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Keywords = unilateral basal ganglia calcinosis

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11 pages, 6644 KiB  
Case Report
A Forgotten Rare Cause of Unilateral Basal Ganglia Calcinosis Due to Venous Angioma and Complicating Acute Stroke Management: A Case Report
by Arturs Balodis, Sintija Strautmane, Oskars Zariņš, Kalvis Verzemnieks, Jānis Vētra, Sergejs Pavlovičs, Edgars Naudiņš and Kārlis Kupčs
Diagnostics 2025, 15(3), 291; https://doi.org/10.3390/diagnostics15030291 - 26 Jan 2025
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Abstract
Background: Unilateral basal ganglia calcinosis (BGC) is a rare radiological finding that can be diagnosed on computed tomography (CT) and magnetic resonance imaging (MRI) but often presents challenges for clinicians and radiologists in determining its underlying cause. So far, only a few potential [...] Read more.
Background: Unilateral basal ganglia calcinosis (BGC) is a rare radiological finding that can be diagnosed on computed tomography (CT) and magnetic resonance imaging (MRI) but often presents challenges for clinicians and radiologists in determining its underlying cause. So far, only a few potential causes that could explain unilateral BGC have been described in the literature. Case Report: A 54-year-old Caucasian male was admitted to a tertiary university hospital due to the sudden onset of speech impairment and right-sided weakness. The patient had no significant medical history prior to this event. Non-enhanced computed tomography (NECT) of the brain revealed no evidence of acute ischemia; CT angiography (CTA) showed acute left middle cerebral artery (MCA) M2 segment occlusion. CT perfusion (CTP) maps revealed an extensive penumbra-like lesion, which is potentially reversible upon achieving successful recanalization. However, a primary neoplastic tumor with calcifications in the basal ganglia was initially interpreted as the potential cause; therefore, acute stroke treatment with intravenous thrombolysis was contraindicated. A follow-up CT examination at 24 h revealed an ischemic lesion localized to the left insula, predominantly involving the left parietal lobe and the superior gyrus of the left temporal lobe. Subsequent gadolinium-enhanced brain MRI revealed small blood vessels draining into the subependymal periventricular veins on the left basal ganglia. Digital subtraction angiography was conducted, confirming the diagnosis of venous angioma. Conclusions: Unilateral BGC caused by venous angioma is a rare entity with unclear pathophysiological mechanisms and heterogeneous clinical presentation. It may mimic conditions such as intracerebral hemorrhage or hemorrhagic brain tumors, complicating acute stroke management, as demonstrated in this case. Surrounding tissue calcification may provide a valuable radiological clue in diagnosing venous angiomas DVAs and vascular malformations. Full article
(This article belongs to the Special Issue Advances in Cerebrovascular Imaging and Interventions)
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Figure 1

Figure 1
<p>(<b>A</b>) Non-enhanced computed tomography of the brain showing a hyperdense artery sign, arteria cerebri media sin. M1 segment (red arrow). The hyperdense artery sign typically indicates acute thrombosis, especially in the presence of corresponding neurological symptoms. (<b>B</b>) Non-enhanced computed tomography of the brain at the basal ganglia level shows unilateral basal ganglia calcinosis, predominantly in the caput nuclei caudati and nucleus lentiforme (red arrow), without perifocal edema or mass effect, suggesting changes in a more likely benign nature. (<b>C</b>) Computed tomography post-contrast on left basal ganglia level in axial and sagittal planes showing a low contrast enhancement vessel venous angioma, which corresponds to developmental venous anomaly (DVA) and is regarded as the underlying cause of basal ganglia calcinosis (red circle and red arrow). (<b>D</b>) Retrospective analysis of the computed tomography angiography (MIP-CTA) images, performed before the MRI and DSA examinations, reveals a small venous angioma (DVA) in the left basal ganglia (red arrows).</p>
Full article ">Figure 2
<p>Computed tomography perfusion (CTP) after contrast injection shows a large hypoperfusion area in the territory of the left middle cerebral artery (ACM sin) with extensive penumbra-type damage (salvageable brain tissue) and a small core-type lesion in the parietal lobe, comprising less than one-third of the total hypoperfusion volume. The findings suggest the patient could potentially benefit from intravenous thrombolysis. Cerebral blood flow (CBF) 9%; cerebral blood volume (CBV) 23%; mean transit time (MTT) 237%.</p>
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<p>At 1 day post-admission, a magnetic resonance imaging (MRI) with fluid-attenuated inversion recovery (FLAIR) and T2-weighted sequences reveals acute ischemia in the left insula and left parietal lobe, and upper gyrus of temporal lobe corresponding to the lesion seen on CTP and consistent with the territory of the left middle cerebral artery (MCA), M2 segment (red arrows). Diffusion-weighted imaging (DWI) sequence showing restricted diffusion on left side insula, left parietal, and temporal lobe with low apparent diffusion coefficient (ADC) map value, which corresponds to acute infarction of the middle cerebral artery territory of the left side M2 occlusion (red arrows).</p>
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<p>Digital subtraction angiography in LL projection at the level of basal ganglia showing abnormal vessels, which corresponds to developmental venous anomaly angioma in the left area of the basal ganglia, also these changes are seen on CTA and MRI after contrast injection (red arrow).</p>
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