Pediatric Pulmonary Vascular Disease

Preservation of Antegrade Pulmonary Blood Flow in Kawashima Procedure With Prior Right Ventricular Outflow Tract Stent

Suneet Bhansali, Puneet Bhatla, Michael Argilla, Sunil Saharan, Ralph Mosca, Tk Susheel KumarLangone Medical Center.United States World Journal of Pediatric and Congenital Heart SurgeryWorld J Pediatr Congenit Heart Surg 2022; 13: 521-523DOI: 10.1177/21501351221080171 AbstractSurgical management of single ventricle with interrupted inferior vena cava and azygos continuation typically requires a Kawashima procedure with subsequent completion of Fontan. […]

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Pearls & Oy-sters: Cerebral Abscess Secondary to Pulmonary Arteriovenous Malformation in Hereditary Hemorrhagic Telangiectasia

Jodie I. Roberts, Kristine Woodward, Adam Kirton, Michael J. EsserUniversity of Calgary; Alberta Children’s Hospital Research Institute.Canada NeurologyNeurology 2022; 98: 292-295DOI: 10.1212/WNL.0000000000013181 AbstractHereditary hemorrhagic telangiectasia (HHT) is an autosomal dominant condition that is linked to a myriad of neurologic complications arising from vascular malformations of the brain, spinal cord, and lungs. Our case describes a previously

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Hypoxia and Polycythemia: A Pediatric Emergency Department Point of Care Ultrasound Diagnosis of Pulmonary Arteriovenous Malformation

Shachar Oren, Shachar, Galit Brenner, Yael Garty, Eric ScheierKaplan Medical Center. Hebrew University of Jerusalem.Israel Pediatric Emergency CarePediatr Emerg Car 2022; 38: 633-635DOI: 10.1097/PEC.0000000000002721 AbstractPoint of care ultrasound (POCUS) can be useful in the differentiation between cardiac and pulmonary etiologies of hypoxia. Here, we present a child with signs of chronic hypoxia, found on POCUS to

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Pulmonary arteriovenous malformations: A case of missed diagnosis in a neonate

Zurina Zainudin, Nadiah Azlisham, Ghee Tiong Koh, Yinn Khurn Ooi, Melissa Anne NunisUniversiti Putra Malaysia. Hospital Pakar Sultanah Fatimah. Hospital Serdang.Malaysia Medical Journal of MalaysiaMed J Malaysia 2022; 77: 274-276DOI: Not available AbstractPulmonary arteriovenous malformation (PAVM) is a congenital vascular abnormality that can cause persistent cyanosis in children. PAVMs can go undetected till adulthood; however,

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Rare Cause of Hypoxemia in a Toddler: New Diagnosis of Hereditary Hemorrhagic Telangiectasia

Shikha Saxena, Patrick W. Doyle, Christopher M. Baron, Thomas P. Doyle, Andrew G. SokolowVanderbilt University Medical Center. United States American Journal of Respiratory and Critical Care MedicineAm J Respir Crit Care Med 2023; DOI: 10.1164/rccm.202209-1703IM AbstractAbstract not available CategoryPulmonary Arteriovenous Malformations Age Focus: Pediatric Pulmonary Vascular Disease Fresh or Filed Publication: Filed (PHiled). Greater than 1-2

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Transcatheter management of life-threatening pulmonary arteriovenous fistula with extracorporeal membrane oxygenation support in an infant

Osman Guvenc, Ender Odemis, Murat Saygi, M. Akif OnalanAcıbadem University. Koc University. Turkey Cardiology in the YoungCardiol Young 2023; 33: 498-501DOI: 10.1017/S1047951122002724 AbstractPulmonary arteriovenous malformation is a rare disease leading to cyanosis, where there is a direct relation between the pulmonary artery and pulmonary vein without a capillary structure. Arteriovenous fistulae may be single or multiple.

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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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