ArticleRadiology case reports2024
Primary hepatic leiomyosarcoma with adrenal and hepatic metastasis: Case report and literature review.
Article in Radiology case reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Who cites it
3 citing papers in PubMed.
- Primary malignant peripheral nerve sheath tumor of the liver: a case report and literature review.Frontiers in oncology · 2026Article
- Primary hepatic leiomyosarcoma concurrent with early-stage lung adenocarcinoma: a rare case report.Frontiers in oncology · 2025Article
- Case report and literature review: primary hepatic leiomyosarcoma with misdiagnosis and SDHB positive expression.Frontiers in oncology · 2025Article
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Authors and funding
10 authors.
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Abstract
Primary hepatic leiomyosarcoma (PHL) is a rare malignant tumor, which originates from smooth muscles. The imaging features are nonspecific and the diagnosis is often delayed until the tumor reaches a large size, which leads often to a dismal prognosis. We report a case of a 46-year-old male patient who was complaining about abdominal pain for 2 months. The imaging revealed the presence of a large mass in the liver with adrenal and liver metastasis. Diagnosis of PHL was confirmed by histopathological and immunohistochemical examinations. In this case report, we review the epidemiological, clinical, and paraclinical aspects of the disease, as well as the treatment modalities.
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