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Updated: Feb 15, 2026

Full-Endoscopic Surgery for Hypothalamic Hamartoma Resection
Published on: April 12, 2024
Mesenchymal Hamartoma of the Liver: Complete Excision Always Necessary
Suman B Koganti1,2, Venu Madhav Thumma2, Bheerappa Nagari2
1Department of Surgery, BLHC, Icahn School of Medicine at Mount Sinai, New York, NY 10457, USA.
Abstract:
Mesenchymal hamartoma (MH) is not an uncommon tumor of the liver in the age group of 2-10 years. It is the second most common benign liver tumor in children. Previously considered a developmental anomaly, newer insights into other theories of origin including toxic-metabolic, ischemic, and a true neoplastic process are in progress. Previous understanding of a purely benign nature of the tumor is being overridden by a real malignant transformation. Complete excision of the tumor with clear margins is recommended to achieve a long term cure. A thorough understanding of the natural history of these tumors and skillful surgical treatment are indispensable elements of care.
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