Abnormal Systemic to Pulmonary Arterial Collaterals or Connections

Extralobar sequestration with a pulmonary arterial feeding vessel

Daisuke Nakamura, Ryoichi Kondo, Akiko Makiuchi, Hiroko ItagakiNational Hospital Organization Matsumoto Medical Center. Japan General Thoracic and Cardiovascular SurgeryGen Thorac Cardiovasc Surg 2021; 69: 160-162DOI: 10.1007/s11748-020-01443-x AbstractExtralobar sequestrations are rare congenital malformations of the lung. They are usually located between the diaphragm and left lower lobe and receive their blood supply from the aorta. We report […]

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A Rare Variant of Hypogenetic Lung Syndrome Mimicking Scimitar Vein

Tommaso D’Angelo, Alfredo Blandino, Michele B. Saitta, Salvatore Agati, Placido Romeo, Silvio MazziottiG. Martino University Hospital Messina. Bambino Gesù Children’s Hospital.Italy Annals of Thoracic SurgeryAnn Thorac Surg 2021; 112: e173-e176DOI: 10.1016/j.athoracsur.2021.01.020 AbstractHypogenetic lung syndrome, also known as scimitar syndrome, is a rare and well-known congenital condition that includes hypoplastic right pulmonary artery and lung, right displacement

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Unilateral Branch Pulmonary Artery Origin From a Solitary Arterial Trunk With Major Aortopulmonary Collaterals to the Contralateral Lung: Anatomic and Developmental Considerations

Gregory T. Adamson, Lucile Houyel, Doff B. McElhinney, Shiraz A. Maskatia, Michael Ma, Frank L. Hanley, Leo LopezStanford University School of Medicine. Hôpital Necker Enfants Malades.United States and France Seminars in Thoracic and Cardiovascular SurgerySemin Thorac Cardiovasc Surg 2021; 33: 780-786DOI: 10.1053/j.semtcvs.2020.11.009 AbstractIn both truncus arteriosus communis (TAC) and tetralogy of Fallot (TOF), there is a

Unilateral Branch Pulmonary Artery Origin From a Solitary Arterial Trunk With Major Aortopulmonary Collaterals to the Contralateral Lung: Anatomic and Developmental Considerations Read More »

Systemic to Pulmonary Collaterals in Extremely Low Birth Weight Infants: Incidence, Clinical Significance, and Hemodynamic Features

Cynthia Hayek, Rowena Cayabyab, Ima Thompson, Mahmood Ebrahimi, Bijan Siassi, Rangasamy RamanathanLos Angeles County and University of Southern California Medical Center.  Children’s Hospital Los Angeles and University of Southern California.United States American Journal of PerinatologyAm J Perinatol 2021; 38: 145-149DOI: 10.1055/s-0039-1695012 AbstractObjective: This study aimed to determine the incidence of systemic to pulmonary collaterals (SPCs) in extremely low birth weight infants

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Congenital isolated unilateral agenesis of pulmonary arteries in adults: case series and review

Pankaj Jariwala, Venkata Nagarjuna Maturu, Johann Christopher, Kartik Pandurang JadhavYashoda Hospitals. Care Hospitals.India Indian Journal of Thoracic and Cardiovascular SurgeryIndian J Thorac Cardiovasc Surg 2021; 37 (Suppl 1): 144-154DOI: 10.1007/s12055-020-01032-w AbstractCongenital, isolated unilateral agenesis of pulmonary arteries (UAPA) has a bimodal clinical presentation. It is either diagnosed in early infancy or during adulthood. Early diagnosis and

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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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