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Isolation of Neonatal Extrahepatic Cholangiocytes
Published on: June 5, 2014
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.
Aim:
To determine the frequencies of diagnoses confirmed by liver biopsy in infants with cholestasis in an Iranian pediatric hospital.
Methods:
This was a retrospective study conducted in a tertiary referral children's hospital in Iran. We retrieved all pathology reports of liver biopsies from children less than two years of age who had presented for evaluation of cholestatic jaundice from March 2001 to March 2011. Additional specimen samples obtained from archived pathology blocks were reviewed by a pathologist blinded to the final diagnosis. These results were compared with the pathology reports from chart records to ensure consensus and eliminate any inconsistencies in final diagnoses. A structured checklist was used to gather information on multiple variables including age, sex, gestational age at birth, birth weight, age at which hyperbilirubinemia manifested, presence and identification of associated anomalies, clinical manifestations, and histological findings from liver biopsies. The baseline data are reported using descriptive statistics, and differences between groups were assessed by Fisher's exact test and Student's t test when indicated.
Results:
Fifty-five cases (28 females; 27 males) of infantile cholestasis (IC) were included in this study. The mean serum total bilirubin and direct bilirubin at presentation were 13.6 ± 5.9 and 7.3 ± 3.4, respectively. Forty cases (72.7%) were the product of term pregnancies. Common associated clinical findings were acholic stool in 33 cases (60.0%), hepatomegaly in 30 cases (54.5%), and dark-colored urine in 21 cases (38.2%). Biliary atresia (BA) was the most frequent diagnosis, found in 32 cases (58.2%), followed by intrahepatic bile duct paucity found in 6 cases (10.9%), metabolic disease in 6 cases (10.9%), idiopathic neonatal hepatitis in 5 cases (9.1%), choledochal cyst in 2 cases (3.6%), liver cirrhosis in 2 cases (3.6%), and progressive familial intrahepatic cholestasis and portal fibrosis each in 1 case (1.8%). The mean times for jaundice onset and liver biopsy were 43.8 and 102.0 d, respectively. In BA, the mean age at jaundice presentation was 21 d and for liver biopsy was 87.5 d, representing a mean delay of 66.5 d.
Conclusion:
A significant delay was found between IC presentation and liver biopsy, which is detrimental in conditions that can cause irreversible liver damage, such as BA.
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