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Polysplenia syndrome complicated by multiple intrahepatic bile duct stones in an adult: a case report [PDF]

Frontiers in Medicine
Polysplenia syndrome is a rare congenital disorder characterized by multiple spleens and complex visceral and vascular anomalies. We report an adult case admitted for multiple intrahepatic bile duct stones.
Jiahao Zhang, Jiliang Lu, Hongzhong Liang, Pengyu Chen, Zheng Wang, Naiqing Liu, Jinghua Liu, Jinghua Liu   +7 more
doaj   +2 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
exaly   +3 more sources

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

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   +3 more sources

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

Clinical 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 ...
RoyA Huseynova, Oqtay Huseynov
exaly   +2 more sources

Wandering spleen torsion in a patient with polysplenia syndrome

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
exaly   +3 more sources

Heterotaxy polysplenia syndrome with cholangiopancreatic cancer: a case report and literature review [PDF]

Frontiers in Medicine
BackgroundHeterotaxy polysplenia syndrome is a rare condition characterized by multiple abnormal spleens and irregular placement of various organs. Some patients have been documented as developing various types of cancers, although the association with ...
Ziye Chen, Ziye Chen, Yu-Ann Chen, Yu-Ann Chen, Xuedong Wang, Wenyan Song, Wenyan Song, Yadi Geng, Yadi Geng, Pengfei Wang, Siming Kong, Jiahong Dong, Jiahong Dong, Hui Bai, Yunfang Wang, Yunfang Wang, Yunfang Wang, Yunfang Wang   +17 more
doaj   +2 more sources

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

Radiology 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, Mohamed Abdellaoui, MD, Meriem Edderai, MD, Rachida Saouab, MD, Hassan Ennouali, MD, Jamal El Fenni, MD, Ouijdane Zamani, MD   +6 more
doaj   +2 more sources

Incidental Detection of Adult Polysplenia Syndrome With Situs Inversus Totalis, Interrupted Inferior Vena Cava, and Bronchiectasis [PDF]

Methodist DeBakey Cardiovascular Journal
Incidental detection of polysplenia associated with situs inversus totalis in an adult is rarely reported in literature.1,2 “Heterotaxy” refers to a wide spectrum of anomalies involving dysmorphism of thoracoabdominal organs across the right-left axis of
Kanupriya Arora, Mansi Verma, Sushma Makhaik   +2 more
doaj   +2 more sources

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

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
exaly   +3 more sources

From multiple spleens to absence: Insights from two cases of heterotaxy syndromes [PDF]

Radiology Case Reports
Heterotaxy syndrome is a rare congenital disorder characterized by abnormal arrangement of the thoracic and abdominal organs and is classified into polysplenia (left isomerism) and asplenia (right isomerism) syndromes.
Suman Paudel, MD, Rishi Ram Banjade, MBBS, Niraj Kumar Sharma, MD, Sharmila Ghimire, MD, Prerana Singh Rokaha, MBBS   +4 more
doaj   +2 more sources