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Splenic torsion in the setting of polysplenia syndrome

open access: yesJournal of Pediatric Surgery Case Reports, 2021
Background: Polysplenia syndrome is a rare condition that occurs when polysplenia co-exists with various other congenital anomalies. Splenic torsion in the setting of polysplenia syndrome is extremely rare, having been documented only five times ...
Margaret Kennedy
exaly   +3 more sources

Polysplenia syndrome with complex heart disease and jejunal atresia with malrotation in neonate: A case report

open access: yesClinical Case Reports (discontinued), 2020
Polysplenia is heterotaxy syndrome or bilateral left‐sidedness. We report a case of polysplenia syndrome in order to draw attention to this rare syndrome that must be excluded in an infant presenting with congenital heart disease and intestinal ...
Adli Abdelrahim   +2 more
exaly   +2 more sources

Wandering spleen torsion in a patient with polysplenia syndrome

open access: yesRadiology Case Reports, 2022
Polysplenia Syndrome is a rare condition that refers to the presence of 2 or more spleens in association with other thoracoabdominal abnormalities.
Yazid Atatri
exaly   +3 more sources

Duplication of the spleen accompanied by multiple anomalies of the thorax and abdomen: a rare case [PDF]

open access: yesFolia Morphologica, 2020
Duplication of the spleen, classified as a polysplenia syndrome, is a very rare anomaly. Polysplenia is a complex syndrome with a broad spectrum of abnormalities. Other abnormalities accompanying polysplenia have been previously reported.
S. Sahin, A. H. Baykan
doaj   +2 more sources

Polysplenia syndrome with situs ambiguous, common mesentery, and IVC interruption discovered incidentally in an adult

open access: yesRadiology Case Reports, 2019
Polysplenia syndrome associates multiple spleens to other malformations, most frequently cardiac, vascular, visceral, and biliary malformations. Polysplenia has been described mainly in childhood owing to critical anatomic malformations related to ...
Hajar El Mortaji   +3 more
exaly   +3 more sources

A Rare Case of Heterotaxy Syndrome Associated with Hepatolithiasis and Pre-duodenal Portal Vein [PDF]

open access: yesJournal of Clinical and Diagnostic Research, 2017
Polysplenia syndrome is characterised by spectrum of abnormalities which are rarely diagnosed in adults as an incidental finding. The anomalies include multiple spleens, midline liver, gall bladder and biliary tract anomalies, short pancreas, agenesis ...
Varna Shetty   +2 more
doaj   +1 more source

An extremely rare case of congenitally absent superior mesenteric artery and polysplenia undergoing aneurysmectomy for superior mesenteric artery aneurysm

open access: yesAnnals of Vascular Surgery - Brief Reports and Innovations, 2023
We herein reported an extremely rare adult case with a congenitally absent superior mesenteric artery associated with polysplenia, who successfully underwent aneurysmectomy and revascularization for superior mesenteric artery aneurysm. To investigate the
Yoichi Kawahira   +3 more
doaj   +1 more source

Polysplenia and other anatomical variants of the spleen

open access: yesJournal of Education, Health and Sport, 2022
The anatomy, physiology and embryology of the spleen are essential fields of study for the determination of congenital varieties as well as the pathological processes occurring in this organ.The aim of this study is to summarize the current knowledge on
Agnieszka Kopystecka   +5 more
doaj   +1 more source

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

Heterotaxy pattern associated with sinus node dysfunction in an adult: A case report

open access: yesClinical Case Reports, 2023
Key Clinical Message A 26‐year‐old male patient admitted to the hospital ward with experience of repetitive syncopes for a year. The patient was diagnosed with sick sinus syndrome.
Naman Shah   +8 more
doaj   +1 more source

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