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Widespread haemorrhages in infants post-shunting (WHIPS): clinical features, risk factors and neuroimaging characteristics of a rare and under-recognised phenomenon.
Neuroradiology
October 2024
Department of Medical Imaging, Perth Children's Hospital, 15 Hospital Ave, Nedlands, WA, 6009, Australia.
Purpose: Infants undergoing CSF shunting procedures face a rare complication which we propose to rename "Widespread Haemorrhages in Infants Post-Shunting" (WHIPS) to better capture this unique phenomenon specific to infants undergoing CSF diversion. Our objective is to analyse the risk factors for WHIPS development and provide a detailed neuroradiological description of these haemorrhages.
Materials And Methods: A radiology information system (RIS) was searched using the search terms "shunt" and/or "catheter" and/or "drain" and/or "ventriculoperitoneal" and/or "VP" between September 2008 to January 2021 for patients < 12 months of age.
Congenital lung malformations: a nationwide survey on management aspects by the Italian Society of Pediatric Surgery.
Pediatr Surg Int
February 2024
Pediatric Thoracic and Airway Surgery, IRCCS Giannina Gaslini, Genoa, Italy.
Introduction: Over the years, congenital lung malformations (CLM) management remains a controversial topic in pediatric thoracic surgery. The Italian Society of Pediatric Surgery performed a national survey to study the current management variability among centers, trying to define national guidelines and a standardized approach of children with congenital lung malformations.
Methods: Following a National Society approval, an electronic survey including 35 items on post-natal management was designed, focusing on surgical, anesthesiology, radiology and pneumology aspects.
Rare presentation of a rare disease: Bilateral congenital lobar overinflation.
Radiol Case Rep
April 2024
Department of Radiology, Addis Ababa University, College of Health Sciences, Addis Ababa, Ethiopia.
Congenital lobar overinflation is a rare but well-recognized congenital cause of neonatal and infantile respiratory distress. At times, the condition can mimic other congenital or acquired diseases and have atypical distribution and imaging patterns. Lobectomy of the involved lobe(s) is curative.
View Article and Find Full Text PDFRare interstitial lung disease in a preterm neonate with congenital lobar emphysema.
BMJ Case Rep
November 2022
Paediatrics, Case Western Reserve University Hospital, Cleveland, Ohio, USA
Congenital lobar emphysema (CLE)/congenital alveolar overdistension/congenital lobar overinflation or infantile lobar emphysema is a rare developmental anomaly of the lower respiratory tract which is characterised by hyperinflation of one or more of the pulmonary lobes. Histopathology may be variable, which may show abnormality in the cartilage, granulation tissue, mucosal folds, etc. We report a rare underlying histopathology in a preterm neonate with CLE.
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