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原发性双侧枕叶包虫囊肿:一例罕见病例报告

Primary bilateral occipital hydatid cysts: Report of a rare entity.

作者信息

Hermassi Mohamed Aziz, Guediche Skander, Zouaghi Mohamed, Bedioui Aziz, Hamza Meissa, Bahri Kamel

机构信息

Department of Neurosurgery, Traumatology and Severe Burns Center, Ben Arous, Tunisia.

出版信息

Int J Surg Case Rep. 2024 Nov;124:110464. doi: 10.1016/j.ijscr.2024.110464. Epub 2024 Oct 16.

Abstract

INTRODUCTION AND IMPORTANCE

Hydatidosis is a cosmopolitan zoonosis caused by larval stages of Echinococcus granulosus. The brain is a rare location for this disease to occur, especially in adults. The occipital location is extremely unusual and the cysts are usually solitary. Cerebral hydatid cysts may be primary or secondary. Primary multiple bilateral cerebral hydatid cysts are extremely uncommon. This case aims to highlight the diagnostic process and surgical management of primary bilateral hydatid cysts.

CASE PRESENTATION

We present the case of a 36-year-old Tunisian man admitted to our institution for headache and visual impairments. Neurological examination revealed bilateral decreased visual acuity. Cranial MRI showed two primary bilateral occipital hydatid cysts. The patient underwent successful surgical excision using two craniotomies in a single procedure.

CLINICAL DISCUSSION

Primary multiple bilateral cerebral hydatid cysts are extremely rare. The pathogenetic mechanisms of this entity are not yet precisely known. Clinical symptoms vary depending on the location of the cysts in the brain. Several diagnostic methods can be used, computed tomography and especially magnetic resonance imaging, which represent the gold standard in the diagnosis of multiple and bilateral cerebral hydatid cysts. The treatment of primary multiple hydatid cysts is exclusively surgical. The key to an optimal result is careful surgical technique that avoids preoperative ruptures and complications.

CONCLUSION

Primary multiple cerebral hydatidosis is extremely rare, even in endemic areas. Diagnosis is by imaging techniques and treatment is primarily surgical. With a careful surgical strategy and appropriate postoperative management, patients can recover without neurological sequelae.

摘要

引言与重要性

包虫病是一种由细粒棘球绦虫幼虫阶段引起的全球性人畜共患病。脑部是该疾病罕见的发病部位,尤其是在成年人中。枕部发病极为罕见,且囊肿通常为单发。脑包虫囊肿可为原发性或继发性。原发性双侧多发性脑包虫囊肿极为罕见。本病例旨在强调原发性双侧脑包虫囊肿的诊断过程及手术治疗。

病例介绍

我们报告一例36岁突尼斯男性患者,因头痛和视力障碍入住我院。神经系统检查显示双侧视力下降。头颅磁共振成像(MRI)显示双侧枕部有两个原发性脑包虫囊肿。患者在一次手术中通过两次开颅手术成功切除囊肿。

临床讨论

原发性双侧多发性脑包虫囊肿极为罕见。该疾病的确切发病机制尚不清楚。临床症状因囊肿在脑内的位置而异。可采用多种诊断方法,计算机断层扫描(CT)尤其是磁共振成像(MRI),后者是诊断双侧多发性脑包虫囊肿的金标准。原发性多发性包虫囊肿的治疗只能通过手术进行。取得最佳治疗效果的关键在于仔细的手术操作技术,避免术前囊肿破裂及并发症。

结论

原发性多发性脑包虫病极为罕见,即使在流行地区也是如此。诊断依靠影像学技术,治疗主要是手术。通过仔细的手术策略和适当的术后管理,患者可无神经后遗症地康复。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d90/11513667/624c5ea74c26/gr1.jpg

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