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Table of Contents
LETTER TO THE EDITOR
Year : 2023  |  Volume : 26  |  Issue : 1  |  Page : 87-88
 

Pure Arterial Malformation (PAM): Case report and review of literature


1 Division of Medicine, Health Sciences North, Northern Ontario School of Medicine, 41, Ramsey Lake Road, Sudbury, ON- P3E 6J1, Canada
2 Division of Neurology, Department of Medicine, Sunnybrook Health Sciences Centre, Temerty School of Medicine, University of Toronto, EG41 2075 Bayview Ave, Toronto, ON, M4N 3M5, Canada
3 Division of Neurology, Neurosurgery, and Diagnostic Imaging, Hamilton General Hospital, McMaster University, 237 Barton St E, Hamilton, Canada, ON L8L 2X2, Canada

Date of Submission28-Sep-2022
Date of Decision07-Nov-2022
Date of Acceptance17-Nov-2022
Date of Web Publication04-Jan-2023

Correspondence Address:
Aviraj S Deshmukh
Division of Medicine, Health Sciences North, Northern Ontario School of Medicine, 41, Ramsey Lake Road, Sudbury, Toronto, ON- P3E 6J1
Canada
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Source of Support: None, Conflict of Interest: None


DOI: 10.4103/aian.aian_797_22

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How to cite this article:
Deshmukh AS, Hawkes C, Adel BV. Pure Arterial Malformation (PAM): Case report and review of literature. Ann Indian Acad Neurol 2023;26:87-8

How to cite this URL:
Deshmukh AS, Hawkes C, Adel BV. Pure Arterial Malformation (PAM): Case report and review of literature. Ann Indian Acad Neurol [serial online] 2023 [cited 2023 Feb 1];26:87-8. Available from: https://www.annalsofian.org/text.asp?2023/26/1/87/367047




Dear Editor,

Pure arterial malformations (PAMs) are defined as dilated, overlapping, and tortuous arteries and/or a mass of arterial loops without arteriovenous (AV) shunting. The term pure arterial malformation (PAM) was first described in 2013 by McLaughlin et al.,[1] and since then only a few cases have been reported. The etiology, natural history, and treatment strategies of PAM have not been fully elucidated. We describe a case of PAM involving the left anterior cerebral anterior cerebral circulation (ACA and MCA).

A male in his mid-sixties underwent vascular imaging for a recently diagnosed left medial frontal and left occipital meningiomas. Cranial CT angiography (CTA) and digital subtraction angiography (DSA) demonstrated vascular abnormalities involving the left ACA and MCA. The left ACA showed a dysplastic, dilatated, and tortuous vessel with a redundant A2 and proximal A3 segment of the left ACA, angioarchitecture consistent with a PAM [Figure 1]. The left ACA showed a mass of arterial loops without evidence of AV shunting or aneurysmal dilatation. In addition, the proximal M1 segment and the M2 bifurcation segments are dysplastic with surrounding calcifications [Figure 1].
Figure 1: Representative case with cranial CTA and DSA demonstrating a pure arterial malformation involving the left anterior cerebral circulation. (a and b) CTA axial and sagittal (MIP) image showing tortuosity and arterial loops involving the left A2 ACA, proximal A3, and left M1 segment of the MCA with surrounding calcification (white arrow). (c-f) 2D DSA image (AP and lateral view, black arrow), and 3D DSA image (AP and Lateral view, Star sign *) showing pure arterial malformation involving ACA and MCA. (g and h) Venous phase of 2D DSA (AP and lateral view) showing normal venous draining pattern

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Pure arterial malformations are a recently described intracranial vascular abnormality that are commonly mistaken for aneurysms or arteriovenous malformations (AVM) on non-invasive imaging. They are characterized by the absence of any venous component, thus, clearly differentiating PAM intracranial vascular malformations with AV shunting like AVMs. In addition, PAM can be erroneously labeled as a dolichoectasia. But dolichoectasia predominantly involves the vertebrobasilar system and/or internal cerebral artery and rarely involves distal vessels.[2] Dolichoectatic vessels are elongated, dilated, and sometimes tortuous, although they are still recognizable, whereas with PAM the tortuosity is often so severe that the vessel has the appearance of a mass or cluster of arterial loops. The pathomechanism of dolichoectasia can be divided into the following subtypes: atherosclerotic, non-atherosclerotic, or associated with an arterial dissection. The vast majority of dolichoectasia are due to atherosclerotic, and these patients tend to be older males with a history of vascular comorbidities such as hypertension and smoking. The non-atherosclerotic variants are typically seen in younger patients with underlying connective tissue disorders.[2] The incidence of PAM is very low with few cases reported in the literature[3],[4] and typically seen in young adult females, with male-to-female ratio of 1:3.[4] The majority of PAM cases are clinically asymptomatic and reported as an incidental finding with only a single case report of a symptomatic PAM.[4] Although any intracranial vessels can be involved, there is a predilection for anterior cerebral artery (ACA) and posterior cerebral artery (PCA).[5] Involvement of the ACA involves distal A2 and A3 segments with surrounding calcification.[5] Catheter angiography is essential for the diagnosis as it provides the temporal and spatial resolution necessary to exclude AV shunting and to discern the angioarchitecture of the tightly coiled arterial loops.

The exact etiology of pure arterial malformations is unknown; however, possible pathogenic mechanisms include congenital insult or somatic mutation later in life, underlying connective tissue disorder, post-infectious and/or a chronic healed arterial dissection.[5] Cortical or white matter dysplasia in the area supplied by the PAM has been noted in the literature pointing toward a congenital etiology, at least in a few cases detected in childhood.[6] Chronic calcifications associated with PAM suggest a long-standing pathological process prior to the ultimate diagnosis. Indeed, early childhood viral injection has been implicated as a possible etiology of PAM.[5],[7]

Our case showed PAM involving the left anterior cerebral circulation. The associated calcifications would suggest a long-standing lesion that likely occurred at a much younger age. Similar to the majority of cases published to date, the PAM in our patient was clinically asymptomatic and he underwent successful surgical treatment of his meningioma. Unlike other malformations, PAM has a more benign natural history and is generally managed conservatively. We believe that pure arterial malformations are likely more common than reported, and their understanding is important for diagnosis and appropriate patient counseling. Further, studies on the etiologies, predisposing factors, genetic association, and treatment strategies for PAMs are needed.

Financial support and sponsorship

Nil.

Conflicts of interest

There are no conflicts of interest.



 
   References Top

1.
McLaughlin N, Raychev R, Duckwiler G, Martin NA. Pure arterial malformation of the posterior cerebral artery: Importance of its recognition. J Neurosurg 2013;119:655-60.  Back to cited text no. 1
    
2.
Pico F, Labreuche J, Amarenco P. Pathophysiology, presentation, prognosis, and management of intracranial arterial dolichoectasia. Lancet Neurol 2015;14:833-45.  Back to cited text no. 2
    
3.
Liu TY, Xu N, Wan Z, Zhang ZM, Xu JJ, Meng H, et al. Diagnosis and treatment of pure arterial malformation: Three case reports and literature review. Medicine (Baltimore) 2020;99:e20229.  Back to cited text no. 3
    
4.
Yue H, Ling W, Hanmin C, Yibo O, Po Z, Dongsheng G, et al. Progressive pure arterial malformations of the anterior cerebral artery. World Neurosurg 2019;131:e52-64.  Back to cited text no. 4
    
5.
Brinjikji W, Cloft HJ, Flemming KD, Comelli S, Lanzino G. Pure arterial malformations. J Neurosurg 2018;129:91-9.  Back to cited text no. 5
    
6.
Baccin CE, Krings T, Alvarez H, Ozanne A, Lasjaunias PL. A report of two cases with dolichosegmental intracranial arteries as a new feature of PHACES syndrome. Childs Nerv Syst 2007;23:559-67.  Back to cited text no. 6
    
7.
Lasjaunias PL. Segmental identity and vulnerability in cerebral arteries. Interv Neuroradiol 2000;6:113-24.  Back to cited text no. 7
    


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