Results 11 to 20 of about 1,937 (189)

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

Clinical 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, Sankalp Acharya, Apoorva Tripathi, Himanshi Bisht, Maitri Shah, Aayushi Pareek, Asmita Gera, Abhigan Babu Shrestha, Vikash Jaiswal   +8 more
doaj   +2 more sources

Polysplenia Syndrome With Persistent Left Superior Vena Cava: Case Report and Review of the Literature [PDF]

Global Pediatric Health, 2022
Polysplenia syndrome is an uncommon condition associating several splenic nodules (sometimes polylobed spleen and cases of normal spleen have been described) with a number of malformations that appear between the fourth and sixth week of embryonic ...
El Houss Salma MD, Amsiguine Najwa MD, Tantaoui Mehdi MD, Allali Nazik PhD, Chat Latifa PhD, El Haddad Siham PhD   +5 more
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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
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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

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   +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]

Journal 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, Sorin Radu Fleaca, Alexandra Oprinca Muja, George Calin Oprinca, Mihai Dan Roman, Radu Chicea, Adrian Gheorghe Boicean, Horatiu Dura, Ciprian Tanasescu, Nicolas Catalin Ionut Ion, Mihai Faur, Ciprian Ionut Bacila, Florina Batar, Calin Ilie Mohor   +13 more
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Polysplenia Syndrome and the Development of Heart Failure due to Associated Congenital Heart Defect [PDF]

Journal of the Belgian Society of Radiology
Key message: Patients with polysplenia syndrome can develop pulmonary hypertension and heart failure due to underlying congenital heart disease, underscoring the need for early recognition and intervention to prevent further progression of the condition.
Valerie Van Ballaer, Pieter Meersman, Nico Hustings   +2 more
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BILIARY ATRESIA IS ASSOCIATED WITH POLYSPLENIA AND SITUS INVERSUS ON ULTRASOUND, A CASE REPORT STUDY. [PDF]

Student's Journal of Health Research Africa, 2023
Biliary atresia is a destructive, idiopathic, and inflammatory cholangiopathy that affects intra and extra-hepatic bile ducts leading to fibrosis and obliteration of the biliary tract and development of liver cirrhosis.
Evalyne Tukwasibwe, Richard Malumba, Racheal Ankunda, Mary Kaakyo   +3 more
doaj   +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

Intra-Abdominal Abnormalities Associated with Polysplenia Syndrome [PDF]

Journal of the Belgian Society of Radiology, 2019
What to look for in case of polysplenia and/or unusual disposition of several intra-abdominal organs.
Hadrien Renier
doaj   +2 more sources