小脑上皮样囊肿:病例报告

Chengye Hou, Yuanqin Liu, Feng Li, Qinglu Zhang
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摘要

理由 颅内附睾囊肿相对罕见。本病例报告的重点是一名被诊断出患有附脑囊肿并接受了手术治疗的患者。术后病理检查证实该病变位于小脑。主诉 一位 32 岁的女性患者以头晕和头痛为主诉,过去 1 年中没有任何诱发因素。她还报告说,在过去两周内,症状的频率和强度都有所增加。诊断 颅脑磁共振成像(MRI)显示,小脑苍白球下的脑干左后部有一圆形长T1和T2异常信号灶。病灶边界清晰,大小约为 4.0 × 3.1 × 3.2 厘米,未显示任何明确的强化。在完成术前检查后,对病灶进行了全切除。治疗结果。患者在术后第 11 天症状消失后出院。四肢的感觉和运动功能未受治疗影响。经验 小脑上皮样囊肿很少见,大多数患者仅因脑水肿而感到不适。仅通过影像学检查也很难将这些病变与其他颅内囊肿区分开来。本研究旨在报告一例罕见的小脑上皮样囊肿病例,以便为今后的诊断和治疗提供参考。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Cerebellar ependymal cyst: a case report
Rationale Intracranial ependymal cysts are relatively rare. The current case report focuses on a patient who was diagnosed with an ependymal cyst and underwent surgical treatment. Postoperative pathological examination confirmed the presence of this lesion in the cerebellum. Chief complaint A 32-year-old female patient presented with a chief complaint of dizziness and headache with no triggers for the past 1 year. She also reported an increase in the frequency and intensity of symptoms in the past 2 weeks. Diagnosis Cranial magnetic resonance imaging (MRI) showed a rounded long T1 and T2 abnormal signal foci in the left posterior part of the brainstem under the cerebellar pallidum. The lesion had a clear boundary, was approximately 4.0 × 3.1 × 3.2 cm in size, and did not exhibit any definitive enhancement. Interventions Total resection of the lesion was carried out after completion of the preoperative examination. Treatment outcomes. The patient was discharged from the hospital on postoperative day 11 once their symptoms had disappeared. The sensory and motor functions of the limbs remained unaffected by treatment. Experiences Cerebellum ependymal cysts are rare, and most patients only experience discomfort due to cerebral edema. These lesions are also often difficult to differentiate from other intracranial cysts using imaging alone. The aim of this study was to report a rare case of ependymal cyst so that it may serve as a reference for diagnosis and treatment in the future.
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