Results 21 to 30 of about 1,525 (102)
Pancreatic Pseudocyst With Thoracic Extension: A Clinicoradiological Case Report
CECT sagittal view shows an enlarged, heterogeneously enhancing pancreas with a peripancreatic collection extending into the posterior mediastinum and compressing the esophagus with massive right pleural fluid noted. ABSTRACT Pancreatic pseudocysts are encapsulated, enzyme‐rich peripancreatic fluid collections that typically develop following acute or ...
Sachchu Thapa +7 more
wiley +1 more source
Introduction Nonimmune hydrops fetalis (NIHF) has numerous etiologies, the most common of which are cardiac anomalies and fetal infection. However, genetic disorders are also being increasingly recognized as a cause of NIHF. Here, we report a case of a neonate presenting with polyhydramnios, NIHF, structural heart disease, and diaphragmatic defect who ...
Rameshwar Prasad +5 more
wiley +1 more source
Bochdalek hernia (BH) is a rare paediatric condition, but late diagnoses occur in adults. It occurs following incomplete posterolateral development of the diaphragm. Adult BH is asymptomatic in most cases, but it has the potential of being life‐threatening.
Walter Abila Akello +4 more
wiley +1 more source
Abdominal wall surgery is emerging as a new subspecialty with reconstructive operations becoming increasingly complex. Central to any surgical subspecialty is comprehensive anatomical knowledge, which can be enhanced by cadaver dissection. An expert panel convened to develop a consensus framework highlighting key anatomical concepts and operative steps
Lawrence Nip +12 more
wiley +1 more source
ABSTRACT Aim Congenital diaphragmatic hernia (CDH) is a severe malformation with high morbidity and mortality. This Danish study evaluated the birth prevalence, co‐occurring malformations, and temporal trends of CDH over nearly three decades. Methods Nationwide data from the Danish Biobank Register were used to identify liveborn infants diagnosed with ...
Ulrik Lausten‐Thomsen +6 more
wiley +1 more source
Schematic depiction of congenital diaphragmatic hernia with abdominal organs displaced into the chest, accompanied by visual elements illustrating the key complications observed in this case: cardiac tamponade and pleural effusion. Created in BioRender. Davoodi Karsalari, P. (2025) https://BioRender.com/n8wws0e.
Pershia Davoodi Karsalari +6 more
wiley +1 more source
Ocular Findings as the Most Striking Manifestation of a SMAD3 Variant
ABSTRACT Loeys‐Dietz syndrome (LDS) is a heritable connective tissue disorder with variable expressivity. It is a multisystemic condition mainly characterized by a propensity for arterial aneurysms and dissections, skeletal manifestations, hypertelorism, bifid uvula, craniosynostosis, and cutaneous features.
Noémie Villeneuve‐Cloutier +7 more
wiley +1 more source
Impact of fetal treatments for congenital diaphragmatic hernia on lung development
Abstract The extent of lung hypoplasia impacts the survival and severity of morbidities associated with congenital diaphragmatic hernia (CDH). The alveoli of CDH infants and in experimental models of CDH have thickened septa with fewer type II pneumocytes and capillaries. Fetal treatments of CDH‐risk preterm birth.
Mar Janna Dahl +5 more
wiley +1 more source
Mesenchymal retinoic acid signaling is required for normal diaphragm development in mice
Single‐cell sequencing analysis of mouse pleuroperitoneal folds shows that genes associated with congenital diaphragmatic hernia and retinoic acid signaling are primarily expressed in the non‐muscular mesenchyme of the developing diaphragm. Blocking mesenchymal retinoic acid signaling in the developing diaphragm of Prrx1Cre:RARdn mice causes congenital
Juan F. Garcia Rivas +5 more
wiley +1 more source
Extrinsic heart compression by gastrointestinal (GI) structures is an often underrecognized finding in clinical practice. It is potentially related to unpredictable clinical conditions, ranging from incidental detection in asymptomatic subjects, to deranging and potentially life‐threatening clinical manifestations.
Riccardo Scagliola +3 more
wiley +1 more source

