Results 11 to 20 of about 1,222,131 (133)

Polysplenia syndrome with semi-annular pancreas, midgut malrotation and interrupted inferior vena cava: A rare adult case report [PDF]

open access: yesRadiology Case Reports
Polysplenia syndrome is a rare congenital anomaly within the heterotaxy spectrum. It is typically diagnosed in childhood due to associated cardiac malformations, whereas detection in adults without cardiovascular involvement is uncommon.
Saber Abdellah Bassel, MD   +6 more
doaj   +3 more sources

Polysplenia syndrome with duodenal and pancreatic dysplasia in a Holstein calf: a case report [PDF]

open access: yesBMC Veterinary Research, 2017
Background Laterality disorders of the abdominal organs include situs inversus totalis that mirrors the arrangements of all internal organs and heterotaxy syndrome (situs ambiguus) in which the thoracic or abdominal organs are abnormally arranged ...
Daisuke Kondoh   +8 more
doaj   +6 more sources

Acute splenic torsion in an adolescent with polysplenia syndrome: case report [PDF]

open access: yesItalian Journal of Pediatrics
Background Splenic torsion is a rare but potentially serious event. It can occur in association with various anatomical anomalies, such as polysplenia.
Flora Vassallo   +7 more
doaj   +3 more sources

Pediatric split liver transplantation in a patient with biliary atresia polysplenia syndrome and agenesis of inferior vena cava [PDF]

open access: yesKorean Journal of Transplantation, 2020
Biliary atresia (BA)-polysplenia syndrome (PS) is diagnosed in a small proportion of BA patients. We present a case of split liver transplantation (LT) successfully performed in a pediatric recipient with BA-PS.
Jung-Man Namgoong   +7 more
doaj   +3 more sources

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   +2 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

A Rare Case of Polysplenia Syndrome Associated with Severe Cardiac Malformations and Congenital Alveolar Dysplasia in a One-Month-Old Infant: A Complete Macroscopic and Histopathologic Study [PDF]

open access: yesJournal of Cardiovascular Development and Disease, 2022
Polysplenia syndrome represents a type of left atrial isomerism characterized by multiple small spleens, often associated with cardiac malformations and with situs ambiguus of the abdominal organs.
Cosmin Ioan Mohor   +13 more
doaj   +2 more sources

Congenital lobar emphysema associated with polysplenia syndrome [PDF]

open access: yesAnnals of Saudi Medicine, 2010
Polysplenia, or left isomerism, is a rare heterotaxy syndrome characterized by bilateral bi-lobed lungs, bilateral pulmonary atria, a symmetrical midline liver, and multiple aberrant splenic nodules.
Choh Naseer   +3 more
doaj   +2 more sources

Persistent Mullerian Duct Syndrome with Polysplenia and Short Pancreas: A Case Report [PDF]

open access: yesJournal of Nepal Medical Association, 2019
Persistent Mullerian duct syndrome is a rare entity and usually presents with common symptoms of undescended testis and hernia. The syndrome is caused by an insufficient amount of Mullerian inhibiting substance or due to the insensitivity of the target ...
Umesh Kumar Sharma   +3 more
doaj   +2 more sources

Ivemark syndrome: asplenia with kidney collecting duct cysts and polysplenia with cerebellar cyst

open access: yesThe Turkish Journal of Pediatrics, 2000
Two newborns, one male and one female, from two different families, with Ivemark syndrome proven at autopsy are reported. One of them had asplenia and another had polysplenia.
V Krźelj   +5 more
doaj   +3 more sources

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