Radiology Case Reports (Nov 2024)

Primary hepatic leiomyosarcoma with adrenal and hepatic metastasis: Case report and literature review

  • Chaymae Faraj, MD,
  • Youssef Mahdi, PhD,
  • Sara Essetti, MD,
  • Fatima Chait, MD,
  • Hatim Essaber, MD,
  • Asaad El Bakkari, MD,
  • Youssef Omor, PhD,
  • Rachida Latib, PhD,
  • Sanae Amalik, PhD,
  • Basma El Khannoussi, PhD

Journal volume & issue
Vol. 19, no. 11
pp. 4950 – 4954

Abstract

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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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