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<article xsi:noNamespaceSchemaLocation="http://jats.nlm.nih.gov/publishing/1.1/xsd/JATS-journalpublishing1-mathml3.xsd" dtd-version="1.1" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance"><front><journal-meta><journal-id journal-id-type="publisher-id">PAR</journal-id><journal-title-group><journal-title>Proceedings of Anticancer Research</journal-title></journal-title-group><issn>2208-3545</issn><eissn>2208-3553</eissn><publisher><publisher-name>Bio-Byword Scientific Publishing Pty. Ltd.</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.26689/par.v2i3.489</article-id><article-categories><subj-group subj-group-type="heading"><subject>Article</subject></subj-group></article-categories><title>Congenital cystic adenomatoid malformation of lung mimicking lung cancer: a case report</title><url>https://artdesignp.com/journal/PAR/2/3/10.26689/par.v2i3.489</url><author>ZhaoYing,ZhangYongxiang,QiLeng,LiZhenwu,PengPang,QiXiaoli</author><pub-date pub-type="publication-year"><year>2018</year></pub-date><volume>2</volume><issue>3</issue><history><date date-type="pub"><published-time>2018-12-12</published-time></date></history><abstract>Abstract: We report a case of a 66-year-old woman with congenital cystic adenomatoid malformation (CCAM) that presented as a thin walled cyst on radiological imaging and mimicked lung cancer. The right pulmonary wedge resection was performed via thoracoscopic surgery. Pathologic results proved CCAM which though, uncommon may be misdiagnosed in adults.</abstract><keywords/></article-meta></front><body/><back><ref-list><ref id="B1" content-type="article"><label>1</label><element-citation publication-type="journal"><p>REFERENCES</p><pub-id pub-id-type="doi"/></element-citation></ref><ref id="B2" content-type="article"><label>2</label><element-citation publication-type="journal"><p>Châ€™in KY, Tang MY. Congenital adenomatoid malformation of one lobe of a lung with general anasarca. Arch Pathol(Chic),1949, 48(3):221-229.</p><pub-id pub-id-type="doi"/></element-citation></ref><ref id="B3" content-type="article"><label>3</label><element-citation publication-type="journal"><p>Moerman P, Fryns JP, Vanderberghe K, Devlieger H, Lauweryns JM. Pathogenesis of congenital cystic adenomatoid malformation of the lung. Histopathology. 1992, 21:315â€“321.</p><pub-id pub-id-type="doi"/></element-citation></ref><ref id="B4" content-type="article"><label>4</label><element-citation publication-type="journal"><p>Laberge J,Flageole H,Pugash D,et al.Outcome of the prenatally diagnosed congenital cystic adenomatoid lung malformation: a Canadian experience[J].Fetal Diagn Ther,2001,16(3):178-186.</p><pub-id pub-id-type="doi"/></element-citation></ref><ref id="B5" content-type="article"><label>5</label><element-citation publication-type="journal"><p>Khan N,Jones M,Greaves M. Congenital cystic adenomatoid malformation of an entire lung in a 33-year-old man: a case report and review of the literature[J].Br J Radiol, 2008, 81(971):276-278.</p><pub-id pub-id-type="doi"/></element-citation></ref><ref id="B6" content-type="article"><label>6</label><element-citation publication-type="journal"><p>Pelizzo G, Barbi E, Cordrich D, et al. Chronic inflammation in congenital cystic adenomatoid malformations. An underestimated risk factor? [J]. J Pediatr Surg, 2009, 44(3):616-619.</p><pub-id pub-id-type="doi"/></element-citation></ref><ref id="B7" content-type="article"><label>7</label><element-citation publication-type="journal"><p>Peranteau WH,Merchant AM,Hedrick HL,et al.Prenatal course and postnatal management of peripheral bronchial atresiaï¼šassociation with congenital cystic adenomatoid malâ€ formation of the lung[J]. Fetal Diagn Ther, 2008, 24(3):190-196.</p><pub-id pub-id-type="doi"/></element-citation></ref><ref id="B8" content-type="article"><label>8</label><element-citation publication-type="journal"><p>Stocker JT, Madewell JE, Drake RM. Congenital cystic adenomatoid malformation of the lung. Classification and morphologic spectrum. Hum Pathol, 1977, 8(2):155-171.</p><pub-id pub-id-type="doi"/></element-citation></ref><ref id="B9" content-type="article"><label>9</label><element-citation publication-type="journal"><p>MacSweeney F, Papagiannopoulos K, Goldstraw P, Sheppard MN, Corrin B, Nicholson AG. An assessment of the expanded classification of congenital cystic adenomatoid malformations and their relationship to malignant transformation. Am J Surg Path 2003, 27:1139 â€“ 1146.</p><pub-id pub-id-type="doi"/></element-citation></ref><ref id="B10" content-type="article"><label>10</label><element-citation publication-type="journal"><p>Muller CO, Berrebi D, Kheniche A, et al. Is radical lobectomy required in congenital cystic adenomatoid malformation? [J]. J Pediatr Surg, 2009,44(3):616-619.</p><pub-id pub-id-type="doi"/></element-citation></ref><ref id="B11" content-type="article"><label>11</label><element-citation publication-type="journal"><p>Lan CC, Wu HC, Lee CH, et al. Lung cancer with unusual presentation as a thin-walled cyst in a young nonsmoker[J]. J Thorac Oncol, 2010,5(9):1481-1482.</p><pub-id pub-id-type="doi"/></element-citation></ref><ref id="B12" content-type="article"><label>12</label><element-citation publication-type="journal"><p>Xue X, Wang P, Xue Q, et al. Comparative study of solitary thin-walled cavity lung cancer with computed tomography and pathological findings[J]. Lung Cancer,2012,78(1):45-50.</p><pub-id pub-id-type="doi"/></element-citation></ref><ref id="B13" content-type="article"><label>13</label><element-citation publication-type="journal"><p>Qi Y, Zhang Q, Huang Y, et al. Manifestations and pathological features of solitary thin walled cavity lung cancer observed by CT and PET/CT imaging[J]. Oncology Letters,2014,8(1):285-290.</p><pub-id pub-id-type="doi"/></element-citation></ref><ref id="B14" content-type="article"><label>14</label><element-citation publication-type="journal"><p>Farooqi AO, Cham M, Zhang L, et al. Lung cancer associated with cystic airspaces[J]. AJR,2012,199(4):781-786.</p><pub-id pub-id-type="doi"/></element-citation></ref><ref id="B15" content-type="article"><label>15</label><element-citation publication-type="journal"><p>Yamada S, Noguchi H, Nabeshima A, et al. Basaloid carcinoma of the lung associated with central cavitation: a unique surgical case focusing on cytological and immunohistochemical findings[J]. Diagnostic pathology,2012,7(1):175-180.</p><pub-id pub-id-type="doi"/></element-citation></ref></ref-list></back></article>
