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Caso Clínico/Clinical Case
Carcinoma bronquíolo-alveolar associado a malformação congénita das vias aéreas pulmonares em adolescente assintomático
Bronchioloalveolar carcinoma associated with congenital pulmonary airway malformation in an asymptomatic adolescent
Francisco Abecasis1, Maria Gomes Ferreira2, Ana Oliveira3, Henrique Vaz Velho4
1 Interno do Internato Complementar de Pediatria, Hospital Garcia de Orta, Almada
2 Assistente Hospitalar Graduada de Pediatria, Hospital Garcia de Orta, Almada
3 Assistente Hospitalar Graduada de Anatomia Patológica do Hospital Garcia de Orta, Almada
4 Chefe do Serviço de Cirurgia Cardiotorácica do Hospital de Santa Marta
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        "resumen" => "<span id="as0005" class="elsevierStyleSection elsevierViewall"><p id="sp0005" class="elsevierStyleSimplePara elsevierViewall">A malforma&#231;&#227;o cong&#233;nita das vias a&#233;reas pulmonares &#40;CPAM&#41; &#233; uma entidade rara com potencial de transforma&#231;&#227;o maligna&#46; Relata-se o caso de um rapaz de 14 anos&#44; assintom&#225;tico&#44; referenciado &#224; consulta ap&#243;s detec&#231;&#227;o de imagem nodular na base do pulm&#227;o direito num radiograma de t&#243;rax&#46; A tomografia computorizada &#40;TC&#41; mostrou&#44; no pulm&#227;o direito&#44; forma&#231;&#227;o redonda de m&#233;dia densidade com centro cavitado&#46; Ap&#243;s um ano de seguimento&#44; mantinha-se assintom&#225;tico&#44; sendo a imagem radiol&#243;gica sobrepon&#237;vel&#46; Em conjunto com a equipa de cirurgia cardiotor&#225;cica foi decidido proceder a bi&#243;psia excisional&#46; O exame histol&#243;gico revelou um carcinoma bronqu&#237;olo-alveolar mucinoso associado a CPAM tipo 1&#46; Perante este resultado&#44; o doente foi submetido a lobectomia inferior direita&#46; No exame histol&#243;gico do restante lobo&#44; n&#227;o se identificou tumor ou malforma&#231;&#227;o residuais&#46; Mant&#233;m-se assintom&#225;tico e sem complica&#231;&#245;es passados dois anos&#46; Tanto quanto &#233; do conhecimento dos autores&#44; este &#233; o primeiro caso desta rara associa&#231;&#227;o em Portugal&#46; Discute-se a abordagem de les&#245;es qu&#237;sticas em doentes assintom&#225;ticos&#46;</p><p id="sp0010" class="elsevierStyleSimplePara elsevierViewall"><span class="elsevierStyleBold">Rev Port Pneumol 2007&#59; XIV &#40;2&#41;&#58; 285-290</span></p></span>"
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        "resumen" => "<span id="as0010" class="elsevierStyleSection elsevierViewall"><p id="sp0015" class="elsevierStyleSimplePara elsevierViewall">Congenital pulmonary airway malformation &#40;CPAM&#41; is a rare entity with potential for malignant transformation&#46; We describe the case of a fourteen-year-old boy evaluated for the presence of a nodular image on the right lung on the chest x-ray&#46; Computerized Tomography &#40;CT&#41; showed a round lesion of medium density with cavitation on the right lung&#46; After one year of follow-up the patient was still asymptomatic and the image was similar&#46; With the agreement of the cardiothoracic surgeons an excisional biopsy was performed&#46; The histological examination revealed a mucinous bronchioloalveolar carcinoma associated with a type 1 CPAM&#46; The patient was then submitted to right inferior lobectomy&#46; After two years follow-up he is asymptomatic and free of complications&#46; To the authors best knowledge this is the first case reported in Portugal of this rare association&#46; The approach to cystic lesions in asymptomatic patients is discussed&#46;</p><p id="sp0020" class="elsevierStyleSimplePara elsevierViewall"><span class="elsevierStyleBold">Rev Port Pneumol 2007&#59; XIV &#40;2&#41;&#58; 285-290</span></p></span>"
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Article information
ISSN: 08732159
Original language: Portuguese
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