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Artykuły w czasopismach na temat „Congenital cystic adenomatoid malformations”

Autor: Grafiati

Data publikacji: 3 czerwca 2025

Data aktualizacji: 31 lipca 2025

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1

Scamporlino, Adriana, Andrea Ambrosini, Ercole Turrini, Uliano Morandi, and Alessandro Stefani. "Congenital cystic adenomatoid malformation in adults, presenting as a single cyst." Asian Cardiovascular and Thoracic Annals 26, no. 5 (2018): 407–9. http://dx.doi.org/10.1177/0218492318776572.

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Congenital cystic adenomatoid malformations are lung anomalies usually detected prenatally or in newborns and infants. Type 1 congenital cystic adenomatoid malformations appears as a multicystic lesion, with cysts up to 2 cm in diameter, or as a single large cyst. In the latter case, when detected in adults, the preoperative diagnosis is challenging because congenital cystic adenomatoid malformations can be confused with other more common lesions. We describe two cases of uniloculated type 1 congenital cystic adenomatoid malformation in adults. In both cases, the preoperative clinical diagnosi

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2

Soomro, Shazia ,., Misbah Anjum, Shazia Kulsoom, Safia Bibi, Pervez Ali, and Bilquis Naeem. "Clinical Presentation and Outcome of Congenital Thoracic Malformations in Children Beyond Neonatal Period." Pakistan Journal of Medical and Health Sciences 16, no. 8 (2022): 775–77. http://dx.doi.org/10.53350/pjmhs22168775.

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Objective: To describe the clinical spectrum of presentation and outcome of children with congenital thoracic malformations beyond neonatal age. Methodology: Cross sectional study conducted at inpatient department of National institute of child health from Jan-Dec 2021. All patients hospitalized in study duration with diagnosis of congenital thoracic formations from 1 month till 12 years of age were enrolled. History, examination, laboratory tests, treatment and outcome were recorded. Results: Total 44 children were enrolled with mean age of 7.7+10.8 months. Common congenital thoracic malforma

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3

Ilina, N. A. "CT angiography as a main method of diagnostics of rear forms of congenital pulmonary malformations in newborns." Regional blood circulation and microcirculation 14, no. 2 (2015): 34–40. http://dx.doi.org/10.24884/1682-6655-2015-14-2-34-40.

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Relevance. Congenital pulmonary abnormalities are revealed considerably more often than it was supposed. In many children, they represent the main reason for development of inflammatory process or respiratory failure. The improvement of diagnostic methods resulted in the fact that congenital pulmonary malformations are diagnosed in children of early age and even in the neonatal period. For the correct choice of treatment tactics and timing in congenital pulmonary malformations in newborns, it is very important to differentiate among several types of malformations, including congenital cystic a

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4

Pratima, Jonnadula, K. Durga, and G. Bhavana. "Congenital Cystic Adenomatoid Malformation of Lung - Case Series." International Journal of Research and Review 10, no. 9 (2023): 84–88. http://dx.doi.org/10.52403/ijrr.20230910.

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Congenital cystic adenomatoid malformation (CCAM) is a rare entity with unexplained cause that effects the distal bronchi. It accounts for 25% of congenital pulmonary malformations with surgical excision as the treatment of choice. The mortality rate of patients with CCAM ranges from 9 to 49% if diagnosed prenatally. The outcome of a patient mainly depends on the presence of hydrops foetalis, microscopic type of CCAM, and the size of the lesions. The mainstay treatment of CCAM is surgical excision of the lesion which prevents complications of repeated infections, pneumothorax, and malignancy.

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5

Santosham, Rajan, Rajiv Santosham, Vamshidhar Tirunagari, and Sheba SK Jacob. "Adenocarcinoma in situ in type I congenital pulmonary airway malformation." Asian Cardiovascular and Thoracic Annals 27, no. 7 (2019): 606–8. http://dx.doi.org/10.1177/0218492319860346.

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Congenital pulmonary airway malformation, previously known as congenital cystic adenomatoid malformation, is a rare developmental anomaly of the lower respiratory tract. Widespread use of ultrasonography in the prenatal period has increased the rate of early diagnosis of congenital pulmonary airway malformations, thus adult presentation of this condition is extremely unusual. Adenocarcinoma in situ is seen very rarely in adolescent and adult patients with long-standing congenital pulmonary airway malformations. We describe a 28-year-old man with type I congenital pulmonary airway malformation

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6

Imai, Yukihiro, and Eugene J. Mark. "Cystic Adenomatoid Change Is Common to Various Forms of Cystic Lung Diseases of Children." Archives of Pathology & Laboratory Medicine 126, no. 8 (2002): 934–40. http://dx.doi.org/10.5858/2002-126-0934-cacict.

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Abstract Context.—Congenital cystic adenomatoid malformation, intralobar sequestration, extralobar sequestration, bronchopulmonary foregut malformation, bronchial atresia, and lobar emphysema generally are treated as separate entities, but there are commonalities among them. Objective.—To clarify the identity of congenital cystic adenomatoid malformation in relation to other cystic diseases. Design.—We studied 10 consecutive cases of surgically resected cystic lung disease in children. We studied the bronchial and vascular trees by mapping bronchi, pulmonary blood vessels, systemic blood vesse

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7

Mohammed, Salem, Al-Ahmadi Abdulaziz, Al-Ahmadi Basil, et al. "Hemoptysis in a Young Adult with Congenital Cystic Adenomatoid Malformation of the Lung: Case Report." International Journal of Medical and Pharmaceutical Case Reports 9, no. 2 (2017): 1–7. https://doi.org/10.9734/IJMPCR/2017/33875.

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Congenital cystic adenomatoid malformations (CCAM), also named congenital pulmonary airway malformation s (CPAM) are multicystic masses of segmental lung tissue with abnormal bronchial proliferation. There is failure of normal bronchoalveolar development with a hamartomatous proliferation of terminal respiratory units in a gland-like pattern (adenomatoid). CPAM can be divided into five types, according to clinical and pathologic features. [1] CPAM type 1 is the most common, and has good prognosis. The widespread use of antenatal ultrasound examination has resulted in an increase in the prenata

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8

Haryono, Dedy C., Muhammad Kartika, Prima K. Hayuningrat, and Darmawan Ismail. "Congenital cystic adenomatoid malformation: a rare serial case report." International Surgery Journal 9, no. 1 (2021): 190. http://dx.doi.org/10.18203/2349-2902.isj20215155.

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Congenital cystic adenomatoid malformation (CCAM) is a rare congenital lung malformation which a part of the lung becomes polycystic. CCAM accounts for 25% of congenital lung malformations and 95% of lung lesions. Case 1 was a 5-month-old female infant who was diagnosed with pneumothorax, with multiple cysts in the right lung, using chest computed tomography (CT). Thoracotomy lung resection was performed. Case 2 was one-day-old newborn infant who had respiratory distress with Downe score 3. Multiple cystic lesions with septations in left lung was observed on chest CT. Lobectomy inferior lobes

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9

Febriani, Andi Dwi Bahagia, Nurul Sylvana Shoraya, and Ema Alasiry. "Congenital Cystic Adenomatoid Malformations Type 1: Case Report." Open Access Macedonian Journal of Medical Sciences 10, no. C (2022): 123–25. http://dx.doi.org/10.3889/oamjms.2022.8539.

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BACKGROUND: Congenital cystic adenomatoid malformation (CCAM) is a group of multicystic and non-cystic masses due to abnormal lung development. The incidence ranges from 1: 10,000 to 1: 35,000 pregnancies. CASE REPORT: We report a case of a 3-day male baby presented with worsening respiratory distress, X-ray and chest CT were suggestive of CCAM, and sepsis. CONCLUSION: The current case adds to the collective clinical and radiological knowledge of this rare congenital lung disorder.

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10

Adama, Dembélé, Ouédraogo Issa, Kiemtoré Sibraogo Sibraogo, and Bambara Moussa. "Congenital cystic adenomatoid malformation, antenatal diagnosis: about one case." International Journal of Reproduction, Contraception, Obstetrics and Gynecology 8, no. 7 (2019): 2901. http://dx.doi.org/10.18203/2320-1770.ijrcog20193065.

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Antenatal ultrasound screening of fetal malformations requires for management, the immediate nature of which at certain birth, conditions the survival of the newborn. The Objectives Describe a case of pulmonary cystic adenomatoid malformation discover during antenatal ultrasonography. It was a 36 years old primary patient, referred to the maternity of Lafontaine hospital (France) for the presence, on obstetrical ultrasound screening, of suspected lesions on the foetal right lung’s field in a 21 weeks gestation pregnancy. After successive obstetric ultrasound scan, it was discovered that the le

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11

Mendeloff, Eric N. "Sequestrations, congenital cystic adenomatoid malformations, and congenital lobar emphysema." Seminars in Thoracic and Cardiovascular Surgery 16, no. 3 (2004): 209–14. http://dx.doi.org/10.1053/j.semtcvs.2004.08.007.

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12

Marshall, Kelley W., Caroline E. Blane, Daniel H. Teitelbaum, and Kathy van Leeuwen. "Congenital Cystic Adenomatoid Malformation." American Journal of Roentgenology 175, no. 6 (2000): 1551–54. http://dx.doi.org/10.2214/ajr.175.6.1751551.

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13

Moore, Lisa, and Rachel Handy. "Congenital Cystic Adenomatoid Malformation." Journal of Diagnostic Medical Sonography 25, no. 3 (2009): 168–72. http://dx.doi.org/10.1177/8756479309335683.

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14

Rosado-de-Christenson, M. L., and J. T. Stocker. "Congenital cystic adenomatoid malformation." RadioGraphics 11, no. 5 (1991): 865–86. http://dx.doi.org/10.1148/radiographics.11.5.1947321.

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15

Cloutier, Michelle M., David A. Schaeffer, and Donald Hight. "Congenital Cystic Adenomatoid Malformation." Chest 103, no. 3 (1993): 761–64. http://dx.doi.org/10.1378/chest.103.3.761.

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16

Alshamiri, Kamal M., and Hatem B. Abbod. "Congenital cystic adenomatoid malformation." International Journal of Pediatrics and Adolescent Medicine 4, no. 4 (2017): 159–60. http://dx.doi.org/10.1016/j.ijpam.2017.12.001.

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17

Norris, Mary. "Congenital cystic adenomatoid malformation." Australasian Journal of Ultrasound in Medicine 12, no. 3 (2009): 39–41. http://dx.doi.org/10.1002/j.2205-0140.2009.tb00059.x.

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18

Chauhan, VarshaH, AmarM Taksande, and KY Vilhekar. "Congenital Cystic Adenomatoid Malformation." Journal of the Pediatrics Association of India 1, no. 3 (2012): 123. http://dx.doi.org/10.4103/2667-3592.300347.

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19

Shukla, S., H. Kini, ML Ilias, and K. Gautam. "Hydrops fetalis secondary to supradiaphragmatic extrapulmonary sequestration with congenital cystic adenomatoid malformation." Journal of Pathology of Nepal 7, no. 1 (2017): 1130–32. http://dx.doi.org/10.3126/jpn.v7i1.16941.

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Congenital cystic adenomatoid malformation is a hamartomatous lesion. A 30 year old woman, G2P1L1, in the 29th week of gestation presented with pain abdomen, chest pain, cough with expectoration, fever and inability to appreciate fetal movements of 2 days duration. Clinically, she had pneumonia. An ultrasound revealed a single fetus in breech presentation with features of hydrops fetalis, hypoplastic left lung, mediastinal shift to the left and poor diastolic and systolic flow in the umbilical artery.A still born male baby delivered subsequently was found at autopsy to have hydrops fetalis, su

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20

Dauge, Coralie, Tanguy Fenouil, Thierry Petit, Corinne Jeanne-Pasquier, and Sophie Collardeau-Frachon. "Pulmonary Infantile Hemangioma Mimicking a Congenital Cystic Adenomatoid Malformation." Pediatric and Developmental Pathology 22, no. 5 (2019): 480–85. http://dx.doi.org/10.1177/1093526619838743.

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Infantile hemangioma (IH) is the most common benign vascular tumor of infancy, occurring predominantly in the head and neck. It is characterized by specific endothelial expression of glucose transporter-1 (GLUT-1) and involution with time, spontaneous or on beta-blockers treatment. Although some predisposing factors are known, the exact pathogenesis remains unclear. We report a case of pulmonary IH GLUT-1 positive, initially suspected as a cystic pulmonary airway malformation, in a child presenting with both cardiac and renal malformations. The clinical, radiological, pathological, and genetic

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21

Butterworth, Sonia A., and Geoffrey K. Blair. "Postnatal spontaneous resolution of congenital cystic adenomatoid malformations." Journal of Pediatric Surgery 40, no. 5 (2005): 832–34. http://dx.doi.org/10.1016/j.jpedsurg.2005.01.051.

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22

Curran, Patrick F., Eric B. Jelin, Larry Rand, et al. "Prenatal steroids for microcystic congenital cystic adenomatoid malformations." Journal of Pediatric Surgery 45, no. 1 (2010): 145–50. http://dx.doi.org/10.1016/j.jpedsurg.2009.10.025.

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23

Bajpai, Jyoti, Shreya Verma, Surya Kant, et al. "Hybrid Pulmonary Sequestration, Cystic Pulmonary Adenomatoid Malformation, and Dextrocardia: A Triple Whammy." International Journal of Applied & Basic Medical Research 14, no. 1 (2024): 67–69. http://dx.doi.org/10.4103/ijabmr.ijabmr_376_23.

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Abstract Pulmonary sequestration and cystic pulmonary adenomatoid malformation are rare congenital cystic disorders of the lungs. The presence of both the diseases in the same individual is therefore very uncommon. Pulmonary sequestration is a nonfunctional pulmonary tissue mass that derives its blood supply from systemic blood supply other than pulmonary circulation. Congenital cystic pulmonary adenomatoid malformation represents a mass consisting of abnormal bronchiolar air spaces and a deficiency of functional alveoli. This is the case report of a 9-year-old girl with intermittent fever, le

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24

Iftikhar Ahmed, Chaudhry, Khan Mohammad Nasim, Alqahtani Yousif A, et al. "Pulmonary congenital cystic adenomatoid malformation: a rare congenital abnormality in adults and review of literature." Journal of Pulmonology and Respiratory Research 6, no. 2 (2022): 016–19. http://dx.doi.org/10.29328/journal.jprr.1001038.

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Congenital cystic adenomatoid malformation of the lung (CCAM) is characterized by an adenomatoid proliferation of bronchiole-like structures and cysts formation. The condition is most commonly found in newborns and children and may be associated with other malformations; rarely, the presentation is delayed until adulthood. We herein report two cases of CCAM in adult patients. 22 years old healthy female with pre-employment health screening chest X-ray showed a lesion in the upper lobe of the right lung. In another case, a computed tomographic scan of the thorax (CT) confirmed a mass in the upp

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25

Chuang, Ming-Tsung, Twei-Shiun Jaw, Heong-Ieng Wong, Chia-Ying Lu, and Jui-Sheng Hsu. "Bilateral Congenital Cystic Adenomatoid Malformation." Annals of Thoracic Surgery 83, no. 1 (2007): e2. http://dx.doi.org/10.1016/j.athoracsur.2006.09.074.

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Breytenbach, Margaretha. "Fetal congenital cystic adenomatoid malformation." Sonography 2, no. 2 (2015): 43–48. http://dx.doi.org/10.1002/sono.12027.

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ÖZDEMİR, Özmert M. A., Hacer ERGİN, Abdullah KARACA, Uğur KOLTUKSUZ, Nevzat KARABULUT, and Nagihan YALÇIN. "Congenital Cystic Adenomatoid Malformation: Case Report." Turkiye Klinikleri Journal of Medical Sciences 30, no. 2 (2010): 798–802. http://dx.doi.org/10.5336/medsci.2008-7564.

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Jaffe, A., and L. S. Chitty. "Congenital cystic adenomatoid malformations may not require surgical intervention." Archives of Disease in Childhood - Fetal and Neonatal Edition 91, no. 6 (2006): F464. http://dx.doi.org/10.1136/adc.2006.093716.

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Raychaudhuri, P., A. Pasupati, A. James, B. Whitehead, and R. Kumar. "Prospective study of antenatally diagnosed congenital cystic adenomatoid malformations." Pediatric Surgery International 27, no. 11 (2011): 1159–64. http://dx.doi.org/10.1007/s00383-011-2909-1.

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Ierullo, A. M., R. Ganapathy, S. Crowley, L. Craxford, A. Bhide, and B. Thilaganathan. "Neonatal outcome of antenatally diagnosed congenital cystic adenomatoid malformations." Ultrasound in Obstetrics and Gynecology 26, no. 2 (2005): 150–53. http://dx.doi.org/10.1002/uog.1920.

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Lau, Chin-Tung, and Kenneth K. Y. Wong. "Thoracoscopic Resection of Congenital Cystic Adenomatoid Malformation in a Patient with Fused Lung Fissure Using Hookwire." Innovations: Technology and Techniques in Cardiothoracic and Vascular Surgery 13, no. 3 (2018): 226–29. http://dx.doi.org/10.1097/imi.0000000000000501.

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Thoracoscopic resection is being used more commonly for the treatment of congenital cystic adenomatoid malformation in neonates and infants. However, in the rare case of congenital cystic adenomatoid malformation with congenital absence of lung fissure, thoracoscopic lobectomy cannot be performed safely. Moreover, if the lung lesion is deep-seated and cannot be visualized on the pleural surface, wedge resection may result in residual lesion. Here, we reported our approach of thoracoscopic resection under hookwire guidance to tackle this problem.

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32

Karim, Meskouri. "Surgical Approach to Pulmonary Cystic Adenomatoid Malformations: About an Observation." Greenfort International Journal of Applied Medical Science 2, no. 2 (2024): 47–52. http://dx.doi.org/10.62046/gijams.2024.v02i02.004.

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Congenital cystic adenomatoid malformation (MAKC) is a congenital anomaly of lung development, and is defined as an adenomatoid proliferation of terminal respiratory structures, bronchial and distal pulmonary cystic dilatation, communicating with the bronchial tree and lacking cartilaginous rings, representing approximately 25% of congenital lung lesions, and in 80 to 85% of cases, the diagnosis is made before the age of 2 and is rarely discovered in adulthood. We report 01 case of MAKC diagnosed at the age of 06 months. The diagnosis was based on clinical elements (episode of bronchiolitis wi

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33

Bolano Charris, Veronica, Angie Gomez Arias, Andres Todaro, et al. "Congenital Cystic Adenomatoid Malformation in a Premature Newborn: Case Report." International Journal of Science and Research (IJSR) 13, no. 10 (2024): 842–45. http://dx.doi.org/10.21275/sr241011183658.

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Reis, Alice Rebelo de Matos Borges dos, Frederico Becker Ribeiro, and Regina Schultz. "Congenital cystic adenomatoid malformation type I." Autopsy and Case Reports 5, no. 3 (2015): 21–26. http://dx.doi.org/10.4322/acr.2015.019.

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Yamasue, Mari, Shin-ichi Nureki, Michiyo Miyawaki, and Jun-ichi Kadota. "Congenital Cystic Adenomatoid Malformation in Adults." Internal Medicine 54, no. 23 (2015): 3097–98. http://dx.doi.org/10.2169/internalmedicine.54.5512.

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Markhardt, B. Keegan, Diana L. Farmer, and Roy A. Filly. "Presumptive Intrahepatic Congenital Cystic Adenomatoid Malformation." Journal of Ultrasound in Medicine 22, no. 5 (2003): 531–36. http://dx.doi.org/10.7863/jum.2003.22.5.531.

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Patz, Edward F., Nestor L. Müller, Stephen J. Swensen, and Leslie G. Dodd. "Congenital Cystic Adenomatoid Malformation in Adults." Journal of Computer Assisted Tomography 19, no. 3 (1995): 361–64. http://dx.doi.org/10.1097/00004728-199505000-00004.

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Sahu, S., S. Muthuvel, SS Naware, and SS Dhavala. "Congenital Cystic Adenomatoid Malformation of Lung." Medical Journal Armed Forces India 64, no. 3 (2008): 268–69. http://dx.doi.org/10.1016/s0377-1237(08)80113-x.

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van Koningsbruggen, Silke, F. Ahrens, M. Brockmann, D. Michalk, and E. Rietschel. "Congenital cystic adenomatoid malformation type 4." Pediatric Pulmonology 32, no. 6 (2001): 471–75. http://dx.doi.org/10.1002/ppul.1160.

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Patil, Nanda, Vaidehi Nagar, and Chirag Sharma. "Exencephaly with Cystic Adenomatoid Malformation- A Review of a Rare Case." Galore International Journal of Health Sciences and Research 6, no. 2 (2021): 45–47. http://dx.doi.org/10.52403/gijhsr.20210406.

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Exencephaly is a rare malformation of the cranium which is characterized by absence of skull, cranium cavity and a scalp with protruding brain tissue outside the skull. The prognosis for infants born with this malformation is extremely poor. Exencephaly has been associated with several other congenital anomalies. We present a case of exencephaly associated with cystic adenomatoid malformation in autopsy findings in a17weeks female abortus. Keywords: Exencephaly, acrania, cystic adenomatoid malformation.

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Mosawi, Aamir. "The First of Congenital Cystic Adenomatoid Lung Malformation in Iraq: A Radiologic and Pathologic Study." Clinical Research Notes 1, no. 1 (2020): 01–03. http://dx.doi.org/10.31579/2690-8816/005.

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Background: Congenital cystic adenomatoid lung malformation is a very rare condition characterized by replacement of normal pulmonary tissue with cysts of variable size and distribution. The condition is usually unilateral. Very few cases of bilateral and congenital cystic adenomatoid malformation with good outcome after resections of the lesions have been reported, and most cases were stillborn or died early during life. Patients and methods: A forty-day male infant presented with progressive respiratory distress since the first week of life observed at the Children Teaching Hospital of Baghd

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Nam, So Hyun, Min Jeong Cho, and Dae Yeon Kim. "Minimally invasive surgery for congenital cystic adenomatoid malformations - early experience." Annals of Surgical Treatment and Research 90, no. 2 (2016): 101. http://dx.doi.org/10.4174/astr.2016.90.2.101.

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Erginel, Başak. "Pulmonary sublobar resections in children with congenital cystic adenomatoid malformations." Turkish Journal of Thoracic and Cardiovascular Surgery 23, no. 4 (2015): 695–99. http://dx.doi.org/10.5606/tgkdc.dergisi.2015.10500.

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Chen, Wei-Shiu, Guang-Perng Yeh, Horng-Der Tsai, and Charles Tsung-Che Hsieh. "Prenatal Diagnosis of Congenital Cystic Adenomatoid Malformations: Evolution and Outcome." Taiwanese Journal of Obstetrics and Gynecology 48, no. 3 (2009): 278–81. http://dx.doi.org/10.1016/s1028-4559(09)60304-1.

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Sobh, Eman, Amira Bahour, and Shady Elia Anis. "It is not pneumothorax: Multicystic lung lesion in a six-year-old child." Proceedings of Singapore Healthcare 26, no. 2 (2016): 121–24. http://dx.doi.org/10.1177/2010105816664357.

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Congenital cystic adenomatoid malformation (CCAM) – recently reported as congenital pulmonary airway malformation – is a rare abnormality of lung development. We present a case of a six-year-old child having a cystic lung lesion that proved to be CCAM after surgical resection. The child is performing well on follow-up.

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CHUANG, SANDRA, ELLA SUGO, and ADAM JAFFE. "A REVIEW OF POSTNATAL MANAGEMENT OF CONGENITAL PULMONARY AIRWAY MALFORMATIONS." Fetal and Maternal Medicine Review 20, no. 3 (2009): 179–204. http://dx.doi.org/10.1017/s0965539509990052.

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Congenital cystic adenomatoid malformations of the lung (CCAMs) were originally described by Ch'In and Tang in 1949 as rare lung lesions occurring in premature or stillborn infants with anasarca. In 1977 Stocker et al divided CCAM into three types based on their clinical and pathological features. The nomenclature has since changed to congenital pulmonary airway malformations (CPAMs) to reflect the possible absence of cystic changes and the probable underlying pathogenesis of different types. CPAMs are relatively rare congenital abnormalities with a reported incidence varying from 1 in 10,000

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Malinova, Doroteya V., Penka L. Kolova, and Radoslav S. Radev. "Congenital Cystic Adenomatoid Malformation Of The Lung: A Case Report And Review Of The Literature." Journal of Biomedical and Clinical Research 8, no. 2 (2015): 160–63. http://dx.doi.org/10.1515/jbcr-2015-0168.

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Summary Congenital cystic adenomatoid malformation (CCAM) is a rare abnormality of lung development. It was classified into 5 types by Stocker in 2002 and is also known under the name of congenital pulmonary airway malformation (CPAM). Cases are typically identified prenatally by routine ultrasonography screening. CCAM may present in the older child and adult as an incidental finding. The case presented is of a 21-year-old male patient who suffered from pulmonary infections with a recurrent productive cough 3-4 times the last 4 years. CT scanning of the thorax showed multiple cystic lesions in

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Pittman, Liz. "Congenital Cystic Adenomatoid Malformation of the Lung." Neonatal Network 21, no. 3 (2002): 59–66. http://dx.doi.org/10.1891/0730-0832.21.3.59.

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CONGENITAL CYSTIC ADENOMATOID malformation (CCAM) of the lung is a rare, multicystic lesion with embryonic origins. Approximately 421 cases have been documented since the lesion was first described in 1949.1 Usually, only one lobe is affected, most often the lower lobe.2 CCAM represents 25 percent of all congenital lung lesions.3 There is no race predominance, nor is there a left- or right-side trend.4 Males may be at greater risk than females for CCAM development.5

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Aouraghe, H., I. Filali, L. Chtouki, and A. Bentahila. "Congenital Cystic Adenomatoid Malformation: A Case Report." Asian Journal of Pediatric Research 13, no. 2 (2023): 16–20. http://dx.doi.org/10.9734/ajpr/2023/v13i2257.

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The case report is being done to increase the knowledge of Congenital Cystic Adenomatoid Malformation (CCAM) along with to better understand about the disease and its management & raise awareness. A female infant (aged 9 months and birth weight 2500 gm) was selected as participant. After physical examination, the state of the participant was good (fever:37.6ºC, heart rate: 120/min, respiratory rate: 40/min). Holding a good health certificate, a cystic image was identified at pulmonary artery in chest X-ray report. The histology findings were consistent with CPAM Type I. CPAM surgery, gener

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Shilo, Konstantin, Joseph F. Tomashefski, and Yao Chang Liu. "Congenital Cystic Adenomatoid Malformation of the Lung." Archives of Pathology & Laboratory Medicine 124, no. 11 (2000): 1720. http://dx.doi.org/10.5858/2000-124-1720-ccamot.

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