دورية أكاديمية

BILIARY ATRESIA IS ASSOCIATED WITH POLYSPLENIA AND SITUS INVERSUS ON ULTRASOUND, A CASE REPORT STUDY.

التفاصيل البيبلوغرافية
العنوان: BILIARY ATRESIA IS ASSOCIATED WITH POLYSPLENIA AND SITUS INVERSUS ON ULTRASOUND, A CASE REPORT STUDY.
المؤلفون: Evalyne Tukwasibwe, Richard Malumba, Racheal Ankunda, Mary Kaakyo
المصدر: Student's Journal of Health Research Africa, Vol 4, Iss 6 (2023)
بيانات النشر: Student's Journal of Health Research, 2023.
سنة النشر: 2023
المجموعة: LCC:General works
LCC:Infectious and parasitic diseases
LCC:Surgery
LCC:Public aspects of medicine
مصطلحات موضوعية: Ultrasound, Biliary atresia, Polysplenia, situs inversus, General works, R5-130.5, Infectious and parasitic diseases, RC109-216, Surgery, RD1-811, Public aspects of medicine, RA1-1270
الوصف: 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. The polysplenia syndrome is the most common anomaly, being found among patients with atresia, and is characterized by polysplenia/asplenia associated with a midline liver, interruption of the inferior vena cava, preduodenal portal vein, situs inversus and/or intestinal malrotation. Biliary atresia has an incidence of 1 in 10,000-15,000 live births and is more common in females than males. I report a case of a 5 months old baby boy who presented with yellow eyes since birth and abdominal distension for one week. The diagnosis of Biliary atresia, polysplenia, and situs inversus is usually based on clinical findings. Ultrasonography and Intraoperative cholangiogram are useful tools. The most suitable recommendable treatment for this specific case is surgery. This case study is to fill the knowledge gap among sonographers/radiographers regarding the existence of such cases to guide the management of those conditions, especially among infants.
نوع الوثيقة: article
وصف الملف: electronic resource
اللغة: English
تدمد: 2709-9997
Relation: https://sjhresearchafrica.org/index.php/public-html/article/view/338; https://doaj.org/toc/2709-9997
DOI: 10.51168/sjhrafrica.v4i6.338
URL الوصول: https://doaj.org/article/59dc6549448d4af2a4826ea4cba08a82
رقم الأكسشن: edsdoj.59dc6549448d4af2a4826ea4cba08a82
قاعدة البيانات: Directory of Open Access Journals
الوصف
تدمد:27099997
DOI:10.51168/sjhrafrica.v4i6.338