Leiomyosarcoma of the Mediastinum Depicted on CT Images: A Rare Origin Case and Literature Review

Authors

  • Yuanyuan Wang Department of Radiology, West China Hospital of Sichuan University, China
  • Zhaochu Chen Internal Medicine Dept. 4, Sichuan Provincial General Hospital of Judicial Police, China
  • Jianqun Yu Department of Radiology, West China Hospital of Sichuan University, China

DOI:

https://doi.org/10.3941/jrcr.5800

Abstract

Introduction: Leiomyosarcoma (LMS), a malignant smooth muscle tumor, accounts for 10%–20% of soft tissue sarcomas. Primary mediastinal LMS is rare, with only 13 cases reported in the last two decades. This study aims to delineate its clinical and radiological characteristics through a novel case presentation and literature review. Methods: We report the case of a 57-year-old male presenting with progressive dyspnea and back pain. Diagnostic workup included contrastenhanced chest CT, histopathological analysis of CT-guided biopsy specimens, and immunohistochemical staining (positive for Vim, Des, SMA, and Calponin; negative for S100 and CD34). A systematic PubMed review of mediastinal LMS cases was performed to summarize imaging and pathological features.

Results: Imaging revealed a 16.1 × 10.9 cm heterogeneous posterior mediastinal mass with necrotic foci, vascular encasement, and right pleural effusion. Histopathology showed spindle-shaped tumor cells with a Ki-67 index of 40%, confirming LMS. Literature synthesis (n=14 cases) demonstrated that 71.4% of tumors exceeded 5 cm, with a predilection for the anterior mediastinum (71.4%) and heterogeneous enhancement (100%).

Discussion: Mediastinal LMS radiologically mimics other malignancies but exhibits distinctive pathological markers (SMA/ Desmin+). Surgical resection remains the primary treatment; our patient received neoadjuvant chemotherapy (liposomal doxorubicin/dacarbazine) and achieved a partial response. This case highlights the importance of multidisciplinary collaboration (imaging-pathology correlation) for the timely diagnosis of this aggressive neoplasm.

A: Non-contrast chest CT demonstrates a soft tissue mass located in the posterior mediastinum (white arrow indicates); B-C (Enhanced arterial and venous phases): The contrast-enhanced CT reveals a posterior mediastinal mass compressing the adjacent left atrium and pulmonary venous trunk (white arrow indicates); D: Non-contrast chest CT demonstrates a soft tissue mass located in the posterior mediastinum (white arrow indicates); E–H (Figures E, G and H show the arterial phase, while Figure F shows the venous phase): Contrast-enhanced chest CT (axial, coronal, and sagittal views) reveals a heterogeneously enhancing soft tissue mass in the posterior mediastinum (white arrow indicates), adjacent structures are compressed, and necrotic areas are observed within the lesion. Multiple small intralesional vascular structures are observed (red arrow indicates). The esophagus appears compressed and narrowed, and the interface between the lesion and the descending aorta is indistinct. I: Narrowing of a segmental bronchus in the right lung, accompanied by compression-induced consolidation and partial atelectasis.

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Published

2025-07-31

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Section

Thoracic Radiology