Clinical and radiological presentation of cavernomas according to the Zabramski classification.

IF 3.6 2区 医学 Q1 CLINICAL NEUROLOGY Journal of neurosurgery Pub Date : 2025-01-31 Print Date: 2025-06-01 DOI:10.3171/2024.8.JNS24246
Emilia Saari, Timo Koivisto, Tuomas Rauramaa, Juhana Frösen
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Abstract

Objective: Cerebral cavernous malformations (CCMs) are a cluster of abnormal vessels of the brain. CCMs have a low risk for intracerebral hemorrhage and appear increasingly often as incidental findings on MRI. Zabramski classification has been used to describe the radiological features of CCMs. How the Zabramski classification associates with the clinical symptoms at presentation and clinical course of the disease is not well established.

Methods: The authors reviewed the medical records of conservatively managed and surgically treated CCM patients over a 20-year period treated in Kuopio and Tampere University Hospitals. Both clinical and radiological data were analyzed. The modified Rankin Scale (mRS) was used to score the symptoms.

Results: Altogether, 775 CCM patients were identified. In both cohorts, most patients were asymptomatic (53% in the Kuopio University Hospital [KUH] cohort and 64% in the Tampere University Hospital [TAUH] cohort). Most CCMs were located supratentorially (77%, 661/858), and most patients presented with epileptic seizures. Of the infratentorial CCMs, most were located in the cerebellum (61%, 121/198). The most common symptoms caused by these CCMs were double vision, sensory deficits, and impaired balance. The median mRS score for symptoms in all CCMs was 0, and if only symptomatic CCMs were accounted for, it was 2. Most CCMs were Zabramski type II, and these CCMs were relatively asymptomatic, similar to Zabramski type III CCMs. Zabramski type I CCMs were mostly symptomatic, whereas Zabramski type IV CCMs were completely asymptomatic. Of patients with type I CCMs, approximately 15% developed new symptoms within 1 year, and in the long-term follow-up 26% had new symptoms. In radiological follow-up, 81% of the type I CCMs regressed to type II or III. Of type II or III CCMs, 2.3% changed over time to type I. Age was associated with the Zabramski classification (p < 0.001 in the TAUH cohort and p = 0.034 in the KUH cohort).

Conclusions: Most CCMs are asymptomatic, incidental findings, in particular, nearly all Zabramski type IV CCMs. If symptoms are present, they are mainly associated with Zabramski type I CCMs and occasionally with Zabramski type II or III CCMs. Although most Zabramski type I CCMs will regress to type II or III and remain asymptomatic, over long-term follow-up, up to one-quarter develop new symptoms.

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根据Zabramski分类的海绵状瘤的临床和影像学表现。
目的:脑海绵状血管瘤是一组异常的脑血管。CCMs发生脑出血的风险较低,并且越来越多地在MRI上作为偶然发现出现。Zabramski分类已被用于描述ccm的放射学特征。Zabramski分类如何与临床症状和疾病的临床病程相关联尚不清楚。方法:作者回顾了库奥皮奥和坦佩雷大学医院20年来保守管理和手术治疗的CCM患者的医疗记录。对临床和放射学资料进行分析。采用改良Rankin量表(mRS)对症状进行评分。结果:共发现775例CCM患者。在这两个队列中,大多数患者无症状(库奥皮奥大学医院[KUH]队列中为53%,坦佩雷大学医院[TAUH]队列中为64%)。大多数ccm位于幕上(77%,661/858),大多数患者表现为癫痫发作。在幕下CCMs中,大多数位于小脑(61%,121/198)。这些CCMs引起的最常见症状是重视、感觉缺陷和平衡受损。所有ccm症状的mRS评分中位数为0,如果只考虑症状性ccm,则为2。大多数CCMs为Zabramski II型,这些CCMs相对无症状,与Zabramski III型CCMs相似。Zabramski型CCMs以症状为主,而Zabramski型CCMs则完全无症状。在I型CCMs患者中,约15%的患者在1年内出现新症状,26%的患者在长期随访中出现新症状。在放射学随访中,81%的I型CCMs退化为II或III型。在II型或III型CCMs中,2.3%随着时间的推移转变为i型。年龄与Zabramski分类相关(TAUH组p < 0.001, KUH组p = 0.034)。结论:大多数ccm是无症状的,偶然发现,特别是几乎所有的Zabramski IV型ccm。如果出现症状,它们主要与Zabramski I型CCMs有关,偶尔与Zabramski II型或III型CCMs有关。虽然大多数Zabramski I型CCMs会退化为II型或III型并保持无症状,但经过长期随访,高达四分之一的CCMs会出现新症状。
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来源期刊
Journal of neurosurgery
Journal of neurosurgery 医学-临床神经学
CiteScore
7.20
自引率
7.30%
发文量
1003
审稿时长
1 months
期刊介绍: The Journal of Neurosurgery, Journal of Neurosurgery: Spine, Journal of Neurosurgery: Pediatrics, and Neurosurgical Focus are devoted to the publication of original works relating primarily to neurosurgery, including studies in clinical neurophysiology, organic neurology, ophthalmology, radiology, pathology, and molecular biology. The Editors and Editorial Boards encourage submission of clinical and laboratory studies. Other manuscripts accepted for review include technical notes on instruments or equipment that are innovative or useful to clinicians and researchers in the field of neuroscience; papers describing unusual cases; manuscripts on historical persons or events related to neurosurgery; and in Neurosurgical Focus, occasional reviews. Letters to the Editor commenting on articles recently published in the Journal of Neurosurgery, Journal of Neurosurgery: Spine, and Journal of Neurosurgery: Pediatrics are welcome.
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