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成年女性鞍上表皮样囊肿,表现为失忆和嗜睡:一例罕见病例报告

Suprasellar epidermoid cyst in an adult female, presenting as amnesia and somnolence: A rare case report.

作者信息

Esmat Habib Ahmad

机构信息

Department of Radiology, Kabul University of Medical Sciences, Kabul, Afghanistan; Fellow of Radiology at EGE University Hospital, Izmir, Turkey.

出版信息

Int J Surg Case Rep. 2020;77:565-569. doi: 10.1016/j.ijscr.2020.11.093. Epub 2020 Nov 20.

Abstract

INTRODUCTION

Intracranial epidermoid cysts (ECs) are rare benign congenital lesions and account for approximately 0.3 to 1.8% of all intracranial brain tumors. They frequently occur at the cerebellopontine angles and parasellar regions, insinuating between brain structures. The author reports here a case of pathologically proven suprasellar epidermoid cyst in an adult female, presented with amnesia and somnolence to increase awareness about this unusual presentation.

CASE REPORT

A 58-year-old female was presented to our hospital complaining of amnesia for one year, followed by weakness and somnolence for 2 months. Radiological imaging showed the features of the suprasellar epidermoid cyst which resected through the transsphenoidal endoscopic approach.

DISCUSSION

Epidermoid cysts are slow-growing, benign lesions however, they may rarely undergo malignant transformation into a squamous cell carcinoma. The mean age at presentation of these lesions is 40 years. Suprasellar/sellar lesions usually present with non-specific headaches and visual disturbances. However, our case presented with amnesia and somnolence.

CONCLUSION

Surasellare epidermoid cysts (ECs) are rare benign congenital lesions. They often manifest with headache and visual field defects but, they may present with atypical symptoms as amnesia and somnolence. Endoscopic transnasal and trans-sphenoidal approaches can help to remove the lesion in most cases. Attention needs to the possible postoperative complications and longtime imaging follow-up because this lesion may recur after a few years.

摘要

引言

颅内表皮样囊肿(ECs)是罕见的良性先天性病变,约占所有颅内脑肿瘤的0.3%至1.8%。它们常发生于桥小脑角和鞍旁区域,在脑结构之间蔓延。作者在此报告一例经病理证实的成年女性鞍上表皮样囊肿病例,该病例表现为失忆和嗜睡,以提高对这种不寻常表现的认识。

病例报告

一名58岁女性因失忆一年、继以乏力和嗜睡2个月前来我院就诊。影像学检查显示为鞍上表皮样囊肿的特征,通过经蝶窦内镜手术切除。

讨论

表皮样囊肿是生长缓慢的良性病变,然而,它们很少会恶变成为鳞状细胞癌。这些病变的平均发病年龄为40岁。鞍上/鞍区病变通常表现为非特异性头痛和视觉障碍。然而,我们的病例表现为失忆和嗜睡。

结论

鞍上表皮样囊肿(ECs)是罕见的良性先天性病变。它们常表现为头痛和视野缺损,但也可能出现失忆和嗜睡等非典型症状。在大多数情况下,内镜经鼻和经蝶窦入路有助于切除病变。需要注意可能的术后并发症以及长期的影像学随访,因为这种病变可能在数年后复发。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3e8d/7701884/2e528fb15a3c/gr1.jpg

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