Evidence map›Paper›PMID 40837290›Full record

ArticleSurgical neurology international2025

Probable cerebral amyloid angiopathy-related inflammation presenting with dissociated hemorrhagic and inflammatory lesions in a middle-aged patient: A case report.

Toshihide Takahashi, Kiyoyuki Yanaka, Hitoshi Aiyama, Minami Saura, Hayato Takeda, Nobuyuki Takahashi, Aiki Marushima, Eiichi Ishikawa

Abstract readCase Reports
In one paragraph

Article in Surgical neurology international, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Toshihide TakahashiDepartment of Neurosurgery, Tsukuba Memorial Hospital, Tsukuba City, Japan.
Kiyoyuki YanakaDepartment of Neurosurgery, Tsukuba Memorial Hospital, Tsukuba City, Japan.
Hitoshi AiyamaDepartment of Neurosurgery, Tsukuba Memorial Hospital, Tsukuba City, Japan.
Minami SauraDepartment of Neurosurgery, Tsukuba Memorial Hospital, Tsukuba City, Japan.
Hayato TakedaDepartment of Neurology, Tsukuba Memorial Hospital, Tsukuba City, Japan.
Nobuyuki TakahashiDepartment of Radiology, Tsukuba Memorial Hospital, Tsukuba City, Japan.
Aiki MarushimaDepartment of Neurosurgery, Faculty of Medicine, University of Tsukuba, Tsukuba City, Japan.
Eiichi IshikawaDepartment of Neurosurgery, Faculty of Medicine, University of Tsukuba, Tsukuba City, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Cerebral amyloid angiopathy-related inflammation (CAA-ri) is a rare inflammatory encephalopathy associated with amyloid-β deposition in cerebral vessels, typically presenting in older adults with subacute cognitive decline, seizures, and lobar hemorrhages. It affects approximately 5% of patients with CAA, often showing asymmetric white matter hyperintensities, microbleeds, and leptomeningeal enhancement on magnetic resonance imaging (MRI). Vascular fragility in patients with CAA-ri increases rebleeding risk compared with those without CAA-ri, such as those with hypertensive intracerebral hemorrhage. This report describes a rare probable CAA-ri case in a middle-aged patient with an atypical presentation: younger age, absence of typical inflammatory symptoms, and spatially dissociated hemorrhagic and inflammatory lesions. Case Description: A 50-year-old man with a history of childhood right frontal hemorrhage and epilepsy presented with right upper-limb numbness. Computed tomography revealed a left parietal subcortical hemorrhage, and MRI showed bilateral occipital white matter hyperintensities, microbleeds, and right occipital leptomeningeal enhancement. Biopsy of the right occipital lesion confirmed amyloid-β deposition with mild perivascular lymphocytic infiltration, indicating probable CAA-ri. He was managed conservatively owing to the minimal mass effect and received corticosteroids as outpatients. MRI at 19 months revealed resolution of occipital hyperintensities, without neurological deficits. Conclusion: This case highlights probable CAA-ri in a middle-aged adult, presenting with subcortical hemorrhage and spatially dissociated inflammatory lesions. Despite the subtle inflammatory findings, clinical, imaging, and histological evaluations supported the diagnosis. Early recognition and immunosuppressive therapy can achieve favorable outcomes, emphasizing CAA-ri's inclusion in the differential diagnosis of lobar hemorrhage in relatively younger patients without hypertension or vascular risk factors.

Indexed as

BiopsyCerebral amyloid angiopathyInflammationIntracerebral hemorrhageMagnetic resonance imaging

Identifiers

PMID40837290
PMCPMC12361660

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.