Sudden blindness in a child with Crohn's disease
Inflammatory bowel disease (IBD) is often associated with extraintestinal manifestations (EIMs) such as optic neuritis (ON), although this has been described in only a few adult patients so far, all of whom were affected with Crohn's disease (CD). Furthermore, ON and demyelinating diseases have been...
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Veröffentlicht in: | 世界胃肠病学杂志:英文版 2011, Vol.17 (38), p.4344-4346 |
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container_title | 世界胃肠病学杂志:英文版 |
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creator | Arrigo Vittorio Barabino Paolo Gandullia Angela Calvi Silvia Vignola Serena Arrigo Riccardo De Marco |
description | Inflammatory bowel disease (IBD) is often associated with extraintestinal manifestations (EIMs) such as optic neuritis (ON), although this has been described in only a few adult patients so far, all of whom were affected with Crohn's disease (CD). Furthermore, ON and demyelinating diseases have been demonstrated to be more frequent in IBD patients than in control populations. In our current case report, we describe a child with active CD who developed sudden blindness due to bilateral ON that was not related to any known cause, and that promptly responded to a high dose of steroids. Investigations and a clinical follow-up have so far ruled out the development of demyelinating diseases in this patient. To our knowledge, this is the first report of ON in a pediatric patient with CD. Possible explanations for this case include an episodic EIM of an active bowel disease, an associated autoimmune disorder such as a recurrent isolated ON, the first manifestation of mul- tiple sclerosis, or another demyelinating disease that could appear in a later follow-up. |
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Furthermore, ON and demyelinating diseases have been demonstrated to be more frequent in IBD patients than in control populations. In our current case report, we describe a child with active CD who developed sudden blindness due to bilateral ON that was not related to any known cause, and that promptly responded to a high dose of steroids. Investigations and a clinical follow-up have so far ruled out the development of demyelinating diseases in this patient. To our knowledge, this is the first report of ON in a pediatric patient with CD. Possible explanations for this case include an episodic EIM of an active bowel disease, an associated autoimmune disorder such as a recurrent isolated ON, the first manifestation of mul- tiple sclerosis, or another demyelinating disease that could appear in a later follow-up.</description><identifier>ISSN: 1007-9327</identifier><identifier>EISSN: 2219-2840</identifier><language>eng</language><subject>EIMS ; IBD ; 失明 ; 孩子 ; 神经炎 ; 肠道疾病 ; 自身免疫性疾病</subject><ispartof>世界胃肠病学杂志:英文版, 2011, Vol.17 (38), p.4344-4346</ispartof><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Uhttp://image.cqvip.com/vip1000/qk/84123X/84123X.jpg</thumbnail><link.rule.ids>314,780,784,4024</link.rule.ids></links><search><creatorcontrib>Arrigo Vittorio Barabino Paolo Gandullia Angela Calvi Silvia Vignola Serena Arrigo Riccardo De Marco</creatorcontrib><title>Sudden blindness in a child with Crohn's disease</title><title>世界胃肠病学杂志:英文版</title><addtitle>World Journal of Gastroenterology</addtitle><description>Inflammatory bowel disease (IBD) is often associated with extraintestinal manifestations (EIMs) such as optic neuritis (ON), although this has been described in only a few adult patients so far, all of whom were affected with Crohn's disease (CD). Furthermore, ON and demyelinating diseases have been demonstrated to be more frequent in IBD patients than in control populations. In our current case report, we describe a child with active CD who developed sudden blindness due to bilateral ON that was not related to any known cause, and that promptly responded to a high dose of steroids. Investigations and a clinical follow-up have so far ruled out the development of demyelinating diseases in this patient. To our knowledge, this is the first report of ON in a pediatric patient with CD. Possible explanations for this case include an episodic EIM of an active bowel disease, an associated autoimmune disorder such as a recurrent isolated ON, the first manifestation of mul- tiple sclerosis, or another demyelinating disease that could appear in a later follow-up.</description><subject>EIMS</subject><subject>IBD</subject><subject>失明</subject><subject>孩子</subject><subject>神经炎</subject><subject>肠道疾病</subject><subject>自身免疫性疾病</subject><issn>1007-9327</issn><issn>2219-2840</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><recordid>eNpjYuA0MjK01DWyMDFgYeA0NDAw17U0NjLnYOAqLs4yMDAyNjY14mQwCi5NSUnNU0jKycxLyUstLlbIzFNIVEjOyMxJUSjPLMlQcC7Kz8h7v6e9WCElszg1sTiVh4E1LTGnOJUXSnMzKLq5hjh76CZn5OelF2bmpccXFGXmJhZVxpsYGFqYmBpYGBOjBgAXyTSD</recordid><startdate>2011</startdate><enddate>2011</enddate><creator>Arrigo Vittorio Barabino Paolo Gandullia Angela Calvi Silvia Vignola Serena Arrigo Riccardo De Marco</creator><scope>2RA</scope><scope>92L</scope><scope>CQIGP</scope><scope>W91</scope><scope>~WA</scope></search><sort><creationdate>2011</creationdate><title>Sudden blindness in a child with Crohn's disease</title><author>Arrigo Vittorio Barabino Paolo Gandullia Angela Calvi Silvia Vignola Serena Arrigo Riccardo De Marco</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-chongqing_primary_401845083</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>EIMS</topic><topic>IBD</topic><topic>失明</topic><topic>孩子</topic><topic>神经炎</topic><topic>肠道疾病</topic><topic>自身免疫性疾病</topic><toplevel>online_resources</toplevel><creatorcontrib>Arrigo Vittorio Barabino Paolo Gandullia Angela Calvi Silvia Vignola Serena Arrigo Riccardo De Marco</creatorcontrib><collection>中文科技期刊数据库</collection><collection>中文科技期刊数据库-CALIS站点</collection><collection>中文科技期刊数据库-7.0平台</collection><collection>中文科技期刊数据库-医药卫生</collection><collection>中文科技期刊数据库- 镜像站点</collection><jtitle>世界胃肠病学杂志:英文版</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Arrigo Vittorio Barabino Paolo Gandullia Angela Calvi Silvia Vignola Serena Arrigo Riccardo De Marco</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Sudden blindness in a child with Crohn's disease</atitle><jtitle>世界胃肠病学杂志:英文版</jtitle><addtitle>World Journal of Gastroenterology</addtitle><date>2011</date><risdate>2011</risdate><volume>17</volume><issue>38</issue><spage>4344</spage><epage>4346</epage><pages>4344-4346</pages><issn>1007-9327</issn><eissn>2219-2840</eissn><abstract>Inflammatory bowel disease (IBD) is often associated with extraintestinal manifestations (EIMs) such as optic neuritis (ON), although this has been described in only a few adult patients so far, all of whom were affected with Crohn's disease (CD). Furthermore, ON and demyelinating diseases have been demonstrated to be more frequent in IBD patients than in control populations. In our current case report, we describe a child with active CD who developed sudden blindness due to bilateral ON that was not related to any known cause, and that promptly responded to a high dose of steroids. Investigations and a clinical follow-up have so far ruled out the development of demyelinating diseases in this patient. To our knowledge, this is the first report of ON in a pediatric patient with CD. Possible explanations for this case include an episodic EIM of an active bowel disease, an associated autoimmune disorder such as a recurrent isolated ON, the first manifestation of mul- tiple sclerosis, or another demyelinating disease that could appear in a later follow-up.</abstract></addata></record> |
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source | Baishideng "World Journal of" online journals; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; PubMed Central; Alma/SFX Local Collection |
subjects | EIMS IBD 失明 孩子 神经炎 肠道疾病 自身免疫性疾病 |
title | Sudden blindness in a child with Crohn's disease |
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