issn>2151-4658</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kc1O3DAURq2qVUHAoi9QeUe7GPC_M92NRqVFQkKqqNRd5Dg3YOTEwXYGZccj8Iw8CYYBdvRufK91dBbfh9AXSo4oIezY2HjECGfyA9plVNKFULL6-LaLfzvoIKVrUoazquLLz2iHEc0YEXoX3Z8OOZoNDGFK2PX9NIRLH5rJuyHhLkScMsTg2oe7-whdNDaHOGNIYbwyl2A8dsMm-A30MGQcwZsMLc4Bj8HP_RySyy5hM7S4hdibHF7_fuAVThAdJBw6rDkeTXbFkfbRp874BAcv7x76e_LzYv17cXb-63S9OltYISu5UBWVHaiGa2uJpKzrGLGNaghdNlQrQQgVDVNESKspp225tRVtSxWxShPK99Dh1jvGcDNBynXvkgXvzQAli7r4pSxJqkJ--y9JyZILRbXmBf2-RW0MKZXA6jG63sS5QPVTW3Vpq35uq7BfX7RT00P7Rr52U4DjLXDrPMzvm-rV-s9W-Qgce6FO</recordid><startdate>201012</startdate><enddate>201012</enddate><creator>Marie, I.</creator><creator>Menard, J.‐F.</creator><creator>Hatron, P. Y.</creator><creator>Hachulla, E.</creator><creator>Mouthon, L.</creator><creator>Tiev, K.</creator><creator>Ducrotte, P.</creator><creator>Cherin, P.</creator><general>John Wiley &amp; Sons, Inc</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>7T5</scope><scope>H94</scope><scope>7X8</scope></search><sort><creationdate>201012</creationdate><title>Intravenous immunoglobulins for steroid‐refractory esophageal involvement related to polymyositis and dermatomyositis: A series of 73 patients</title><author>Marie, I. ; Menard, J.‐F. ; Hatron, P. Y. ; Hachulla, E. ; Mouthon, L. ; Tiev, K. ; Ducrotte, P. ; Cherin, P.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4585-6815fe6b37cc0512ff20cb6b019b17640014b26045c7131d0017c4dd160c67013</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>Adolescent</topic><topic>Adult</topic><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Cancer</topic><topic>Dermatomyositis</topic><topic>Dermatomyositis - complications</topic><topic>Dermatomyositis - drug therapy</topic><topic>Drug Tolerance</topic><topic>Dysphagia</topic><topic>Enteral feeding</topic><topic>Esophageal Diseases - drug therapy</topic><topic>Esophageal Diseases - epidemiology</topic><topic>Esophageal Diseases - etiology</topic><topic>Esophagus</topic><topic>Female</topic><topic>Follow-Up Studies</topic><topic>Gastroesophageal reflux</topic><topic>Glucocorticoids - pharmacology</topic><topic>Humans</topic><topic>Immunoglobulins</topic><topic>Immunoglobulins, Intravenous - administration &amp; dosage</topic><topic>Immunoglobulins, Intravenous - therapeutic use</topic><topic>Immunologic Factors - administration &amp; dosage</topic><topic>Immunologic Factors - therapeutic use</topic><topic>Intravenous administration</topic><topic>Male</topic><topic>medical records</topic><topic>Middle Aged</topic><topic>Mouth</topic><topic>Muscle contraction</topic><topic>Muscles</topic><topic>Myopathy</topic><topic>Pharynx</topic><topic>Pneumonia</topic><topic>Polymyositis</topic><topic>Polymyositis - complications</topic><topic>Polymyositis - drug therapy</topic><topic>Prevalence</topic><topic>Retrospective Studies</topic><topic>Steroid hormones</topic><topic>Thorax</topic><topic>Treatment Outcome</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Marie, I.</creatorcontrib><creatorcontrib>Menard, J.‐F.</creatorcontrib><creatorcontrib>Hatron, P. Y.</creatorcontrib><creatorcontrib>Hachulla, E.</creatorcontrib><creatorcontrib>Mouthon, L.</creatorcontrib><creatorcontrib>Tiev, K.</creatorcontrib><creatorcontrib>Ducrotte, P.</creatorcontrib><creatorcontrib>Cherin, P.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Immunology Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Arthritis care &amp; research (2010)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Marie, I.</au><au>Menard, J.‐F.</au><au>Hatron, P. Y.</au><au>Hachulla, E.</au><au>Mouthon, L.</au><au>Tiev, K.</au><au>Ducrotte, P.</au><au>Cherin, P.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Intravenous immunoglobulins for steroid‐refractory esophageal involvement related to polymyositis and dermatomyositis: A series of 73 patients</atitle><jtitle>Arthritis care &amp; research (2010)</jtitle><addtitle>Arthritis Care Res (Hoboken)</addtitle><date>2010-12</date><risdate>2010</risdate><volume>62</volume><issue>12</issue><spage>1748</spage><epage>1755</epage><pages>1748-1755</pages><issn>2151-464X</issn><issn>2151-4658</issn><eissn>2151-4658</eissn><abstract>Objective To assess the long‐term outcome of esophageal complications in the group of patients receiving intravenous immunoglobulins (IVIG) for the treatment of severe steroid‐refractory esophageal involvement related to polymyositis/dermatomyositis (PM/DM). Methods We retrospectively reviewed the medical records of 73 patients (39 with PM, 34 with DM) with steroid‐resistant esophageal involvement. Esophageal involvement was evaluated by clinical and manometric investigations. Results Seventy‐three patients with steroid‐refractory esophageal involvement related to PM/DM received IVIG therapy (2 gm/kg monthly). The median interval between PM/DM diagnosis and the onset of esophageal complications was 6 months. The most common clinical manifestations revealing esophageal dysfunction were dysphagia (69.9%), coughing while eating (61.6%), and gastroesophageal reflux into the pharynx and/or mouth (34.2%). Twenty‐five patients exhibited life‐threatening esophageal complications requiring exclusive enteral feeding; 33 patients (45.2%) with esophageal impairment developed aspiration pneumonia. Sixty patients (82.2%) exhibited resolution of esophageal clinical manifestations, leading to a return to normal oral feeding and ablation of feeding enteral tubes. Four other patients (5.5%) improved, although they still experienced mild dysphagia intermittently. Because of impaired cricopharyngeal muscle relaxation, another patient successfully underwent cricopharyngeal myotomy. Eight patients died from aspiration pneumonia (n = 6) and cancer (n = 2). Muscle weakness, thoracic myopathy, and aspiration pneumonia were independent predictive factors of IVIG‐treated esophageal complications in PM/DM patients. Conclusion Our findings indicate that IVIG should be considered in life‐threatening esophageal impairment complicating steroid‐resistant PM/DM. We also suggest that combined therapy of IVIG and high‐dose steroids may be the first‐line therapy in PM/DM patients with life‐threatening esophageal manifestations.</abstract><cop>Hoboken, USA</cop><pub>John Wiley &amp; Sons, Inc</pub><pmid>20722047</pmid><doi>10.1002/acr.20325</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 2151-464X
ispartof Arthritis care & research (2010), 2010-12, Vol.62 (12), p.1748-1755
issn 2151-464X
2151-4658
2151-4658
language eng
recordid cdi_proquest_miscellaneous_815556586
source MEDLINE; Wiley Online Library Journals Frontfile Complete
subjects Adolescent
Adult
Aged
Aged, 80 and over
Cancer
Dermatomyositis
Dermatomyositis - complications
Dermatomyositis - drug therapy
Drug Tolerance
Dysphagia
Enteral feeding
Esophageal Diseases - drug therapy
Esophageal Diseases - epidemiology
Esophageal Diseases - etiology
Esophagus
Female
Follow-Up Studies
Gastroesophageal reflux
Glucocorticoids - pharmacology
Humans
Immunoglobulins
Immunoglobulins, Intravenous - administration & dosage
Immunoglobulins, Intravenous - therapeutic use
Immunologic Factors - administration & dosage
Immunologic Factors - therapeutic use
Intravenous administration
Male
medical records
Middle Aged
Mouth
Muscle contraction
Muscles
Myopathy
Pharynx
Pneumonia
Polymyositis
Polymyositis - complications
Polymyositis - drug therapy
Prevalence
Retrospective Studies
Steroid hormones
Thorax
Treatment Outcome
Young Adult
title Intravenous immunoglobulins for steroid‐refractory esophageal involvement related to polymyositis and dermatomyositis: A series of 73 patients
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-14T10%3A21%3A24IST&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=Intravenous%20immunoglobulins%20for%20steroid%E2%80%90refractory%20esophageal%20involvement%20related%20to%20polymyositis%20and%20dermatomyositis:%20A%20series%20of%2073%20patients&rft.jtitle=Arthritis%20care%20&%20research%20(2010)&rft.au=Marie,%20I.&rft.date=2010-12&rft.volume=62&rft.issue=12&rft.spage=1748&rft.epage=1755&rft.pages=1748-1755&rft.issn=2151-464X&rft.eissn=2151-4658&rft_id=info:doi/10.1002/acr.20325&rft_dat=%3Cproquest_cross%3E1093461773%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=1093461773&rft_id=info:pmid/20722047&rfr_iscdi=true