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当动脉瘤伪装成肿瘤时:小儿患者中血栓形成的小脑后下动脉动脉瘤酷似肿瘤。病例说明

When an aneurysm pretends to be a tumor: thrombosed posterior inferior cerebellar artery aneurysm mimicking a neoplasm in a pediatric patient. Illustrative case.

作者信息

Neyazi Belal, Swiatek Vanessa Magdalena, Schwab Roland, Mawrin Christian, Stein Klaus-Peter, Rashidi Ali, Behme Daniel, Sandalcioglu I Erol

机构信息

Department of Neurosurgery, Otto-von-Guericke University, Magdeburg, Saxony-Anhalt, Germany.

Department of Neuroradiology, Otto-von-Guericke University, Magdeburg, Saxony-Anhalt, Germany.

出版信息

J Neurosurg Case Lessons. 2025 Jun 16;9(24). doi: 10.3171/CASE2592.

Abstract

BACKGROUND

Thrombosed intracranial aneurysms are rare in pediatric populations and pose significant diagnostic challenges due to their atypical imaging features, which often mimic neoplasms. These lesions can present with mass effect, contrast enhancement, and calcifications, leading to potential misdiagnosis and inappropriate management. Accurate differentiation through advanced imaging is essential to prevent surgical complications and ensure optimal outcomes.

OBSERVATIONS

The authors describe the case of a 15-year-old boy with severe acute headaches and an MRI finding of a contrast-enhancing lesion in the left cerebellar tonsil abutting the medulla oblongata, suggestive of a neoplasm. Neurological examination was normal, and there was no significant medical history. Despite negative angiographic findings, the unclear etiology warranted surgical intervention. A median suboccipital craniotomy revealed a capsule-like lesion with arterial feeders from the posterior inferior cerebellar artery. Complete resection was achieved, and histopathology confirmed a thrombosed aneurysm. Postoperative recovery was uneventful, and 1-year follow-up showed full symptom resolution without recurrence.

LESSONS

This case highlights the importance of considering thrombosed aneurysms in pediatric patients with atypical intracranial lesions. Multidisciplinary collaboration and advanced imaging are crucial for accurate diagnosis and effective management. Documenting such cases enhances understanding, refines diagnostic strategies, and improves patient care. https://thejns.org/doi/10.3171/CASE2592.

摘要

背景

血栓形成的颅内动脉瘤在儿科人群中较为罕见,因其不典型的影像学特征常类似肿瘤,故带来重大的诊断挑战。这些病变可表现为占位效应、强化及钙化,导致可能的误诊及不恰当的处理。通过先进影像学进行准确鉴别对于预防手术并发症及确保最佳治疗效果至关重要。

观察

作者描述了一名15岁男孩的病例,该男孩有严重急性头痛,磁共振成像(MRI)发现左小脑扁桃体有一强化病变,紧邻延髓,提示肿瘤。神经系统检查正常,且无重要病史。尽管血管造影结果为阴性,但病因不明仍需手术干预。枕下正中开颅术显示一个囊样病变,有来自小脑后下动脉的供血支。实现了完整切除,组织病理学证实为血栓形成的动脉瘤。术后恢复顺利,1年随访显示症状完全缓解且无复发。

经验教训

该病例凸显了在患有非典型颅内病变的儿科患者中考虑血栓形成的动脉瘤的重要性。多学科协作及先进影像学对于准确诊断及有效治疗至关重要。记录此类病例可增进理解、完善诊断策略并改善患者护理。https://thejns.org/doi/10.3171/CASE2592

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2ff1/12171099/8ddad9534164/CASE2592_figure_1.jpg

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