Symptoms and Findings Associated with Pulmonary Vascular Disease

Demographic, hemodynamic characteristics, and therapeutic trends of pulmonary hypertension patients: The Pulmonary Hypertension Mexican registry (REMEHIP)

Carlos Jerjes‐Sánchez, Alicia Ramírez‐Rivera, Nayeli Zayas Hernandez, Guillermo Cueto Robledo, Humberto García‐Aguilar, Pedro Gutiérrez‐Fajardo, Mario Seoane García de León, Francisco Moreno Hoyos‐Abril, Miguel Ernesto Beltrán Gámez, Jose Elizalde, Tomás Pulido Fccp, Julio Sandoval, The REMEHIP InvestigatorsEscuela de Medicina y Ciencias de la Salud Monterey. TecSalud San Pedro Garza Garcia. Unidad de Investigación Clínica en Medicina S.C. […]

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Pulmonary hypertension in the intensive care unit after pediatric allogeneic hematopoietic stem cell transplant: incidence, risk factors, and outcomes

Michael A. Smith, Geoffrey Cheng, Rachel Phelan, Ruta Brazauskas, Joelle Strom, Kwang Woo Ahn, Betty Ky Hamilton, Andrew Peterson, Bipin Savani, Hélène Schoemans, Michelle L. Schoettler, Mohamed Sorror, Roberta L. Keller, Christine S. Higham, Christopher C. Dvorak, Jeffrey R. Fineman, Matt S. ZinterUniversity of California, San Francisco. Medical College of Wisconsin. Cleveland Clinic. Vanderbilt University

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Impact of Portal Flow on the Prognosis of Children With Congenital Portosystemic Shunt: A Multicentric Observation Study in Japan

Hajime Uchida, Masato Shinkai, Hiroomi Okuyama, Takehisa Ueno, Mikihiro Inoue, Toshihiro Yasui, Eiso Hiyama, Sho Kurihara, Yasunasru, Sakuma, Yukihiro Sanada, Akinobu, Taketomi, Shohei Honda, Motoshi Wada, Ryo Ando, Jun Fujishiro, Mariko Yoshida, Yohei Yamada, Hiroo Uchida, Takahisa Tainaka, Mureo Kasahara, Japanese Society of Pediatric Splenology PortalvenologyNational Center for Child Health and Development. Kanagawa Children’s Medical

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Multisystem Inflammatory Syndrome in Neonates Associated with COVID-19 in Neonatal ICU of a Tertiary Care Hospital

Asma Shabbir, Humaira Khurshid, Imran Mahmood KhanFazaia Medical College, Pakistan Air Force Hospital.Pakistan Journal of the College of Physicians and Surgeons PakistanJ Coll Physicians Surg Pak 2024; 34: 727-731 DOI: 10.29271/jcpsp.2024.06.727 AbstractObjective: Neonatal multisystem inflammatory syndrome (MIS-N) is a unique disease of neonates described in several case reports from all over the world with a myriad of

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The multisystem nature of isomerism: left isomerism complicated by Abernethy malformation and portopulmonary hypertension

Megan L. Ringle, Rohit Loomba, John C. Dykes, Danyal Khan, David Schidlow, Gil WernovskyLucile Packard Children’s Hospital and Stanford University School of Medicine. Advocate Children’s Hospital and Chicago Medical School. Nicklaus Children’s Hospital. Boston Children’s Hospital and Harvard Medical School. Children’s National Hospital.United States Cardiology in the YoungCardiol Young 2021; 31: 532-540DOI: 10.1017/S1047951121000809 AbstractIsomerism, also referred

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Phenotypic characterisation of SMAD4 variant carriers

Claire Caillot, Jean-Christophe Saurin, Valérie Hervieu, Marie Faoucher, Julie Reversat, Evelyne Decullier, Gilles Poncet, Sabine Bailly, Sophie Giraud, Sophie Dupuis-GirodFemme-Mère-Enfants Hospital and Hospices Civils de Lyon. Hôpital E. Herriot. Université Claude Bernard Lyon 1. France Journal of Medical GeneticsJ Med Genet 2024; DOI: 10.1136/jmg-2023-109632 AbstractBackground: Both hereditary haemorrhagic telangiectasia (HHT) and juvenile polyposis syndrome (JPS) are known

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Sudden pediatric death unveiling pulmonary arteriovenous malformations

Hadeel Abu-El-Rub, Rashed Shatnawi, Yahia I. Abu Zetun, Doaa Ghorab, Ali M. ShotarYarmouk University. Mansoura University. Jordan University of Science and Technology School of Medicine.Jordan Autopsy Case ReportsAutops Case Rep 2024; DOI: 10.4322/acr.2024.489 AbstractPulmonary arteriovenous malformations (PAVMs) are abnormal vascular connections between pulmonary arteries and veins, often associated with hereditary hemorrhagic telangiectasia (HHT). Most PAVMs are

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Neonatal pleural effusion associated with pulmonary sequestration: A case report

Sajal Twanabasu, Shiva Prasad Sharma ChalisePatan Academy of Health Sciences. Nepal Clinical Case ReportsClin Case Rep 2024; 12:DOI: 10.1002/ccr3.8956 AbstractPleural effusion is rare during neonatal period with an estimated prevalence of 0.06%. It may sometimes uncommonly be secondary to pulmonary sequestration. Besides common conditions like hydrops fetalis, congenital heart disease, congenital chylothorax, chromosomal abnormalities; pulmonary sequestration

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A Four-Week-Old Infant With Respiratory Distress: An Emergency Department Case Presentation of Congenital Lobar Emphysema

Kimberly L. Moulton, Andrea FangStanford University.United States CureusCureus 2021; 13: DOI: 10.7759/cureus.13814 AbstractCongenital lobar emphysema (CLE) and congenital pulmonary lymphangiectasis (CPL) are rare conditions that are most often identified with prenatal ultrasonography. Occasionally, this disease process is first identified in the emergency department (ED), where the physician should avoid common pitfalls in order to prevent acute

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Case Report: A Relatively Mild Presentation of Unilateral Congenital Pulmonary Lymphangiectasia

Dionne Adair, Raja Rabah, Maria Ladino-Torres, Thomas G. SabaCS Mott Children’s Hospital and Michigan Medicine.United States Frontiers in PediatricsFront Pediatr 2021; 9: DOI: 10.3389/fped.2021.657473 AbstractPulmonary lymphangiectasia (PL) is a rare congenital disorder of pulmonary lymphatic development. Although it was traditionally a fatal disorder of infancy, some cases in later childhood have been reported, suggesting a spectrum

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