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      "titulo" => "Tumor carcinóide do timo – Caso clínico"
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        "resumen" => "<p id="spar0005" class="elsevierStyleSimplePara elsevierViewall">A linfangioleiomiomatose &#40;LAM&#41; &#233; uma doen&#231;a rara&#44; de etiologia desconhecida&#44; caracterizada pela prolifera&#231;&#227;o anormal de c&#233;lulas musculares lisas nas regi&#245;es perilinf&#225;tica&#44; perivascular e peribr&#244;nquica&#46;</p><p id="spar0010" class="elsevierStyleSimplePara elsevierViewall">A LAM pode ocorrer esporadicamente ou associada ao complexo esclerose tuberosa &#40;CET&#41; e hamartose heredit&#225;ria multiorg&#226;nica<span class="elsevierStyleSup">1</span>&#46;</p><p id="spar0015" class="elsevierStyleSimplePara elsevierViewall">Em ambas as situa&#231;&#245;es a LAM afecta principalmente mulheres jovens em idade f&#233;rtil&#44; sendo que aproximadamente 1&#47;3 das mulheres com CET t&#234;m LAM<span class="elsevierStyleSup">2</span>&#46;</p><p id="spar0020" class="elsevierStyleSimplePara elsevierViewall">A prop&#243;sito desta patologia&#44; os autores elaboram uma revis&#227;o da literatura e descrevem os casos cl&#237;nicos de tr&#234;s doentes do sexo feminino com o diagn&#243;stico de LAM com base nos achados cl&#237;nicos e imagiol&#243;gicos&#46;</p>"
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