A case demonstrates diagnostic challenges of mesenchymal hamartoma resembling hepatic tumors in a young adult.
Mesenchymal hamartoma of the liver (MHL) is a rare benign lesion usually seen in infants and young children; adult onset is exceptional and can mimic a broad spectrum of hepatic neoplasms on imaging, including hepatocellular, cholangiocytic/biliary, and mesenchymal tumors. A 31-year-old woman was found to have a 23-mm hyperechoic mass in segment 7 on screening ultrasonography. One year later, it had enlarged to 68 mm. Contrast-enhanced computed tomography showed a well-circumscribed 75-mm lesion with gradual heterogeneous enhancement. Given her >10-year history of oral contraceptive use, a benign hepatocellular tumor such as hepatocellular adenoma was suspected; however, biliary epithelial tumors and mesenchymal tumors were also considered in the differential diagnosis. Because of rapid growth and proximity to the right hepatic vein, robot-assisted extended posterior sectionectomy with right hepatic vein resection was performed. Pathology revealed fibromyxoid stroma with spindle mesenchymal cells, irregular bile ducts, consistent with MHL without malignant change.
No takes yet. Share an insight, caveat, or question.
Saruta et al. (2026) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: