Pishdad Parisa, Soltani Amirhossein, Houshi Shakiba, Salimi Mohsen
Department of Radiology, Shiraz University of Medical Sciences, Shiraz, Iran.
Medical Imaging Research Center, Shiraz University of Medical Sciences, Shiraz, Iran.
Radiol Case Rep. 2025 Jan 17;20(4):1871-1876. doi: 10.1016/j.radcr.2025.01.011. eCollection 2025 Apr.
This report describes the case of a 35-year-old woman with a recurrent ruptured intracranial dermoid cyst. These rare congenital lesions account for less than 1% of intracranial tumors globally. The patient was first diagnosed in her adolescence and underwent surgical excision with shunt placement at the age of 23, which provided symptom relief for 6 years. Her symptoms later recurred, including headaches, blurred vision, and progressive weakness. Imaging revealed a hemorrhagic lobulated mass that compressed the brainstem, encased vascular structures, caused a midline shift, and led to ventricular dilation. These findings suggested possible incomplete removal of the cyst wall during the initial surgery. This case highlights the challenges of diagnosing and managing recurrent intracranial dermoid cysts. It emphasizes the need for long-term monitoring, detailed imaging to assess recurrence and complications, and a multidisciplinary approach to treatment to improve outcomes.
本报告描述了一名35岁复发性颅内皮样囊肿破裂女性的病例。这些罕见的先天性病变在全球颅内肿瘤中占比不到1%。该患者在青春期首次被诊断出,并于23岁时接受了手术切除并放置分流管,症状缓解了6年。她的症状后来复发,包括头痛、视力模糊和进行性虚弱。影像学检查显示一个出血性分叶状肿块,压迫脑干,包裹血管结构,导致中线移位并引起脑室扩张。这些发现提示初次手术时可能未完全切除囊肿壁。该病例突出了复发性颅内皮样囊肿诊断和管理的挑战。它强调了长期监测、详细影像学检查以评估复发和并发症的必要性,以及采用多学科治疗方法以改善治疗效果的重要性。