Primary Hepatic Leiomyosarcoma Presenting as a Multiloculated Cystic Mass: A Case Report and Review of Literature
Primary hepatic leiomyosarcoma (PHL) is a rare malignant mesenchymal tumor representing a small fraction of primary hepatic cancers. Due to its nonspecific clinical and radiologic presentation, it is often misdiagnosed. We present the case of an 82-year-old male who presented with altered mental status and was found to have a multiloculated cystic mass in the liver, initially suspected to be a hepatic abscess. Histopathological evaluation of the mass revealed a diagnosis of PHL. Despite palliative chemotherapy, the patient succumbed to metastatic disease within two months. PHL is a rare neoplasm with varied clinical manifestations. The unusual cystic presentation, as seen in this case, highlights the importance of maintaining a broad differential when evaluating hepatic masses.
Authors
- Satyapal Chahar (ORCID: https://orcid.org/0000-0002-0888-5347)
- Akhila Aravind (ORCID: https://orcid.org/0009-0003-0873-3727)
- Youssef Al Hmada
- Anita Choudhary
- Navdeep Kaur
Institutions
- Mayo Clinic (US)
- Jackson Memorial Hospital (US)
- University of Mississippi Medical Center (US)
- Mayo Clinic in Arizona (US)
- Dominion (United States) (US)
- Mayo Clinic in Florida (US)
Publication Details
- Journal
- Cureus
- Published
- 2025-12-23
- DOI
- https://doi.org/10.7759/cureus.99966
- Primary Topic
- Vascular Tumors and Angiosarcomas
- Type
- article
- Field-Weighted Citation Impact
- 0.00