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Aim: Mesenchymal hamartoma of the liver is an entity with a varied presentation and frequent initial delay in diagnosis. The macroscopic appearance too is quite heterogeneous with solid, cystic and mixed variants being present with varying degrees of vascularity. Management will depend on presentation and expertise available. We look at a single centre experience with the mesenchymal hamartomas.
Method: Retrospective patient record review of the past 30 years, 1976-2006.
Results: Seventeen patients aged 1 day to 15 years were identified, with a histopathological diagnosis of mesenchymal hamartoma of the liver. The anatomical location in the liver was 12 in the right liver and the 5 in the left. All patients presented with abdominal distension, eight had significant anorexia and or vomiting. Ultrasound scan was done in all patients. Findings were that of a mass and or cysts. The cysts were multiple in all cases but one and were interspersed with solid elements. Calcification was noted in only two of the patients. Operative approaches were six right hepatectomy, four wedge excision, seven tumour excisions by division of its pedicle; two of these were done laparoscopically, by cyst drainage and excision of the solid component. The tumours were all confirmed as mesenchymal hamartomas; size ranged from 412 to 2,230 g. Complications included three related to misdiagnosis (hydatid disease, and hepatoblastoma). Intraoperative problems consisted of preoperative bleeding resulting in an on-table hypovolaemic arrest and in a second case a bile duct injury. Postoperative problems consisted of an initial incomplete resection, with residual tumour on the IVC. There was rapid regrowth of tumour and death after a second exploration. Two children developed fluid collections requiring re-exploration and drainage. The surviving children have been followed up for a median time period of 4 months (range 1 month-11 years) and are well.
Conclusion: Although hamartomas of the liver are histologically benign, their clinical course and the complications of surgical treatment can be significant. They can often pose diagnostic dilemmas and may have a propensity for local recurrence and malignant degeneration.
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http://dx.doi.org/10.1007/s00383-008-2239-0 | DOI Listing |
World J Hepatol
August 2025
Department of Radiology, Aga Khan University, Karachi 74800, Sindh, Pakistan.
Pediatric liver masses encompass a diverse spectrum of benign and malignant lesions, with distinct patterns based on patient age. Optimal imaging is critical for timely diagnosis, management, and prognosis. This pictorial minireview categorizes pediatric liver masses by age group to guide hepatology and radiology practice, with an emphasis on imaging characteristics.
View Article and Find Full Text PDFBMJ Case Rep
August 2025
Neonatology, AIIMS Nagpur, Nagpur, Maharashtra, India
Congenital hepatic haemangioma is a rare benign vascular tumour in neonates. This case describes a neonate with an antenatally detected abdominal mass, suspected to be a hepatic neoplasm. Postnatal imaging revealed a large hepatic lesion with diagnostic uncertainty between hepatic haemangioma, hepatoblastoma and mesenchymal hamartoma.
View Article and Find Full Text PDFS D Med
August 2025
Department of Obstetrics and Gynecology, University of South Dakota Sanford School of Medicine.
Placental mesenchymal dysplasia (PMD) and hepatic mesenchymal hamartomas are rare diseases associated with Beckwith-Wiedemann Syndrome (BWS). We present the case of a 22-year-old diagnosed with PMD at 24 weeks gestation who required emergent delivery secondary to fetal distress and preeclampsia at 30 weeks' gestation. The neonate was diagnosed with a hepatic mesenchymal hamartoma following delivery.
View Article and Find Full Text PDFAm J Dermatopathol
July 2025
Yosemite Pathology Medical Group, Modesto, CA.
Background: Cutaneous hamartomas are benign lesions composed of disorganized but mature tissue elements normally found at the site. Although many types are well defined, some rare variants do not conform to established categories.
Case Presentation: We present a unique case of a cutaneous hamartoma with prominent mesenchymal overgrowth and minimal epithelial and adnexal components.
Surg Pathol Clin
September 2025
Department of Pathology and Laboratory Medicine, Dartmouth Hitchcock Medical Center, Lebanon, NH 03756, USA; Geisel School of Medicine at Dartmouth, Hanover, NH 03755, USA. Electronic address:
Head and neck bone tumors carry unique clinical, imaging, morphologic, and prognostic features compared to their peripheral counterparts and warrant a multidisciplinary approach for optimizing diagnosis and patient care. This review explores tumors characteristic of the head and neck (nasal chondromesenchymal hamartoma and osteochondromyxoma), as well as those that occur in other sites but have distinct features in this region (conventional and mesenchymal chondrosarcoma, osteosarcoma, and chordoma). Embryologic development and anatomic complexity of this region affect diagnostic considerations and patient management.
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