Frol Senta, Zupan Matija, Pretnar Oblak Janja, Velnar Tomaž, Splavski Bruno
Department of Vascular Neurology, University Medical Center Ljubljana, Ljubljana, Slovenia.
Department of Neurosurgery, University Medical Center Ljubljana, Ljubljana, Slovenia.
Surg Neurol Int. 2025 May 2;16:165. doi: 10.25259/SNI_245_2025. eCollection 2025.
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.
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 . and later confirmed by pathological examination.
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.
脑淀粉样血管病(CAA)是一种与年龄相关的疾病,其特征是淀粉样β蛋白(Aβ)在脑小血管中积聚。医源性脑淀粉样血管病(iCAA)是CAA的一种特殊形式,见于有涉及尸体硬脑膜移植的颅脑手术史的年轻患者。iCAA和CAA均与复发性脑叶脑出血(ICH)有关。本文重点介绍iCAA这一特殊变体,讨论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,并认真考虑可能的儿童期手术,尤其是所有患者,尤其是中年患者中存在通过硬脑膜移植物传播Aβ的风险。
我们报告了两例iCAA病例,分别为一名46岁女性和一名52岁男性,他们均患有复发性自发性脑叶ICH。使用简化的爱丁堡CT标准诊断为CAA,从而对潜在病理进行了进一步调查。基于他们的年龄,怀疑为iCAA,只有在仔细查阅医院病历后才发现他们两人在儿童期都接受过涉及尸体硬脑膜移植的颅脑手术。使用Banerjee提出的诊断标准确诊为iCAA, 随后经病理检查证实。
我们的论文强调简化的爱丁堡标准作为iCAA一种潜在但初步的诊断工具,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播的长期风险。