<?xml version="1.0" encoding="ISO-8859-1"?><article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
<front>
<journal-meta>
<journal-id>2184-0628</journal-id>
<journal-title><![CDATA[Gazeta Médica]]></journal-title>
<abbrev-journal-title><![CDATA[Gaz Med]]></abbrev-journal-title>
<issn>2184-0628</issn>
<publisher>
<publisher-name><![CDATA[Círculo Médico]]></publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id>S2184-06282021000300218</article-id>
<article-id pub-id-type="doi">10.29315/gm.v1i1.487</article-id>
<title-group>
<article-title xml:lang="en"><![CDATA[Terminal Ileitis: A Rare Complication of Henoch-Schönlein Purpura in Children]]></article-title>
<article-title xml:lang="pt"><![CDATA[Ileíte Terminal: Uma Complicação Rara da Púrpura de Henoch-Schönlein na Criança]]></article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Mano]]></surname>
<given-names><![CDATA[Ana Lia Costa]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Santos]]></surname>
<given-names><![CDATA[Mafalda Casinhas]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Limão]]></surname>
<given-names><![CDATA[Sara]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Cunha]]></surname>
<given-names><![CDATA[Florbela]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
</contrib-group>
<aff id="Af1">
<institution><![CDATA[,Centro Hospitalar Universitário de Lisboa Central Hospital Dona Estefânia ]]></institution>
<addr-line><![CDATA[Lisboa ]]></addr-line>
<country>Portugal</country>
</aff>
<aff id="Af2">
<institution><![CDATA[,Hospital Vila Franca de Xira Serviço de Pediatria ]]></institution>
<addr-line><![CDATA[Vila Franca de Xira ]]></addr-line>
<country>Portugal</country>
</aff>
<pub-date pub-type="pub">
<day>30</day>
<month>09</month>
<year>2021</year>
</pub-date>
<pub-date pub-type="epub">
<day>30</day>
<month>09</month>
<year>2021</year>
</pub-date>
<volume>8</volume>
<numero>3</numero>
<fpage>218</fpage>
<lpage>222</lpage>
<copyright-statement/>
<copyright-year/>
<self-uri xlink:href="http://scielo.pt/scielo.php?script=sci_arttext&amp;pid=S2184-06282021000300218&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://scielo.pt/scielo.php?script=sci_abstract&amp;pid=S2184-06282021000300218&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://scielo.pt/scielo.php?script=sci_pdf&amp;pid=S2184-06282021000300218&amp;lng=en&amp;nrm=iso"></self-uri><abstract abstract-type="short" xml:lang="en"><p><![CDATA[Abstract Henoch-Schönlein purpura (HSP) is characterized by nonthrombocytopenic palpable purpura, arthritis or arthralgia, and gastrointestinal and/or renal involvement. Gastrointestinal symptoms are reported in 50%-75% and they are related to a previous group A streptococcal infection in 40%. A healthy 5-year-old girl presented with a three-week history of a recurrent purpuric rash on the lower limbs, arthralgia and angioedema, without renal involvement. During the third relapse, she had severe, diffuse and persistent abdominal pain and bloody stools. An abdominal ultrasound revealed transmural edema of the last ileal segment, compatible with ileitis. She received prednisolone for five days, with full clinical recovery. Antistreptolysin O titer was elevated. The remaining laboratory tests were normal (antinuclear, anti-neutrophil and anti-Saccharomyces cerevisiae antibodies; rheumatoid factor; stool cultures, parasitological examination and viral antigen tests). One month later, an abdominal ultrasound revealed no abnormalities. Terminal ileitis is a very rare complication of HSP in children but has a good prognosis.]]></p></abstract>
<abstract abstract-type="short" xml:lang="pt"><p><![CDATA[Resumo A púrpura de Henoch-Schonlein (PHS) é caracterizada por púrpura palpável não trombocitopénica, artrite ou artralgia e envolvimento renal e/ou gastrointestinal. Os sintomas gastrointestinais ocorrem em 50%-75% dos casos e estão relacionados com infeção prévia a streptococus grupo A em 40%. Uma rapariga saudável com 5 anos de idade apresentou-se com história com 3 semanas de evolução de rash purpúrico recidivante nos membros inferiores, artralgia e angioedema, sem envolvimento renal. Durante a terceira recidiva, apresentou dor abdominal intensa, difusa e persistente e dejeções com sangue. A ecografia abdominal revelou edema transmural do último segmento ileal, compatível com ileíte. Cumpriu prednisolona por 5 dias, com recuperação clínica completa. O título anti-estreptolisina O estava elevado. A restante avaliação laboratorial era normal (anticorpos antinuclear, anti-neutrófilos e anti-Saccharomyces cerevisiae, fator reumatoide, cultura das fezes e exame parasitológico e teste de antigénio viral). Um mês depois, a ecografia abdominal não revelou alterações. A ileíte terminal é uma complicação rara da PHS, mas apresenta um bom prognóstico.]]></p></abstract>
<kwd-group>
<kwd lng="en"><![CDATA[Child]]></kwd>
<kwd lng="en"><![CDATA[Ileitis]]></kwd>
<kwd lng="en"><![CDATA[Purpura, Schoenlein-Henoch]]></kwd>
<kwd lng="pt"><![CDATA[Criança]]></kwd>
<kwd lng="pt"><![CDATA[Ileíte]]></kwd>
<kwd lng="pt"><![CDATA[Púrpura Henoch-Schonlein]]></kwd>
</kwd-group>
</article-meta>
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