Results 31 to 40 of about 1,594 (165)

Risk factors for Fontan-associated hepatocellular carcinoma.

open access: yesPLoS ONE, 2022
AimsThe incidence of hepatocellular carcinoma (HCC) in patients with Fontan-associated liver disease (i.e., FALD-HCC) has increased over time. However, the risk factors for HCC development remain unclear.
Tomomi Kogiso   +6 more
doaj   +1 more source

Thoracoscopic oesophago-oesophagostomy in the prone position for oesophageal stenosis caused by dilated azygos vein in polysplenia-associated heterotaxy

open access: yesJournal of Minimal Access Surgery, 2021
Background: Heterotaxy syndrome is associated with a plethora of cardiovascular and other multi-system anomalies with a high childhood mortality. A dilated azygos vein as part of the polysplenia variant of heterotaxy syndrome may cause oesophageal ...
Rajesh Bhojwani, Nikhil Jain
doaj   +1 more source

Polysplenia in an Adult Patient

open access: yesInternal Medicine, 2012
A 45-year-old woman was referred for CT of the abdomen due to endoscopically detected esophageal varices. The patient complained of dizziness and long-term epigastric pain. The CT scan showed five aberrant splenic nodules (Picture a), a short pancreas (Picture b, arrowhead), a preduodenal portal vein (Picture b, arrow), intestinal malrotation (Picture ...
Turkalj, Ivan   +3 more
openaire   +3 more sources

Splenic Torsion in Heterotaxy Syndrome with Left Isomerism: A Case Report and Literature Review

open access: yesDiagnostics, 2022
Splenic torsion is an unusual condition that results in congenital abnormality, especially in the visceral abnormal arrangement. We report the case of an 8.5-year-old boy with features in the right upper quadrant.
I Nok Cheang   +4 more
doaj   +1 more source

Infantile Bowel Obstruction in a Patient with Situs Inversus Totalis and Polysplenia: A Case Report

open access: yesInternational Medical Case Reports Journal, 2022
Abdullahi Yusuf Ali,1 Ahmet Biyikli,1 Abdishakur Mohamed Abdi,1 Ilkay Guler2 1Department of Pediatric Surgery, Somalia Turkish Training and Research Hospital, Mogadishu, Somalia; 2General Directorate of Public Hospitals, Ministry of Health of Republic of
Yusuf Ali A, Biyikli A, Abdi AM, Guler I
doaj  

BILIARY ATRESIA IS ASSOCIATED WITH POLYSPLENIA AND SITUS INVERSUS ON ULTRASOUND, A CASE REPORT STUDY.

open access: yesStudent's Journal of Health Research Africa, 2023
Biliary atresia is a destructive, idiopathic, and inflammatory cholangiopathy that affects intra and extra-hepatic bile ducts leading to fibrosis and obliteration of the biliary tract and development of liver cirrhosis.
Evalyne Tukwasibwe   +3 more
doaj   +1 more source

A CASE OF COR BILOCULARE ACCOMPANIED BY POLYSPLENIA [PDF]

open access: yesActa Medica Iranica, 1972
The clinical history and necroscopic fi ndings of a 3 -} year old girl - involved in cor biloculare was reported. In th is case dextrotransposition of the great a rteries and polysplenia was observed. The majority of cor biloculare cases appearing in the
M. S. ROJHAN
doaj   +2 more sources

Breaking patterns: Multiple spleens and the absent right kidney—A rare and unique case report in a 33-year-old burn victim

open access: yesRare
Polysplenia is a congenital condition characterized by the presence of multiple small accessory spleens with absent of primary spleen. While polysplenia may occur in isolation or may be present as part of Polysplenia syndrome.
Jayeshkumar Kanani   +1 more
doaj   +1 more source

Anatomy, embryology, and imaging of situs ambiguous with polysplenia and left IVC

open access: yesRadiology Case Reports, 2023
The situs ambiguous or heterotaxy syndrome is a type of syndrome that involves multiple visceral abnormalities, vascular ones and associated with left isomerism.
Rosa Montero-Macías, MD   +4 more
doaj   +1 more source

Clinical and Genetic Study of a Pseudo‐Dominant Primary Ciliary Dyskinesia Pedigree: The First DNAAF1‐Associated Family Reported in Chinese Population

open access: yesMolecular Genetics &Genomic Medicine, Volume 14, Issue 7, July 2026.
We report pseudo‐dominant PCD inheritance in a Chinese family due to novel DNAAF1 mutations. Affected members across two generations showed significant variability in lung disease progression and visceral arrangement. ABSTRACT Background Primary ciliary dyskinesia (PCD) is a rare, genetically heterogeneous disorder typically inherited in an autosomal ...
Zhuoyao Guo   +3 more
wiley   +1 more source

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