皮样瘤伴胫外凸

Krishna Prabhu MCh , Roy Thomas Daniel MCh , Sunithi Mani MD , Ari G. Chacko MCh
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引用次数: 7

摘要

皮样瘤是一种罕见的先天性病变,约占颅内肿瘤的0.2% ~ 1.8%。皮样瘤合并胫外凸是非常罕见的。病例描述:我们报告一位成年女性的皮样瘤,其位置和形态都不寻常。病变有2个主要组成部分,在囊肿内有不同的物质。皮样的后部出现在第四脑室的底部,将脑桥分成两半。病变前部位于脑干前池,环绕脑干前半部分。病变被彻底切除,术后图像显示桥的两半在中线重合。结论:本病例报告显示了这一极其不寻常的皮样囊肿伴髋外侧畸形的解剖特点。通过背侧入路完全切除病变获得了良好的结果。
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Dermoid tumor with diastematobulbia

Background

Dermoid tumors are rare congenital lesions and account for 0.2% to 1.8% of all intracranial tumors. Dermoid tumor with diastematobulbia is very rare.

Case description

We report a dermoid tumor in an adult female with an unusual location and morphology. The lesion had 2 major components with different material within the cysts. The posterior part of the dermoid had presented on the floor of the fourth ventricle and had split the pons into 2 distinct halves. The anterior part of the lesion was situated in the prepontine cistern and encircling the anterior half of the brainstem. The lesion was radically excised, and the postoperative images showed return of the 2 halves of the pons to appose each other in the midline.

Conclusion

This case report demonstrates the anatomical peculiarities of this extremely unusual presentation of a dermoid cyst with diastematobulbia. Total excision of the lesion through a dorsal approach resulted in a good outcome.

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来源期刊
Surgical Neurology
Surgical Neurology 医学-临床神经学
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