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一例罕见脑包虫囊肿的病例报告。

A case report of an unusual cerebral hydatid cyst.

作者信息

Ahmed Mubasher, Basurrah Abdulaziz A, Brinji Zaina Siraj, Albargi Naseem, El-Fattah Mona Abd, Alnashiwaaty Omar, Aljohani Mona Shadad, Alkhotani Alaa, Farag Ahmed Adel

机构信息

Department of Neurosurgery, King Abdullah Medical City, Makkah, Saudi Arabia.

Department of Radiology, King Abdullah Medical City, Makkah, Saudi Arabia.

出版信息

Surg Neurol Int. 2024 Mar 22;15:99. doi: 10.25259/SNI_70_2024. eCollection 2024.

Abstract

BACKGROUND

Intracranial hydatid cyst is an exceedingly uncommon condition. Typically, it manifests as hydatid cysts in the liver, lungs, kidney, and spleen. In this report, we present a rare case of a hydatid cyst located in the brain, exhibiting atypical radiological characteristics, and successfully treated with complete microsurgical excision.

CASE DESCRIPTION

A 45-year-old male, a former smoker, presented with a new-onset seizure. Brain imaging revealed a solitary, intra-axial, and cystic lesion with wall enhancement in the right temporal region. The cyst extended into the temporal horn of the right lateral ventricle, surrounded by mild edema. Differential diagnoses included brain metastasis, abscess, and tuberculoma. However, following computed tomography (CT) scans of the chest, abdomen, and pelvis (CAP) and serological tests, the provisional diagnosis included a hydatid cyst. The CT CAP showed diffuse non-specific cystic lesions of variable sizes in the liver and spleen, along with numerous bilateral pulmonary cysts. A right temporal craniotomy was performed, and the cyst was microsurgically excised without rupture. Microscopic and histopathological examination confirmed the presence of a hydatid cyst.

CONCLUSION

Intracranial hydatid cyst is an extremely rare condition and should always be considered a possible differential diagnosis in cases of cerebral cystic lesions. Hydrodissection is the preferred surgical method for resection; however, in atypical cases such as the one described here, meticulous dissection of the cyst capsule from the brain parenchyma may be successful with minimal risk of intraoperative rupture.

摘要

背景

颅内包虫囊肿是一种极为罕见的病症。通常情况下,包虫囊肿多表现于肝脏、肺、肾脏和脾脏。在本报告中,我们呈现了一例罕见的位于脑部的包虫囊肿病例,该病例具有非典型的放射学特征,并通过完整的显微手术切除成功治愈。

病例描述

一名45岁男性,既往有吸烟史,因新发癫痫就诊。脑部影像学检查显示右侧颞叶有一个孤立的、轴内囊性病变,伴有壁强化。囊肿延伸至右侧侧脑室颞角,周围有轻度水肿。鉴别诊断包括脑转移瘤、脓肿和结核瘤。然而,经胸部、腹部和骨盆(CAP)计算机断层扫描(CT)及血清学检查后,初步诊断为包虫囊肿。CT CAP显示肝脏和脾脏有大小不一的弥漫性非特异性囊性病变,以及双侧多发肺囊肿。行右侧颞叶开颅手术,通过显微手术完整切除囊肿且未破裂。显微镜检查和组织病理学检查证实为包虫囊肿。

结论

颅内包虫囊肿极为罕见,在脑囊性病变病例中应始终将其视为可能的鉴别诊断。水分离是首选的手术切除方法;然而,在此类非典型病例中,如本报告所述,从脑实质细致剥离囊肿包膜可能成功,且术中破裂风险最小。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d326/11021106/e41cac1972d5/SNI-15-99-g001.jpg

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