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Solid mesenchymal hamartoma in an adult: a case report
J C Hernández1, C Alfonso, L González
1Transplant Service, CIMEQ's Hospital, Havana, Cuba.
Journal of Clinical Pathology
|April 29, 2006
Summary
Mesenchymal hamartoma of the liver (MHL), a rare childhood tumor, can occur in adults. This case highlights MHL in a 51-year-old man, necessitating liver transplantation due to its solid mass presentation.
Area of Science:
- Hepatobiliary Medicine
- Surgical Pathology
- Pediatric Oncology (rare adult presentation)
Background:
- Mesenchymal hamartoma of the liver (MHL) is a rare liver tumor characterized by abnormal bile ducts within a myxoid stroma.
- While predominantly diagnosed in children, MHL can uncommonly present in adults, posing diagnostic and therapeutic challenges.
- Adult MHL cases are exceptionally rare, with limited literature available for guidance.
Observation:
- This report details a case of a 51-year-old male presenting with a large, completely solid liver mass in the right lobe.
- Preoperative imaging and biopsy revealed features suggestive of MHL, including a dense fibrous stroma with hyalinization and bile ducts.
Findings:
- Surgical excision was not feasible due to the mass's characteristics.
- The patient underwent liver transplantation, and definitive pathology confirmed the diagnosis of MHL.
- This represents the fourth reported case of MHL managed with liver transplantation in the literature.
Implications:
- The case underscores the importance of considering MHL in adult liver masses, even when rare.
- Liver transplantation is a viable, albeit uncommon, treatment option for adult MHL when resection is not possible.
- Further research into adult MHL presentation and management may improve diagnostic accuracy and treatment strategies.