Resumo

FRAGA, João et al. Hepatic Myxoid Leiomyoma: A Very Rare Tumor. GE Port J Gastroenterol [online]. 2020, vol.27, n.5, pp.352-355. ISSN 2341-4545.  https://doi.org/10.1159/000504762.

Introduction: Mesenchymal tumors of the liver are rare, and in this group, myxoid leiomyomas are even rarer. So far, only 2 cases have been reported in the literature. Case Presentation: We aim to report the case of a 16-year-old female with a large lesion on the right hepatic lobe, grossly composed of gelatinous and heterogeneous tissue. Discussion: Histological evaluation revealed a benign mesenchymal neoplasm with expansive growth, paucicellular, with monotonous and dispersed spindle and ovoid cells, positive for α-smooth actin and h-caldesmon, without atypia or mitoses, consistent with the diagnosis of primary myxoid leiomyoma.

Palavras-chave : Myxoid leiomyoma; Liver; Mesenchymal tumor.

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