| Literature DB >> 30302051 |
Suvradeep Mitra1, Sahaj Rathi2, Uma Debi3, Radha K Dhiman4, Ashim Das5.
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.Entities:
Keywords: AFP, Alpha Fetoprotein; CEA, Carcinoembryonic Antigen; CEMRI, Contrast Enhanced Magnetic Resonance Imaging; EBER-ISH; EBER-ISH, Epstein Barr Encoded RNA-In Situ Hybridization; EBV, Epstein-Barr Virus; FDG, Fluorodeoxyglucose; FNAC, Fine Needle Aspiration Cytology; GIST, Gastrointestinal Stromal Tumor; PET-CT, Positron Emission Tomography – Computed Tomography; SMA; SMA, Smooth Muscle Antigen; TPCT, Triple Phasic Computed Tomography; UGIE, Upper Gastrointestinal Endoscopy; USG, Ultrasonography; gastrointestinal stromal tumor; immunocompetent; primary hepatic leiomyosarcoma
Year: 2018 PMID: 30302051 PMCID: PMC6175749 DOI: 10.1016/j.jceh.2018.04.015
Source DB: PubMed Journal: J Clin Exp Hepatol ISSN: 0973-6883