Pediatric Hepatocellular Adenomas: What Is Known and What Is New?

Abstract

Current understanding and classification of pediatric hepatocellular adenomas (HCA) are largely based on adult data. HCAs are rare in children and, unlike in adults, are often seen in the context of syndromes or abnormal background liver. Attempts to apply the adult classification to pediatric tumors have led to several “unclassifiable” lesions. Although typically considered benign, few can show atypical features and those with beta-catenin mutations have a risk for malignant transformation. Small lesions can be monitored while larger (>5.0 cm) lesions are excised due to symptoms or risk of bleeding/rupture, etc. Management depends on gender, age, underlying liver disease, multifocality, size of lesion, histologic subtype and presence of mutation, if any. In this review, we summarize the data on pediatric HCAs and highlight our experience with their diagnosis and management.

Update on the Pathology of Pediatric Liver Tumors: A Pictorial Review

“…Macroscopically, HA appears as a well-demarcated lesion with thin or no fibrous capsule [135]. Histologically, it shows thin liver cell plates composed of normal-sized hepatocytes along with numerous arteries unaccompanied by bile ducts or a portal vein.…”