ArticleJournal of clinical and experimental hepatology2018
Primary Hepatic Leiomyosarcoma: Histopathologist's Perspective of a Rare Case.
Article in Journal of clinical and experimental hepatology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.
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Who cites it
11 citing papers in PubMed.
- Article
- Primary hepatic leiomyosarcoma diagnosed after right hepatectomy: A rare case report.Rare tumors · 2026Article
- Primary hepatic leiomyosarcoma concurrent with early-stage lung adenocarcinoma: a rare case report.Frontiers in oncology · 2025Article
- Primary hepatic leiomyosarcoma masquerading as liver abscess: A case report.World journal of gastrointestinal surgery · 2024Article
- Imaging findings of primary hepatic leiomyosarcoma: a case report and literature review.Frontiers in oncology · 2024Article
- Primary hepatic leiomyosarcoma: A case report and literature review.World journal of hepatology · 2022Article
- Large surgically resected leiomyosarcoma of the liver: a case report.Surgical case reports · 2020Article
- Case of primary hepatic leiomyosarcoma successfully treated with laparoscopic right hepatectomy.BMJ case reports · 2020Article
- Hepatic pleomorphic leiomyosarcoma after surgery for gastric gastrointestinal stromal tumor: a case report.Surgical case reports · 2019Article
- Clinical, Histopathological, and Immunophenotypic Spectrum of Hepatic Epithelioid Hemangioendothelioma: Eight Years' Data of a Tertiary Care Center from North India.Journal of clinical and experimental hepatologyArticle
- Hepatic Follicular Dendritic Cell Sarcoma with Epithelioid Morphology: Histopathologist's Perspective.Journal of clinical and experimental hepatologyArticle
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Authors and funding
5 authors.
Funding
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Abstract
Primary hepatic leiomyosarcoma is a rare primary mesenchymal tumor of the liver requiring exclusion of any other primary site of origin and histological and immunohistochemical exclusion of other hepatic/extrahepatic tumors with spindle cell morphology. Only about 70 cases are reported in the English literature and many of these tumors have predisposing conditions in the form of immunosuppression or associated malignancies. The occurrence of this tumor in the immunocompetent individual is also known. Histomorphology of this tumor shows a spindle cell lesion which needs to be distinguished from other spindle cell lesions of this region. The main diagnostic challenge of this tumor lies in its rarity, lack of awareness and morphological mimickers in the given site. A complete range of immunohistochemical markers is required to distinguish the lesion from its close morphological mimickers. Here, we discuss a case of primary hepatic leiomyosarcoma in an adult female patient with detailed histomorphological differentials and respective immunoprofiles.
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