Iacoban Cosmin, Lebioda Konrad, Patel Kartik, León Ada Baisre-de, Lee Huey-Jen
Department of Radiology, New Jersey Medical School, Rutgers University, 150 Bergen Street, Newark, New Jersey.
Department of Pathology, Immunology and Laboratory Medicine, New Jersey Medical School, Rutgers University, 185 South Orange Avenue, Newark, New Jersey.
Radiol Case Rep. 2021 Dec 20;17(3):599-603. doi: 10.1016/j.radcr.2021.11.015. eCollection 2022 Mar.
Epithelioid type leiomyosarcoma is rarely encountered outside of the abdomen or uterus. We present a case of posterior mediastinal leiomyosarcoma in a 45-year-old male with back pain and bilateral lower extremity weakness. Magnetic Resonance Imaging of the thoracic spine revealed a heterogeneous posterior mediastinal soft tissue mass infiltrating the vertebral body and epidural space with resultant spinal cord compression and edema. Positron Emission Tomography showed no evidence of distant metastatic spread. Histopathological characterization revealed epithelial type leiomyosarcoma. Despite multiple subtotal resections, radiotherapy, and salvage chemotherapy with successful restoration of the patient's neurological function, the tumor burden remained significant. The patient was subsequently lost to follow up and the clinical outcome remains unknown. To our knowledge this is the first reported case of epithelioid type posterior mediastinal leiomyosarcoma presenting with spinal cord compression and edema.
上皮样型平滑肌肉瘤在腹部或子宫以外很少见。我们报告一例45岁男性后纵隔平滑肌肉瘤,患者有背痛和双侧下肢无力症状。胸椎磁共振成像显示后纵隔有一个不均匀的软组织肿块,浸润椎体和硬膜外间隙,导致脊髓受压和水肿。正电子发射断层扫描显示无远处转移扩散迹象。组织病理学特征显示为上皮样型平滑肌肉瘤。尽管进行了多次次全切除、放疗和挽救性化疗,患者神经功能成功恢复,但肿瘤负荷仍然很大。该患者随后失访,临床结局未知。据我们所知,这是首例报告的上皮样型后纵隔平滑肌肉瘤伴脊髓受压和水肿的病例。