小脑内许旺瘤的罕见表现:病例报告。

IF 0.7 Q4 PATHOLOGY
Case Reports in Pathology Pub Date : 2024-10-16 eCollection Date: 2024-01-01 DOI:10.1155/2024/8678186
Mohamed Alhantoobi, Nadeen Alkhoori, Hassan Khayat, Euan Zhang, Almunder Algird, John Provias
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引用次数: 0

摘要

背景:小脑内分裂瘤是一种极为罕见的疾病,文献中仅有 21 例报道。病例描述一名 68 岁的男性因长期头痛、头晕、步态失衡和不协调而就诊。先前的磁共振成像显示右侧小脑有囊性病变,但患者已失去随访机会。最新的磁共振成像显示病灶急剧增大,而且临床状况不断恶化。患者成功接受了手术切除。结论小脑内分裂瘤由于罕见,术前诊断具有挑战性;但是,应将其纳入小脑囊性病变的鉴别诊断中,大多数病例可通过完全手术切除获得成功治疗。病理检查显示这是一种纺锤形细胞肿瘤,具有其他典型的裂隙细胞瘤组织病理学特征。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A Rare Presentation of Intracerebellar Schwannoma: A Case Report.

Background: Intracerebellar schwannoma is an extremely rare disease entity with only 21 case reports described in the literature. Case Description: A 68-year-old male presented with chronic headaches, dizziness, gait imbalance, and incoordination. Previous MRI had revealed a cystic lesion in the right cerebellum; however, patient was lost to follow-up. Updated MRI revealed dramatic enlargement of the lesion in addition to worsening clinical status. The patient underwent successful surgical resection. Conclusion: Intracerebellar schwannoma can be challenging to diagnose preoperatively due to its rare occurrence; however, it should be included in the differential diagnosis of cystic lesions in the cerebellum, and most cases can be successfully treated with complete surgical resection. Pathological examination revealed a spindle cell neoplasm with other typical histopathological features of schwannoma.

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