Filed (PHiled). Greater than 1-2 years since publication

Novel Diabolo Configuration of a Large Covered Stent to Treat Cyanosis Related to Pulmonary Arteriovenous Malformations

Sarosh P. Batlivala, Amr Matoq, Shabana ShahanavazUniversity of Cincinnati College of Medicine and Cincinnati Children’s Hospital Medical Center.United States World Journal of Pediatric and Congenital Heart SurgeryWorld J Pediatr Congenit Heart Surg 2023; DOI: 10.1177/21501351231162958 AbstractMicrovascular pulmonary arteriovenous malformations (pAVMs) can lead to profound hypoxemia. “Hepatic factor” is postulated to play a role in their development. […]

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Cystic fibrosis with multiple pulmonary arteriovenous malformations: A case report

Orito Ikeda, Kunihiko Shimizu, Yoshitake Yamada, Hiroaki Sugiura, Hideaki Suzuki, Syuichiro Umetsu, Kozo Sato, Masahiro JinzakiSaiseikai Yokohama-shi Tobu Hospital. Keio University School of Medicine. National Defense Medical College Hospital. Japan Radiology Case ReportsRadiol Case Rep 2023; 18: 1033-1036DOI: 10.1016/j.radcr.2022.12.024 AbstractCystic fibrosis is an autosomal recessive genetic disorder that damages the exocrine function of the body, resulting

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MRI as screening for pulmonary arteriovenous malformations in hereditary hemorrhagic telangiectasia

Shivanthan Shanthikumar, Elhamy Bekhit, Jenny BrackenMurdoch Children’s Research Institute. Royal Children’s Hospital. University of Melbourne.Australia Pediatric PulmonologyPediatr Pulmonol 2023; 58(4):1281-1282DOI: 10.1002/ppul.26297 AbstractAbstract not available CategoryPulmonary Arteriovenous MalformationsDiagnostic Testing for Pulmonary Vascular Disease. Non-invasive Testing Age Focus: Pediatric Pulmonary Vascular Disease Fresh or Filed Publication: Filed (PHiled). Greater than 1-2 years since publication Article Access Free PDF

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Interruption of the Right Pulmonary Artery in a Neonate

Mohammadreza Khalilian, Taraneh Faghihi Langroudi, Ali Dabbagh, Ramin Baghaei Tehrani, Tahmineh TahouriShahid Beheshti University of Medical Sciences.Iran Case Reports in CardiologyCase Rep Cardiol 2022; DOI: 10.1155/2022/7666677 AbstractInterruption of the right pulmonary artery is a very rare anomaly which can be associated with other congenital heart lesions or can occur in isolation. Clinical presentations of the unilateral

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Maternal Outcomes Among Pregnant Women With Congenital Heart Disease-Associated Pulmonary Hypertension

Qian Zhang, Fang Zhu, Guochen Shi, Chen Hu, Weituo Zhang, Puzhen Huang, Chunfeng Zhu, Hong Gu, Dong Yang, Qiangqiang Li, Yonghua Niu, Hao Chen, Ruixiang Ma, Ziyi Pan, Huixian Miao, Xin Zhang, Genxia Li, Yabing Tang, Guyuan Qiao, Yichen Yan, Zhongqun Zhu, Hao Zhang, Fangzhen Han, Yanna Li. Jianhua Lin, Huiwen ChenMultiple InstitutionsChina CirculationCirculation 2023;

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Right Pulmonary Artery Absence or Discontinuity in Ethiopian Toddler

Henok Tadele, Etsegenet GedluCollege of Health Sciences, Addis Ababa University.Ethiopia Ethiopian Journal of Health ScienceEthiop J Health Sci 2020; 30: 1043-1046DOI: 10.4314/ejhs.v30i6.24 AbstractBackground: Unilateral pulmonary artery absence or discontinuity is a rare congenital abnormality. Its reported prevalence is 1 in 150,000 adults.Case presentation: A 22-month-toddler girl was referred from a general hospital for cardiac follow-up to our hospital

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Repeat percutaneous recanalizations of a discontinuous pulmonary artery: A very “lucky” vessel

Giovanbattista Calabri, Alberto Clemente, Giuseppe Santoro“Meyer” Pediatric Hospital and University of Florence.”Ospedale del Cuore”. Heart Hospital “G. Pasquinucci”.Italy Annals of Pediatric CardiologyAnn Pediatr Cardiol 2020; 13: 163-166DOI: 10.4103/apc.APC_142_19 AbstractPulmonary artery (PA) discontinuity with ductal origin of a major pulmonary branch is a rare congenital anomaly that can be diagnosed as an isolated lesion or in association

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Bilateral Ductal Stenting for Discontinuity of the Pulmonary Artery via the Femoral and Carotid Arteries in an Infant

Osman Baspinar, Derya Aydin SahinGaziantep UniversityTurkey Case Reports in CardiologyCase Rep Cardiol 2015; DOI: 10.1155/2015/619653 AbstractBilateral ductal stenting should be performed in cases of discontinuity of the pulmonary branches and pulmonary atresia. Performing this procedure via the carotid artery in small infants can be very difficult and challenging. We present a case of bilateral ductal stenting

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Surgical repair of discontinuous right pulmonary artery utilising an autologous main pulmonary artery flap: a case report and literature review

Nibras El Sherif, Frank Cetta, Elizabeth H. StephensMayo Clinic.United States Cardiology in the YoungCardiol Young 2021; 31: 2038-2040DOI: 10.1017/S1047951121002018 AbstractThis is a case of an infant with unilateral discontinuous right pulmonary artery. Cardiac catheterisation with pulmonary wedge injection diagnosed the anomaly and aided in surgical planning. The patient underwent semi-autologous surgical repair utilising an autologous main

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Double-Outlet Right Ventricle, Pulmonary Atresia, and Discontinuous Branch Pulmonary Arteries Supplied by Bilateral Ducti

Kamel Shibbani, Bijoy Thattaliyath, Michael Bunker, Shafkat Anwar, Ravi AshwathUniversity of Iowa Stead Family Children’s Hospital. University of California-San Francisco, School of Medicine.United States Journal of the American College of Cardiology Case ReportsJACC Case Rep 2021; 3: 1236-1240DOI: 10.1016/j.jaccas.2021.04.020 AbstractWe present a rare case of double-outlet right ventricle with pulmonary atresia and discontinuous branch pulmonary arteries

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