Relevant bibliographies by topics / Congenital cystic adenomatoid malformations

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  1. Journal articles
  2. Dissertations / Theses
  3. Book chapters
  4. Conference papers

Academic literature on the topic 'Congenital cystic adenomatoid malformations'

Author: Grafiati
Published: 3 June 2025
Last updated: 31 July 2025

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Journal articles on the topic "Congenital cystic adenomatoid malformations"

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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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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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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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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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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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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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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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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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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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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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Dissertations / Theses on the topic "Congenital cystic adenomatoid malformations"

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Ferreira, Hylas Paiva da Costa. "Tratamento cirúrgico das malformações pulmonares congênitas em pacientes pediátricos." reponame:Biblioteca Digital de Teses e Dissertações da UFRGS, 2009. http://hdl.handle.net/10183/27785.

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Objetivo: Analisar os principais achados do tratamento cirúrgico das malformações congênitas pulmonares em um serviço de cirurgia torácica pediátrica. Métodos: Foram revisados cinqüenta e dois prontuários de pacientes com diagnóstico anatomopatológico de malformações congênitas pulmonares que foram submetidos à ressecção pulmonar, no período de janeiro de 1997 a dezembro de 2006. Deste total, 39 casos eram de pacientes menores de 12 anos. Quatro casos foram excluídos, por prontuário incompleto. Resultados: Dos 35 pacientes estudados, a média de idade foi de 31 meses com predominância do sexo m
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Pott, Bärtsch Eva Maria. "Congenital cystic adenomatoid malformation of the lung (CCAM) and Bronchopulmonary sequestration (BPS): Prenatal diagnosis, pre- and postnatal interventions, and early- and long-term outcome (14 years clinical experience with 60 patients)." Diss., lmu, 2009. http://nbn-resolving.de/urn:nbn:de:bvb:19-108746.

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Freitas, Rogério Caixeta Moraes de. "Estudo do volume pulmonar fetal na predição da morbidade neonatal em pacientes com lesão pulmonar congênita." Universidade de São Paulo, 2016. http://www.teses.usp.br/teses/disponiveis/5/5139/tde-24102016-160727/.

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Introdução: A maioria dos fetos com lesão pulmonar congênita (LPC) são assintomáticos e apresentam baixa morbidade ao nascimento. No entanto, alguns neonatos apresentam desconforto respiratório e necessitam receber de cuidados especiais neste período. Decidir quais casos com LPC precisam nascer em um centro de referência é um desafio. Objetivo: O objetivo deste estudo foi predizer a morbidade neonatal em fetos com LCP sem hidropisia avaliados pela ultrassonografia tridimensional (US3D). Método: Estudo observacional, entre janeiro de 2005 e janeiro de 2016, com fetos com LPC e sem hidropisia. O
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Oliveira, Nuno Miguel Medeiros. "Congenital cystic adenomatoid malformation: the experience of a level III Neonatal Intensive Care Unit." Master's thesis, 2016. https://repositorio-aberto.up.pt/handle/10216/89756.

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Oliveira, Nuno Miguel Medeiros. "Congenital cystic adenomatoid malformation: the experience of a level III Neonatal Intensive Care Unit." Dissertação, 2016. https://repositorio-aberto.up.pt/handle/10216/89756.

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Vilaverde, Laura Catarina Simões. "Congenital Pulmonary Airway Malformation in Adults and Mucinous Adenocarcinoma." Master's thesis, 2021. http://hdl.handle.net/10316/98353.

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Trabalho Final do Mestrado Integrado em Medicina apresentado à Faculdade de Medicina<br>A malformação congénita das vias aéreas pulmonares (MCVAP), é a malformação congénita pulmonar mais comum, diagnosticada no período pré-natal ou em recém-nascidos sintomáticos, é rara na idade adulta. Uma série de MCVAP em adultos foi diagnosticada no Centro Hospitalar e Universitário de Coimbra - Portugal, durante doze anos (desde 2008 a 2019). Foi desenvolvida uma análise descritiva de 27 casos que foram revistos relativamente a achados clínicos, radiológicos e histopatológicos, reportando-se também a inc
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Pott, Bärtsch Eva Maria [Verfasser]. "Congenital cystic adenomatoid malformation of the lung (CCAM) and Bronchopulmonary sequestration (BPS) : prenatal diagnosis, pre- and postnatal interventions, and early- and long-term outcome (14 years clinical experience with 60 patients) / vorgelegt von Eva Maria Pott Bärtsch." 2009. http://d-nb.info/999586696/34.

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Book chapters on the topic "Congenital cystic adenomatoid malformations"

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Tovar, Juan A. "Congenital Cystic Adenomatoid Malformations." In Pediatric Thoracic Surgery. Springer Milan, 2013. http://dx.doi.org/10.1007/978-88-470-5202-4_21.

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Al-Salem, Ahmed H. "Congenital Cystic Adenomatoid Malformation." In An Illustrated Guide to Pediatric Surgery. Springer International Publishing, 2014. http://dx.doi.org/10.1007/978-3-319-06665-3_51.

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Al-Salem, Ahmed H. "Congenital Cystic Adenomatoid Malformation." In Atlas of Pediatric Surgery. Springer International Publishing, 2020. http://dx.doi.org/10.1007/978-3-030-29211-9_32.

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Brooks, A., and C. Ackermann. "Congenital Cystic Adenomatoid Malformation (CCAM)." In ABC of Pediatric Surgical Imaging. Springer Berlin Heidelberg, 2010. http://dx.doi.org/10.1007/978-3-540-89385-1_12.

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Becker, M. R., F. Schindera, and W. A. Maier. "Congenital Cystic Adenomatoid Malformation of the Lung." In Trachea and Lung Surgery in Childhood. Springer Berlin Heidelberg, 1987. http://dx.doi.org/10.1007/978-3-642-71665-2_15.

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Stocker, JT, JE Madewell, and RM Drake. "Congenital Cystic Adenomatoid Malformation of the Lung. Classification and Morphologic Spectrum." In 50 Landmark Papers every Pediatric Surgeon Should Know. CRC Press, 2023. http://dx.doi.org/10.1201/b23252-32.

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Wylam, Mark. "Miscellaneous Chest Abnormalities Affecting the Heart: Diaphragmatic Hernia and Eventration; Congenital Cystic Adenomatoid Malformation of the Lung." In Visual Guide to Neonatal Cardiology. John Wiley & Sons Ltd, 2018. http://dx.doi.org/10.1002/9781118635520.ch56.

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Paladini, Dario, and Paolo Volpe. "Posterior Cranial Fossa Cystic Malformations." In Ultrasound of Congenital Fetal Anomalies, 3rd ed. CRC Press, 2024. http://dx.doi.org/10.1201/9781003048268-10.

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Paladini, Dario, and Paolo Volpe. "Posterior Cranial Fossa Non-Cystic Malformations." In Ultrasound of Congenital Fetal Anomalies, 3rd ed. CRC Press, 2024. http://dx.doi.org/10.1201/9781003048268-11.

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Watanabe, Toshihiko. "Perinatal Natural History and Treatment of Congenital Lung Malformations in Prenatally Diagnosed Neonates." In Congenital Cystic Lung Disease. Springer Singapore, 2020. http://dx.doi.org/10.1007/978-981-15-5175-8_7.

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Conference papers on the topic "Congenital cystic adenomatoid malformations"

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Pranindya Sari, A., M. Elhidsi, S. H. Mety, A. Ghozali, and D. S. Heriyanto. "Congenital Cystic Adenomatoid Malformation: A Case Report." In American Thoracic Society 2020 International Conference, May 15-20, 2020 - Philadelphia, PA. American Thoracic Society, 2020. http://dx.doi.org/10.1164/ajrccm-conference.2020.201.1_meetingabstracts.a5377.

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Yonker, Lael, Eugene J. Mark, and Craig A. Canapari. "Aspergilloma In A Patient With An Occult Congenital Cystic Adenomatoid Malformation." In American Thoracic Society 2011 International Conference, May 13-18, 2011 • Denver Colorado. American Thoracic Society, 2011. http://dx.doi.org/10.1164/ajrccm-conference.2011.183.1_meetingabstracts.a1872.

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Kika, N., N. Patel, and R. Minkin. "A Rare Case of Adult Diagnosis of Congenital Cystic Adenomatoid Malformation." In American Thoracic Society 2022 International Conference, May 13-18, 2022 - San Francisco, CA. American Thoracic Society, 2022. http://dx.doi.org/10.1164/ajrccm-conference.2022.205.1_meetingabstracts.a5124.

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Boubaker, N., M. Abdennadher, H. Zribi, et al. "Congenital cystic adenomatoid malformation of lung in adults: A report of 7 cases." In ERS International Congress 2022 abstracts. European Respiratory Society, 2022. http://dx.doi.org/10.1183/13993003.congress-2022.3667.

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Cook, James, Lyn S. Chitty, Paolo De Coppi, Michael Ashworth, and Colin Wallis. "Prenatally diagnosed congenital cystic adenomatoid malformation (CCAM) and pulmonary sequestration (PS): Long-term follow-up of 119 cases." In ERS International Congress 2016 abstracts. European Respiratory Society, 2016. http://dx.doi.org/10.1183/13993003.congress-2016.pa3146.

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Chołubek, Michał, and Andrzej Materniak. "Cystic malformations of the posterior fossa: congenital causes and their differential diagnosis." In Radiopaedia 2025 Virtual Conference. Radiopaedia.org, 2025. https://doi.org/10.53347/rposter-3150.

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Martinez, M., S. Welsh, C. W. Lillehei, C. J. Smithers, H. P. W. Kozakewich, and L. P. Hayden. "Not All Mixed Cystic and Solid Lung Lesions Are Congenital Pulmonary Malformations: A Case of an Isolated Pulmonary Infantile Hemangioma." In American Thoracic Society 2019 International Conference, May 17-22, 2019 - Dallas, TX. American Thoracic Society, 2019. http://dx.doi.org/10.1164/ajrccm-conference.2019.199.1_meetingabstracts.a5012.

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