Biopsy-driven diagnosis in infants with cholestatic jaundice in Iran

Elham Talachian1, Ali Bidari1, Mitra Mehrazma1

  • 1Elham Talachian, Nahid Nick-khah, Department of Pediatric Gastroenterology, Ali Asghar Children's Hospital, Iran University of Medical Sciences, Tehran 1919816766, Iran.

Insights

Biliary atresia is the most common diagnosis in infants with cholestasis. Delays in liver biopsy for infantile cholestasis can worsen outcomes, especially for biliary atresia.

Area of Science:

  • Pediatric Gastroenterology
  • Hepatology
  • Diagnostic Pathology

Background:

  • Infantile cholestasis (IC) presents a diagnostic challenge in pediatric healthcare.
  • Accurate diagnosis through liver biopsy is crucial for timely intervention and management.
  • Understanding the etiological spectrum of IC is vital for public health initiatives in Iran.

Purpose of the Study:

  • To ascertain the frequency of various diagnoses confirmed by liver biopsy in infants presenting with cholestasis.
  • To analyze the common clinical findings and demographic data associated with infantile cholestasis.
  • To evaluate the time interval between symptom onset and liver biopsy in affected infants.

Main Methods:

  • Retrospective analysis of liver biopsy reports from children under two years with cholestatic jaundice.
  • Review of archived pathology blocks by a pathologist blinded to initial diagnoses.
  • Comparison with chart records to ensure diagnostic accuracy.
  • Collection of clinical and histological data using a structured checklist.

Main Results:

  • Biliary atresia (BA) was the most frequent diagnosis (58.2%), followed by intrahepatic bile duct paucity (10.9%) and metabolic diseases (10.9%).
  • Common clinical signs included acholic stool (60.0%) and hepatomegaly (54.5%).
  • A significant delay was observed between jaundice onset (mean 43.8 days) and liver biopsy (mean 102.0 days), particularly for BA.

Conclusions:

  • Biliary atresia is the predominant cause of infantile cholestasis requiring liver biopsy in this Iranian cohort.
  • The study highlights a critical delay in the diagnostic process for infantile cholestasis.
  • Prompt liver biopsy is essential to prevent irreversible liver damage in conditions like biliary atresia.
Abstract

Related Concept Videos

Jaundice01:25

Jaundice

Jaundice, or icterus, is the yellow discoloration of the skin, sclerae, and mucous membranes. It happens when plasma bilirubin levels rise above 2.5-3 mg/dL, leading to bilirubin deposition in tissue.Bilirubin is a byproduct of hemoglobin degradation. In macrophages, hemoglobin breaks down into globin and heme. Globin is converted into amino acids, while heme is turned into biliverdin by heme oxygenase, which is then reduced to unconjugated bilirubin by biliverdin reductase.Unconjugated...
35
Diseases of the Liver and Gallbladder01:26

Diseases of the Liver and Gallbladder

Liver and gallbladder diseases are a significant health concern, with prominent conditions including cirrhosis, hepatitis, non-alcoholic fatty liver disease (NAFLD), and gallstones. Jaundice is a common manifestation of liver and biliary disease.
Cirrhosis is characterized by the scarring of hepatic lobules in the liver, which are replaced by fibrous tissue, affecting the liver's normal functioning. NAFLD, on the other hand, is caused by an excessive build-up of fat in the liver, not...
2.1K
Cholecystitis01:20

Cholecystitis

Cholecystitis is inflammation of the gallbladder, most commonly caused by obstruction of the cystic duct. This blockage prevents bile from draining, leading to gallbladder distension, inflammation, and potentially serious complications. This condition may present acutely or chronically and can happen with or without gallstones.EtiologyAbout 95% of cholecystitis cases are calculous, caused by gallstones blocking the cystic duct, leading to bile accumulation and inflammation of the gallbladder...
29