Symptoms and Findings Associated with Pulmonary Vascular Disease

Burden of pulmonary arterial hypertension in children globally, regionally, and nationally (1990-2021): results from the global burden of disease study

Lili Deng, Jingxuan Xiong, Jiaoli Xu, Qinhong Li, Zugen ChengKunming Children’s Hospital. First Affiliated Hospital of Kunming Medical University. China Frontiers in PediatricsFront Pediatr 2025; DOI: 10.3389/fped.2025.1527281 AbstractIntroduction: Pediatric pulmonary arterial hypertension (PAH) is a rare and severe disorder characterized by obstructive vascular changes that can lead to right heart failure. The clinical presentation and underlying causes […]

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Anxiety and Depression Screening of Youth in Pediatric Pulmonary Hypertension Clinic: A Multi-Center, Cross-Sectional Study

Claire Parker, Elise Whalen, Michael A. Smith, Jasmine Becerra, Leah Stevens, Catherine M. Avitabile, Anna Brown, Michelle Cash, Emma Olson Jackson, Julia McSweeney, Kathleen Miller‐Reed, Janette T. Reyes, Cathy Sheppard, Mary P. Mullen, Pulmonary Hypertension Network (PPHNet)University of California, San Francisco and Benioff Children’s Hospital. Texas Children’s Hospital. University of Pennsylvania Perelman School of Medicine

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Clinical Phenotypes of a Pediatric Cohort with GDF2-Related Hereditary Hemorrhagic Telangiectasia

Owen Oliver, Allison D. Britt, Alexandra J. Borst, Elizabeth Goldmuntz, Nihal Bakeer, Shih-shan Lang, Stephanie Fuller, Arastoo Vossough, Lauren A. BeslowChildren’s Hospital of Philadelphia and Perelman School of Medicine at the University of Pennsylvania. United States Journal of Clinical MedicineJ Clin Med 2025; 14: DOI: 10.3390/jcm14103359 AbstractBackground/Objectives: Pathogenic variants in the growth differentiation factor 2 (GDF2) gene

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Efficacy of Intravascular Therapeutic Hypothermia for Moderate to Severe Hypoxic-Ischemic Encephalopathy

Tomonori Kurimoto, Takuya Tokuhisa, Itaru Hayasaka, Tsuyoshi Yamamoto, Eiji Hirakawa, Hiroshi Ohashi, Masaya Kibe, Asataro Yara, Takatsugu Maeda, Masato Kamitomo, Satoshi IbaraKagoshima City Hospital. Nikko Memorial Hospital. Japan ChildrenChildren 2025; 12: DOI: 10.3390/children12050605 AbstractBackground/objectives: Hypoxic-ischemic encephalopathy (HIE), affecting 1.3-1.7/1000 live births, is treated with conventional therapeutic hypothermia (TH) but carries significant mortality and neurological impairment. Here, we

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[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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[Hereditary hemorrhagic telangiectasia: a report of two cases]

Yan Huang, Chen-Tao Liu, Xiang-Rong Zheng, Bo Dou, Rong HuangXiangya Hospital of Central South University.China Chinese Journal of Contemorary PediatricsZhongguo Dang Dai Er Ke Za Zhi 2020; 22: 1041-1042DOI: 10.7499/j.issn.1008-8830.2004196 AbstractThis article reports two children with hereditary hemorrhagic telangiectasia (HHT). Patient 1 was a boy aged 12 years and was admitted due to intermittent cough and

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A rare cause of newborn central cyanosis

Anna Waldoch, Robert Sabiniewicz, Joanna KwiatkowskaMedical University in Gdansk.Poland EchocardiographyEchocardiography 2020; 37: 1524-1525DOI: 10.1111/echo.14809 AbstractPulmonary arteriovenous malformations are rare congenital vascular anomalies. They are usually associated with congenital hemorrhagic hemangioma. The hemodynamic effect of fistulas depends on their size, as well as the location. The most common manifestations include central cyanosis, ischemic stroke, murmur over the

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Bronchial arteries to right pulmonary artery anastomoses in right pulmonary vein atresia

J. Fred Johnson, Andrew L Juris, Edith Valerie BarnesTripler Army Medical Center.United States Cardiovascular and Interventional RadiologyCardiovasc Interv Radiol 1982; 5: 238-240DOI: 10.1007/BF02565403 AbstractAbstract Not Available CategorySegmental Pulmonary Venous Disease. Without a Focus on Pulmonary HypertensionSymptoms and Findings Associated with Pulmonary Vascular DiseaseDiagnostic Testing for Pulmonary Vascular Disease. Invasive Testing Age Focus: Pediatric Pulmonary Vascular Disease

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Congenital atresia of unilateral pulmonary veins associated with a single ventricle: a rare case report and literature review

Hsing-Yuan Lee, Betau Hwang, Pi-Chang Lee, Sheng-Ling Jan, C.C. Laura MengTaoyuan Armed Force General Hospital.Taiwan Circulation JournalCirc J 2008; 72: 1544-1546DOI: 10.1253/circj.cj-07-0516 AbstractCongenital atresia or extreme hypoplasia of individual pulmonary veins is a rare condition that is usually asymptomatic if it only involves 1 or 2 segments of the lungs. It may be fatal if it

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