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Porta hepatis lymphnode mimicking biliary atresia: A case report.

Authors :
Ngowi, Elisamia
Kwayu, Juliana
Kitua, Abduel
Ebrahim, Mohamedraza
Mwamanenge, Naomi
Abdallah, Yaser
Source :
International Journal of Surgery Case Reports; Sep2024, Vol. 122, pN.PAG-N.PAG, 1p
Publication Year :
2024

Abstract

Cholestasis is the impairment of normal bile flow causing accumulation of bile salts, lipids, and bilirubin in blood which presents as Jaundice. Jaundice beyond 2 weeks of age is rare in infancy with worldwide incidence of 1 in 2500 live births. Biliary atresia is the most common extra hepatic cause of cholestasis in late neonatal and infancy period. Cholestasis and hyperbilirubinemia cause irreversible brain and liver damage if not diagnosed and treated early. A 3-week-old neonate presenting with progressive yellowish discoloration of eyes and skin. Explorative laparotomy found anatomically normal liver and biliary tree, but a lymph node obstructing the common bile duct. This case was particularly unique as history of illness and initial investigations were suggestive of biliary atresia. However, the patient had lymph nodes with no history of any triggers to lymphadenopathy. It is a rare case of obstruction of biliary flow in this age group. Despite biliary atresia being the commonest cause of obstructive jaundice in infancy, it is important to rule out other causes like lymph nodes obstructing the biliary tree. • Cholestatic jaundice is rare in infancy and biliary atresia should be ruled out promptly as the most common cause. • It is important to do biopsy before exploratory laparotomy to minimize unnecessary surgical procedures. • Intrahepatic lymph node can mimic biliary atresia. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
22102612
Volume :
122
Database :
Supplemental Index
Journal :
International Journal of Surgery Case Reports
Publication Type :
Academic Journal
Accession number :
179463351
Full Text :
https://doi.org/10.1016/j.ijscr.2024.110040