Liver Mesenchymal Hamartoma

Liver Mesenchymal Hamartoma (LMH) is a rare benign lesion occurring primarily in the pediatric population. The pathogenesis is not certain, although an association has been seen with abnormal mesodermal synchronous development in the portal tract. A 4-year-old female patient, with no relevant person...

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Bibliographic Details
Published in:	Journal of pediatric surgery case reports Vol. 68; p. 101839
Main Authors:	Cahís Vela, Nuria, Loverdos Eseverri, Inés, Beltrán Salazar, Viviana Patricia, Brun Lozano, Nuria, Ferreres Piñas, Joan Carles, Hernández, Carlos José Ruiz
Format:	Journal Article
Language:	English
Published:	Elsevier Inc 01-05-2021 Elsevier
Online Access:	Get full text
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Summary:	Liver Mesenchymal Hamartoma (LMH) is a rare benign lesion occurring primarily in the pediatric population. The pathogenesis is not certain, although an association has been seen with abnormal mesodermal synchronous development in the portal tract. A 4-year-old female patient, with no relevant personal and family history, was evaluated for abdominal distension. Hepatomegaly was detected as a casual finding. Image tests showed a multiseptae cystic lesion in the right lobe of the liver. Gross pathological review of the lesion identified a cystic consistency tumor occupying the entire right lobe and displacing suprahepatic vessels, gallbladder and vascular pedicle. Complete dissection was performed. Histologically studies showed a smooth and shiny external surface, multiloculated, with a liquid content exit of yellowish coloration and thickened walls with areas of yellowish coloration and focally of increased consistency. The mass consisted on cystic neoplasm of thickened walls and abundant vessels, with calcified areas, as well as dilated biliary and lymphatic ducts and mild associated chronic inflammatory component. The patient was discharged home on postoperative day seven. A review of the literature for LMH in children reports a few publications, most of them limited to case reports. LMH has the potential for mixed pathology, multifocality, incomplete regression and rare malignant transformation, so it is important to make a correct differential diagnosis in order to not underdiagnose.
ISSN:	2213-5766 2213-5766
DOI:	10.1016/j.epsc.2021.101839