Alkhaledi Ahmad, Hanafi Ibrahem, Alsabe Hassan, Chatty Eyad M
Faculty of Medicine, Damascus University, Damascus, Syria.
Division of Neurology, Department of Internal Medicine, Faculty of Medicine, Damascus University, Damascus, Syria.
Oxf Med Case Reports. 2019 Mar 29;2019(3):omz017. doi: 10.1093/omcr/omz017. eCollection 2019 Mar.
Rhabdomyosarcoma (RMS) is a malignant soft tissue tumor, usually presenting in the head and neck in children, with frequent metastases to the lungs. In this report, we present a rare case of a post-menopausal RMS patient who presented with walking difficulties after hysterectomy. A computerized tomography scan revealed metastases spreading to the mediastinum, retroperitoneum, lungs, liver and bones. On a protocol of Gemcitabine and Carboplatin, the patient showed stability in the dimensions of the masses with significant improvement in her quality of life.
横纹肌肉瘤（RMS）是一种恶性软组织肿瘤，通常发生于儿童的头颈部，常转移至肺部。在本报告中，我们呈现了一例罕见的绝经后RMS患者，该患者在子宫切除术后出现行走困难。计算机断层扫描显示转移灶扩散至纵隔、腹膜后、肺、肝和骨骼。在接受吉西他滨和卡铂治疗方案后，患者肿块大小保持稳定，生活质量有显著改善。
