Leiomyosarcoma (LMS) is a rare and aggressive soft tissue tumor with various clinical characteristics and treatment challenges. Inflammatory leiomyosarcoma (ILMS) has been identified as a distinct entity, characterized by a primitive myogenic phenotype and frequent co-expression of smooth and skeletal muscle markers. A study reported on nine cases of ILMS, highlighting its indolent clinical course despite a lack of long-term follow-up data. Genetic profiling of ILMS revealed a near haploid genome and upregulation of genes crucial for skeletal muscle differentiation, suggesting a unique biological behavior that may influence treatment strategies (ref: Michal doi.org/10.1007/s00428-020-02774-z/). Additionally, primary iliocaval leiomyosarcomas (ICLM) present significant treatment challenges, as they are aggressive and typically require surgical intervention. A study focused on chemotherapy-naïve ICLM patients emphasized the need for further research to improve oncological outcomes, particularly regarding the role of chemoradiotherapy in the neo/adjuvant setting (ref: Ong doi.org/10.1016/j.ejso.2020.01.034/). Furthermore, a population-based analysis of adult genitourinary sarcomas revealed that leiomyosarcomas originating in the bladder had the longest median survival time of 62 months, contrasting sharply with carcinosarcomas, which had a median survival of only 9 months. This study underscores the variability in outcomes based on tumor location and histological subtype (ref: Nazemi doi.org/10.1016/j.urolonc.2019.12.004/).