Pulmonary Arteriovenous Malformations

[Pulmonary arteriovenous fistulas in a pediatric patient: a case report]

Yuli T. Samboni, Liliana P. Tordecilla, Gilberto Acuña, Ana L. MuñozUniversidad Antonio Nariño.Columbia Archivos Argentinos de PediatriaArch Argent Pediatr 2020; 118: e170-e173DOI: 10.5546/aap.2020.e170 AbstractPulmonary arteriovenous fistulas are congenital malformations due to anomalous direct communication between arteries and veins; the incidence is 2-3:100,000 inhabitants. This condition is usually asymptomatic and incidentally appearing in adult imaging findings. Transcutaneous

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CT Angiography Findings of Pulmonary Arteriovenous Malformations in Children and Young Adults With Hereditary Hemorrhagic Telangiectasia

Su-Mi Shin, Hee Kyung Kim, Eric J. Crotty, Adrienne M. Hammill, Katherine Wusik, Dong-Hoon KimSMG-SNU Boramae Medical Center. Cincinnati Children’s Hospital Medical Center and University of Cincinnati College of Medicine. Korea University College of Medicine.Republic of Korea and United States American Journal of RoengenologyAJR Am J Roentgenol 2020; 214: 1369-1376DOI: 10.2214/AJR.19.22012 AbstractObjective. The purpose of this study

CT Angiography Findings of Pulmonary Arteriovenous Malformations in Children and Young Adults With Hereditary Hemorrhagic Telangiectasia Read More »

[Cyanosis for more than 4 years in a girl aged 4 years and 3 months]

Mao-Lan Wu, Xiang-Rong Zheng, Yan-Tong Zhu, Guo-Yuan Zhang, Chen-Tao Liu, Xia Wang, Yong-Jun TangXiangya Hospital and Central South University.China Chinese Journal of Contemporary PediatricsZhongguo Dang Dai Er Ke Za Zhi 2020; 22: 387-390DOI: 10.7499/j.issn.1008-8830.1910147 AbstractA girl, aged 4 years and 3 months, presented with cyanosis of the lips shortly after birth. She then experienced shortness of

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Pulmonary Arteriovenous Malformations in Non-hereditary Hemorrhagic Telangiectasia Patients: An 18-Year Retrospective Study

Hasan Ahmad Hasan Albitar, Justin M. Segraves, Yahya Almodallal, Catarina Aragon Pinto, Alice Gallo De Moraes, Vivek N. IyerMayo Clinic. Baylor College of Medicine. United States LungLung 2020; 98: 679-686DOI: 10.1007/s00408-020-00367-w AbstractPurpose: Pulmonary arteriovenous malformations (PAVMs) are most commonly associated with hereditary hemorrhagic telangiectasia (HHT). Patients with PAVMs can present with serious complications including stroke, transient ischemic

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Hepatic Vein Blood Increases Lung Microvascular Angiogenesis and Endothelial Cell Survival-Toward an Understanding of Univentricular Circulation

Andrew D. Spearman, Ankan Gupta, Amy Y. Pan, Emily I. Gronseth, Karthikeyan Thirugnanam, Todd M. Gudausky, Susan R. Foerster, Ramani RamchandranMedical College of Wisconsin and Children’s Hospital of Wisconsin.United States Seminars in Thoracic and Cardiovascular SurgerySemin Thorac Cardiovasc Surg 2020; 32: 980-987DOI: 10.1053/j.semtcvs.2020.03.004 AbstractTo improve our understanding of pulmonary arteriovenous malformations in univentricular congenital heart disease,

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Hereditary hemorrhagic telangiectasia and pulmonary arteriovenous malformations

Saniye Girit, Ebru Senol, Özge Karatas, Ayse Inci YıldırımIstanbul Medeniyet University. Göztepe Training and Research Hospital. University of Health Sciences Medical School Dr. Lutfi Kırdar Kartal Educational and Research Hospital. University of Health Sciences Medical School Kartal Kosuyolu High Speciality Educational and Research Hospital.Turkey Respiratory Medicine Case ReportsRespir Med Case Rep 2020; 30: DOI: 10.1016/j.rmcr.2020.101137 AbstractPulmonary

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Homozygous GDF2-Related Hereditary Hemorrhagic Telangiectasia in a Chinese Family

Jinrong Liu, Jigang Yang, Xiaolei Tang, Huimin Li, Yuelin Shen, Weiyue Gu, Shunying ZhaoBeijing Children’s Hospital, National Center for Children’s Health and Capital Medical University. Beijing Friendship Hospital. Beijing Chigene Translational Medicine Research Center.China PediatricsPediatrics 2020; DOI: 10.1542/peds.2019-1970 AbstractHereditary hemorrhagic telangiectasia (HHT) can be clinically diagnosed, but children often lack characteristic features. We report a family

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Incidental diagnosis of four pulmonary arteriovenous fistulas during patent foramen ovale closure: a case report

Alessandro Andreis, Gabriella Agnoletti, Paolo ScacciatellaCittà della Salute e della Scienza di Torino Hospital and University of Turin.Italy Cardiology in the YoungCardiol Young 2020; 30: 1363-1365DOI: 10.1017/S1047951120002152 Abstractryptogenic cerebral ischemia in young patients is commonly ascribed to paradoxical embolism. We report the clinical case of a young patient with cryptogenic stroke and a patent foramen ovale,

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Pulmonary arteriovenous malformation in a pediatric patient with epistaxis and hypoxemia

Ryan W. England, Clifford R. WeissJohns Hopkins Hospital.United States Radiology Case ReportsRadiol Case Rep 2020; 15: 1759-1763DOI: 10.1016/j.radcr.2020.07.026 AbstractHereditary hemorrhagic telangiectasia (HHT; also known as Osler-Weber-Rendu syndrome) is an inherited vascular disorder with a spectrum of clinical manifestations depending on lesion distribution. Epistaxis, mucocutaneous telangiectasia, and gastrointestinal bleeding are most common. Patients with pulmonary arteriovenous malformations

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[Case report of hereditary hemorrhagic telangiectasia in children and literature review]

Liu Jinrong, Liu Hui, Wang Bei, Zhang Yuhe, Xu Hui, Tang Xiaolei, Li Huimin, Zhao ShunyingBeijing Children’s Hospital Affiliated to Capital Medical University and National Center for Children’s Health. Beijing Renhe Hospital.China Chinese Journal of PediatricsZhonghua Er Ke Za Zhi 2020; 58: 674-678DOI: 10.3760/cma.j.cn112140-20200415-00386 AbstractObjective: To analyze the clinical features of 2 children with hereditary hemorrhagic telangiectasia (HHT) and review relevant literature. Methods: The clinical data of

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