Class 3. Pulmonary Hypertension Associated with Lung Hypoplasia

The natural history of prenatally diagnosed congenital pulmonary airway malformations and bronchopulmonary sequestrations

Matilda Karlsson, Peter Conner, Henrik Ehren, Catrina Bitkover, Carmen Mesas BurgosKarolinska University Hospital. Sweden Journal of Pediatric SurgeryJ Pediatr Surg 2022; 57(: 282-287DOI: 10.1016/j.jpedsurg.2022.03.021 AbstractBackground: The natural history of congenital pulmonary airway malformations (CPAM) and bronchopulmonary sequestrations (BPS) is not fully understood, and the management of the newborn with an asymptomatic lesion is a controversial issue. We […]

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Thoracoscopic repair of neonatal left diaphragmatic hernia with sac combined with both extralobar pulmonary sequestration and congenital pulmonary airway malformation

Koji Yamada, Mitsuru Muto, Shun Onishi, Seiro Machigashira, Nanako Nishida, Ayaka Nagano, Masakazu Murakami, Koshiro Sugita, Keisuke Yano, Toshio Harumatsu, Waka Yamada, Makoto Matsukubo, Takafumi Kawano, Satoshi IeiriKagoshima University. Kagoshima City Hospital. Kagoshima University Hospital.Japan Asian Journal of Endoscopic SurgeryAsian J Endosc Surg 2022; 16: 127-130DOI: 10.1111/ases.13120 AbstractIntradiaphragmatic extralobar pulmonary sequestration (IDEPS) is considered to be

Thoracoscopic repair of neonatal left diaphragmatic hernia with sac combined with both extralobar pulmonary sequestration and congenital pulmonary airway malformation Read More »

Hybrid lung lesions in children with segmental infantile hemangiomas, a new association?

Omeed Modiri, Mahavrat Shaheen S. Malick, Margaret E. Scollan, Vincent Duron, Kimberly Morel, William Middlesworth, Maria C. GarzonColumbia University Medical Center and Vagelos College of Physicians and Surgeons.United States Pediatric DermatologyPediatr Dermatol 2023; 40: 144-147DOI: 10.1111/pde.15123 AbstractInfantile hemangiomas (IHs) are the most common tumors of infancy and, in rare instances, can present in the setting of

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Can we predict the need for postnatal surgery in patients with prenatal fetal lung masses detected by CVR value?

Aydin Ocal, Oya Demirci, Gizem Elif Dizdarogullari, Ozge Kahramanoglu, Isil Ayhan, Munip Akalin, Mucize Eric Ozdemir, Ali Sahap Odacilar, Umit Tasdemir, Aysenur CelayirHealth Science University and Zeynep Kamil Women and Children’s Diseases Training and Research Hospital,Istanbul. Turkey Journal of Gynecology Obstetrics and Human ReproductionJ Gynecol Obstet Hum Reprod 2023; DOI: 10.1016/j.jogoh.2022.102526 AbstractAim: The purpose of this study

Can we predict the need for postnatal surgery in patients with prenatal fetal lung masses detected by CVR value? Read More »

Prenatal ultrasound-and MRI-based imaging predictors of respiratory symptoms at birth for congenital lung malformations

Claire Cerall, Ritah Chumdermpadestuk, Shimon Jacobs, Fan Weijia, Alexis Maddocks, Rama Ayyala, Lyn Simpson, Steven Rothenberg, Vincent DuronColumbia University Vagelos College of Physicians and Surgeons and NewYork-Presbyterian Morgan Stanley Children’s Hospital. NYU Grossman School of Medicine. Columbia University Mailman School of Public Heath. Cincinnati Children’s Hospital. Rocky Mountain Hospital for Children.United States Journal of Pediatric

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Morphologic Features in Congenital Pulmonary Airway Malformations and Pulmonary Sequestrations Correlate With Mutation Status: A Mechanistic Approach to Classification

Nya D. Nelson, Feng Xu, William H. Peranteau, Marilyn Li, Jennifer PogorilerHospital of the University of Pennsylvania. The Children’s Hospital of Philadelphia and Perelman School of Medicine at the University of Pennsylvania.United States American Journal of Surgical PathologyAm J Surg Pathol 2023; 47: 568-579DOI: 10.1097/PAS.0000000000002025 AbstractCongenital pulmonary airway malformations (CPAMs) have a range of morphologies with

Morphologic Features in Congenital Pulmonary Airway Malformations and Pulmonary Sequestrations Correlate With Mutation Status: A Mechanistic Approach to Classification Read More »

The long-term outcome following thoraco-amniotic shunting for congenital lung malformations

Ancuta Muntean, Ramona Cazacu, Niyi Ade-Ajayi, Shailesh B Patel, Kypros Nicolaides, Mark DavenportKings College Hospital. United Kingdom Journal of Pediatric SurgeryJ Pediatr Surg 2023; 58: 213-217DOI: 10.1016/j.jpedsurg.2022.10.028 AbstractAim of the study: Insertion of a thoraco amniotic shunt (TAS) during fetal life is a therapeutic option where there is a high risk of death secondary to large congenital

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Innovative Fetal Therapy for a Giant Congenital Pulmonary Airway Malformation with Hydrops

Denise B. Klinkner, Thomas Atwell, Ayssa Teles Abrao Trad, Matthew R. Callstrom, Mohamed Yasir Qureshi, Ellen Bendel Stenzel, Mauro Schenone, Rodrigo RuanoMayo Clinic. University of Miami.United States Fetal Diagnosis and TherapyFetal Diagn Ther 2022; 49: 250-255DOI: 10.1159/000521690 AbstractIntroduction: Congenital pulmonary airway malformations (CPAMs) complicated by hydrops portend significant morbidity and mortality, with fetal survival estimates less than

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Identification of SOX2 Interacting Proteins in the Developing Mouse Lung With Potential Implications for Congenital Diaphragmatic Hernia

Kim A. A. Schilders, Gabriëla G. Edel, Evelien Eenjes, Bianca Oresta, Judith Birkhoff, Anne Boerema-de Munck, Marjon Buscop-van Kempen, Panagiotis Liakopoulos, Petros Kolovos, Jeroen A. A. Demmers, Raymond Poot, Rene M. H. Wijnen, Dick Tibboel and Robbert J. RottierErasmus Medical Center and Sophia Children’s Hospital. Democritus University of Thrace. Netherlands and Greece Frontiers in PediatricsFront

Identification of SOX2 Interacting Proteins in the Developing Mouse Lung With Potential Implications for Congenital Diaphragmatic Hernia Read More »

Expected small left heart size in the presence of congenital diaphragmatic hernia: Fetal values and Z-scores for infants confirmed to have no heart disease postnatally

Anita J. Moon-Grady, Francesca A. Byrne, Leslie A. Lusk, Roberta L. KellerUniversity of California San Francisco and Benioff Children’s Hospital.United States Frontiers in PediatricsFront Pediatr 2022; DOI: 10.3389/fped.2022.1083370 AbstractObjectives: In fetuses with left-sided congenital diaphragmatic hernia (CDH), left heart structures may appear small, but usually normalize after birth in the absence of structural cardiac anomalies. To decrease

Expected small left heart size in the presence of congenital diaphragmatic hernia: Fetal values and Z-scores for infants confirmed to have no heart disease postnatally Read More »

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