Paediatric sickle cell disease presenting with hepatobiliary symptoms—a case presentation and brief literature review

Autor: Aditi Kumar, Rashmi Ranjan Behera, Samarendra Mahapatro, Ranjan Patel, Hemanta Nayak, Amit Kumar Satapathy

Publikováno v: Egyptian Pediatric Association Gazette, Vol 72, Iss 1, Pp 1-5 (2024)

Abstract Background Sickle hepatopathy is the hepatobiliary dysfunction associated with sickle cell disease. It has a varied spectrum ranging from asymptomatic transaminasemia to gallstones or fulminant liver failure. Hepatobiliary manifestations may

Externí odkaz: https://doaj.org/article/530e5bd942aa40918478c99209cfdb94

Acute and chronic hepatobiliary manifestations of sickle cell disease: A review.

Autor: Shah R; Rushikesh Shah, Saurabh Chawla, Division of Digestive Diseases, Department of Internal Medicine, Emory University School of Medicine, Atlanta, GA 30322, United States., Taborda C; Rushikesh Shah, Saurabh Chawla, Division of Digestive Diseases, Department of Internal Medicine, Emory University School of Medicine, Atlanta, GA 30322, United States., Chawla S; Rushikesh Shah, Saurabh Chawla, Division of Digestive Diseases, Department of Internal Medicine, Emory University School of Medicine, Atlanta, GA 30322, United States.

Publikováno v: World journal of gastrointestinal pathophysiology [World J Gastrointest Pathophysiol] 2017 Aug 15; Vol. 8 (3), pp. 108-116.