Results 1 to 10 of about 2,415 (196)

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   +4 more sources

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

open access: yesFrontiers 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   +7 more
doaj   +2 more sources

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

open access: yesFrontiers 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   +17 more
doaj   +2 more sources

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

open access: yesMethodist 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   +2 more
doaj   +2 more sources

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   +2 more sources

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

open access: yesRadiology 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   +4 more
doaj   +2 more sources

Splenic Infarct with Polysplenia Syndrome

open access: yesJournal 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   +4 more sources

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

open access: yesRadiology 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   +6 more
doaj   +2 more sources

Exploring the Differential Diagnosis of Adrenal Adenoma in the Context of Situs Ambiguous: A Clinical Case Study [PDF]

open access: yesMedicina
Situs anomalies, including situs inversus and situs ambiguous (SAMB), are rare congenital conditions typically noted in pediatric populations, with SAMB being particularly uncommon in adults.
Pavel E. Stanchev   +3 more
doaj   +2 more sources

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

open access: yesRadiology 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   +3 more
doaj   +2 more sources

Home - About - Disclaimer - Privacy