Results 1 to 10 of about 1,338 (153)

Splenic Infarct with Polysplenia Syndrome [PDF]

Journal of the Belgian Society of Radiology, 2022
A rare case of spontaneous splenic infarction with polysplenia is presented. The diagnosis was made by confirmed by enhanced computed tomography (CT), which showed multiple spleens in the left abdomen and one of the spleen showing low attenuation areas ...
Qin Ling Zhu, Wenjun Zhu
doaj   +5 more sources

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

Clinical Case Reports, 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 ...
Roya Arif Huseynova, Latifa A. Bin Mahmoud, Adli Abdelrahim, Majeed A. Alroiedy, Ogtay Huseynov   +4 more
doaj   +3 more sources

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

Radiology 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, Kenza Elatiqi, Hanane El Hammaoui, Soumaya Alj   +3 more
doaj   +4 more sources

Polysplenia syndrome in adulthood: A case report of incidental discovery [PDF]

Radiology Case Reports
The Polysplenia Syndrome (PSS) is a form of heterotaxy, a rare congenital anomaly with an estimated incidence of 1 in 250,000 live births, first described by Helwig in 1929.
Jihane El Houssni, Sanae Jellal, Ismail Neftah, Fariss Dehayni, Siham El Haddad, Nazik Allali, Latifa Chat   +6 more
doaj   +4 more sources

Polysplenia syndrome associated with multisystem malformation: A rare case report [PDF]

Radiology Case Reports
Polysplenia syndrome is a rare congenital disease with multiple systemic developmental abnormalities. Their occurrence and development are closely related to embryonic development. The prognosis of the disease depends on its anatomical structure, and the
Wangyi Yang, Yaqi He, Zhaocheng Kuang, Wenyan Guo   +3 more
doaj   +4 more sources

Splenic torsion in the setting of polysplenia syndrome

Journal 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, Daniel Farinas Lugo, William Raleigh Thompson   +2 more
doaj   +3 more sources

Wandering spleen torsion in a patient with polysplenia syndrome [PDF]

Radiology 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.
Muath Draghmeh, Ameed Taher, MD, Yazid Atatri, MD, Fadi Abu Al-rub, MD, Walid Muhaisen, MD, Obada Khanfar, MD   +5 more
doaj   +2 more sources

Polysplenia syndrome complicated with posterior nutcracker syndrome

Asian Journal of Surgery, 2023
Binglin Lai, Junyuan Zhong, Jianping Zhong   +2 more
doaj   +5 more sources

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

Journal 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, Samir Mustaffa Paruthikunnan, Sachin Gullappa Shatagar   +2 more
doaj   +1 more source

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

Folia 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   +1 more source