Iatrogenic cerebral amyloid angiopathy: Two cases linked to childhood cadaveric dural transplantation for different intracranial pathologies, diagnosed using the simplified Edinburgh computed tomography criteria.

Surgical neurology international Pub Date : 2025-05-02 eCollection Date: 2025-01-01 DOI:10.25259/SNI_245_2025
Senta Frol, Matija Zupan, Janja Pretnar Oblak, Tomaž Velnar, Bruno Splavski
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Abstract

Background: Cerebral amyloid angiopathy (CAA) is an age-related condition marked by amyloid-β (Aβ) accumulation in the small cerebral vessels. Iatrogenic cerebral amyloid angiopathy (iCAA) is a distinct form of CAA in younger patients with a history of cranial surgeries involving cadaveric dural transplants. Both iCAA and CAA are linked to recurrent lobar intracerebral hemorrhage (ICH). This article highlights iCAA as a distinct variant, discussing the possibility of using simplified Edinburgh computed tomography (CT) criteria as a possible diagnostic tool for CAA and carefully considering plausible childhood surgery, with the risk of Aβ transmission through dural grafts in all, especially middle-aged patients.

Case description: We present two cases of iCAA in a 46-year-old female and a 52-year-old male who suffered recurrent spontaneous lobar ICHs. The CAA was diagnosed using the simplified Edinburgh CT criteria, leading to further investigations into the underlying pathology. Based on their age, iCAA was suspected, and only after a meticulous search of the hospital documentation it was discovered that they both underwent cranial surgeries in childhood involving cadaveric dural grafts. The diagnosis of iCAA was established using the proposed diagnostic criteria by Banerjee et al. and later confirmed by pathological examination.

Conclusion: Our paper emphasizes the simplified Edinburgh criteria as a potential yet preliminary diagnostic tool for iCAA, while also highlighting the long-term risks of iatrogenic amyloid transmission related to dural grafting following various neurosurgical procedures.

医源性脑淀粉样血管病:两例与儿童尸体硬脑膜移植有关的不同颅内病理,使用简化的爱丁堡计算机断层扫描标准诊断。
背景:脑淀粉样血管病(CAA)是一种以小脑血管中淀粉样蛋白-β (Aβ)积累为特征的与年龄相关的疾病。医源性脑淀粉样血管病(iCAA)是一种不同形式的CAA,发生于有颅脑手术史的年轻患者,涉及尸体硬脑膜移植。iCAA和CAA都与复发性大叶性脑出血(ICH)有关。本文强调iCAA是一种不同的变体,讨论了使用简化的爱丁堡计算机断层扫描(CT)标准作为CAA可能的诊断工具的可能性,并仔细考虑可行的儿童手术,所有患者,特别是中年患者,都有通过硬脑膜移植物传播a β的风险。病例描述:我们报告两例iCAA患者,一名46岁的女性和一名52岁的男性,他们遭受了复发的自发性大叶性ICHs。使用简化的爱丁堡CT标准诊断CAA,从而进一步研究潜在病理。根据他们的年龄,怀疑他们是iCAA,在仔细查阅医院文件后才发现,他们都在童年时期接受了涉及尸体硬脑膜移植的颅脑手术。根据Banerjee等人提出的诊断标准建立iCAA的诊断,并经病理检查证实。结论:我们的论文强调了简化的爱丁堡标准作为iCAA潜在的初步诊断工具,同时也强调了各种神经外科手术后与硬脑膜移植相关的医源性淀粉样蛋白传递的长期风险。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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