Abnormal Systemic to Pulmonary Arterial Collaterals or Connections

Surgical ductal stent implantation in total anomalous pulmonary venous connection to vena porta with right pulmonary sequestration in a mature newborn

Huseyin Avni Solguna, Tugcin Bora PolatAltınbas University Medical Park and Bahcelievler Hospital.Turkey Annals of Medicine and SurgeryAnn Med Surg 2019; 45: 33-35DOI: 10.1016/j.amsu.2019.07.005 AbstractIn many cases of total anomalous pulmonary venous connection (TAPVC), the four pulmonary veins (PV) join together behind the left atrium, where they form a collector. This collector can drain into the right […]

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Digenic Inheritance in a Case of Pulmonary Arterial Hypertension Associated with Two Incidental Septal Defects and Multiple Thoracic Collaterals

Alejandro Cruz-Utrilla, María Pilar Escribano Subias, Jair Antonio Tenorio Castaño, María Jesús del Cerro MarínHospital Universitario 12 de Octubre, Madrid.  Instituto de Salud Carlos III.  Hospital Universitario La Paz.  European Reference Network on Rare Congenital Malformations and Rare Intellectual Disability. Ramón y Cajal University Hospital.Spain and Belgium Archivos de BronconeumologiaArch Bronconeumol 2023; 59: 169-170DOI: 10.1016/j.arbres.2022.09.006 AbstractNo

Digenic Inheritance in a Case of Pulmonary Arterial Hypertension Associated with Two Incidental Septal Defects and Multiple Thoracic Collaterals Read More »

Systemic artery to pulmonary artery aneurysm malformations associated with variants at MCF2L

S.E. Mitchell, R. P. Martin, P. Terry, S. E. Drant, D. Valle, H. Dietz, N. SobreiraJohns Hopkins University School of Medicine. Children’s Hospital of Philadelphia. United States American Journal of Medical GeneticsAm J Med Genet 2023; 191: 1250-1260DOI: 10.1002/ajmg.a.63141 AbstractArteriovenous malformations (AVM) are characterized by abnormal vessels connecting arteries and veins resulting in a disruption of

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Arterial Embolization and Methylene Blue Injection into the Aberrant Artery in Two Infants with Intralobar Sequestration

Anna Ayako Accarain, Marc Laureys, Luc Joyeux, Nasroola Damry, Henri Steyaert, Helena ReusensUniversité Libre de Bruxelles. Brugmann University Hospital. Hopital Universitaire des Enfants Reine Fabiola.Belgium European Journal of Pediatric Surgery ReportsEur J Pediatr Surg Rep 2022; 10: e141-e144DOI: 10.1055/s-0042-1757570 AbstractBronchopulmonary sequestration is a rare congenital lung dysplasia. An intralobar sequestration (ILS) is a nonfunctional mass within

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Successful occlusion of a feeding artery with Amplatzer Piccolo Occluder in a patient diagnosed with Scimitar syndrome

Hazim Alper Gursu, Bilal Ozelce, Ibrahim Ilker CetinAnkara City Hospital. Yıldırım Beyazıt University.Turkey Cardiology in the YoungCardiol Young 2022; DOI: 10.1017/S1047951122001172 AbstractScimitar syndrome is a congenital anomaly in which some or all of right pulmonary veins drain into inferior caval vein. It is associated with anomalous systemic arteries arising from descending aorta supplying to right lung.

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Isolated partial anomalous origin of a branch pulmonary artery from the descending aorta

Wei-Li Liu, Ming-Chih Lin, Sheng-Ling JanDalin Tzu Chi Hospital. Children’s Medical Center and Taichung Veterans General Hospital. National Yang-Ming University. Kaohsiung Medical University.Taiwan Cardiology in the YoungCardiol Young 2022; 32: 648-651DOI: 10.1017/S1047951121003346 AbstractThe condition of partial anomalous origin of a branch pulmonary artery from the descending aorta could be found in several diseases and should be

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Thoracoscopic Clockwise Lobectomy May Be a Stylized Procedure for Treating Children with Congenital Lung Malformations

Dengke Luo, Xiaoying Fu, Qinghai Wang, Kaisheng Cheng, Yong Lv, Miao Yuan, Chang Xu, Taozhen He, Gang Yang, Yao Wang, Ru Jia, Chenyu LiuWest China Hospital and Sichuan University. Guangyuan Central Hospital.China Journal of Laparoendoscopic and Advanced Surgical TechniquesJ Laparoendosc Adv Surg Tech 2022; 32: 1293-1298DOI: 10.1089/lap.2022.0078 AbstractBackground: Thoracoscopic lobectomy is a challenging procedure in children with

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Giant Feeding Artery from Abdominal Aorta in Intralobar Pulmonary Sequestration

Anita Singh, Ankur Mandelia, Prabha Verma, Kirti Naranje, Girish GuptaSanjay Gandhi Postgraduate Institute of Medical Sciences. Himalayan Institute of Medical Sciences and Swami Rama Himalayan University.India Journal of Indian Association of Pediatric SurgeryJ Indian Assoc Pediatr Surg 2022; 27: 270-272DOI: 10.4103/jiaps.JIAPS_372_20 AbstractPulmonary sequestration (PS) is a rare congenital lung malformation. We present a case of newborn

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‘Hybrid’ Bronchopulmonary Malformation – Lobar Emphysema and Extra Lobar Sequestration

Thattaruparambil Prakash Vinayak, Suravi Mohanty, Kanishka DasAll India Institute of Medical Sciences. St. John’s Medical College. India Fetal and Pediatric PathologyFetal Pediatr Pathol 2022; 41: 505-510DOI: 10.1080/15513815.2020.1849474 AbstractBackground: Idiopathic lobar emphysema (ILE) and bronchopulmonary sequestration (BPS) are two of the well-characterized pulmonary malformations. Case report: An antenatally detected case of a left bronchopulmonary malformation (BPM) was clinicoradiologically diagnosed to

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Ten-year experience in the clinical management of intralobar pulmonary sequestration in children

Chenyu Liu, Kaisheng Cheng, Taozhen He, Miao Yuan, Dengke Luo, Chang XuWest China Hospital of Sichuan University.China Pediatric PulmonologyPediatr Pulmonol 2023; 58: 1022-1027DOI: 10.1002/ppul.26287 AbstractObjectives: Intralobar pulmonary sequestration (ILS) is rare and its optimal clinical management remains ambiguous. This study aimed to introduce our 10-year experience in clinical management of ILS. And the application of our novel

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