Perivascular spaces, also known as Virchow-Robin spaces, are pial-lined interstitial fluid-filled spaces in the brain that surround perforating vessels. They do not have a direct connection with the subarachnoid space and in fact, the fluid within them is a slightly different composition as compared to CSF.
On axial imaging, they appear as smoothly demarcated fluid-filled cysts, typically less than 5 mm in diameter, showing the same attenuation or intensity as CSF, and often found in the basal ganglia or midbrain.
When perivascular spaces are very large, they are referred to as tumefactive perivascular spaces.
When located in the anterior temporal lobe and related to a vascular loop, they are known as anterior temporal lobe perivascular spaces; however, these likely represent a different entity compared to typical scattered perivascular spaces.
Perivascular spaces are very common, and increasingly seen with better MRI image resolution. Depending on defining criteria, they are seen in 50-100% of patients 2,3.
They are almost invariably asymptomatic, even when quite large. Rarely, they can cause mass effect and can result in obstructive hydrocephalus.
Perivascular spaces are normal structures which consist of a single or double layer of invaginated pia surrounding small cerebral blood vessels 8,14. They are mostly microscopic, although more enlarged spaces may be detected on CT or MRI 14.
Perivascular spaces which are visible on imaging are typically less than 5 mm in diameter, but can reach much larger sizes. A so-called "giant" perivascular space or tumefactive perivascular space, and can exert enough mass effect to be symptomatic 1. They tend to enlarge with age and hypertension.
Previously, perivascular spaces were believed to be entirely incidental findings, mostly significant so as not to be mistaken for a more sinister pathology. This is especially true with a tumefactive or unusual in appearance (e.g. anterior temporal lobe perivascular spaces which are often mistaken for tumours).
More recently, a few studies have suggested an association between between extensive basal ganglia perivascular spaces (état criblé) and changes of chronic microvascular ischaemic disease 12-14. This is related to the observation that, although a few scattered perivascular spaces are a nearly ubiquitous imaging finding, the number and prominence of these spaces increases with aging and along with other findings of microvascular disease, e.g. periventricular white matter lesions and lacunar infarctions. The association remains controversial 14.
Most commonly, perivascular spaces are located in the lower half of the basal ganglia, especially in the anterior perforated substance along the line of the anterior commissure 3. They are also found in 1:
- substantia nigra
- dentate nucleus
- subinsular region: "subinsular bright spots"
- corpus callosum and cingulate gyrus
The cortical regions are spared. In contrast to lacunar infarcts encountered more frequently in the upper half of the putamen, perivascular spaces are seen more often in the lower half.
A special type of perivascular space occurs in the anterior temporal lobe and can mimic a cystic tumour. These are discussed separately: anterior temporal lobe perivascular spaces 9,10.
Perivascular spaces are divided into three main types 4:
- type 1: located in the area supplied by the lenticulostriate arteries entering the basal ganglia
- type 2: located in the area supplied by the perforating medullary arteries as they enter the cortical grey matter
- type 3: located in the midbrain
They are usually idiopathic, although they are seen in greater frequency in 1,4,11:
- mucopolysaccharidoses, e.g. Hunter disease, Hurler disease
- some muscular dystrophies
- traumatic brain injury
- hypertensive angiopathy 12
- cerebral amyloid angiopathy
As they are filled with a fluid similar to CSF, perivascular spaces have appearances akin to water on all imaging modalities and sequences. Differentiating them from foci of encephalomalacia that result from chronic lacunar infarcts can be challenging but is important as imaging findings of ischaemia can lead to patients being put on medication such as antiplatelet therapy.
Perivascular spaces should be considered if:
- patient is young
- absence of vascular risk factors
- no other changes of chronic small vessel ischaemia.
- well-circumscribed fluid-density spaces
- no enhancement
- no calcification
- CT angiography occasionally demonstrates a traversing vessel
They follow CSF signal on all pulse sequences 7. When small, the adjacent white matter is normal, thus helping to distinguish perivascular spaces from lacunar infarcts, which have surrounding gliosis (best seen on T2 FLAIR sequence).
Although generally cyst-like on axial sequences, on sagittal and coronal sequences a linear radiating morphology may be seen consistent with their role in surrounding vessels.
In a minority of cases, especially when they are large, a thin increased T2-signal halo may be seen. Usually, they will have a positive mass effect. On T2 sequences, a traversing vessel is sometimes seen.
The exception to the 'no surrounding high T2 signal' rule is are anterior temporal lobe perivascular spaces 9,10.
History and etymology
Virchow-Robin spaces are named after German pathologist Rudolf Virchow (1821–1902) and French anatomist Charles Philippe Robin (1821–1885).
For small perivascular spaces, consider:
- choroid fissure cyst
lacunar infarcts and striatocapsular infarcts
- a rim of gliosis seen best on FLAIR 8
- neutral or negative mass effect
- typically upper two-thirds of basal ganglia (due to infarcts of perforating end arteries)
chronic small vessel ischaemic disease
- typically periventricular and subcortical
- cyst with a dot sign
- CNS cryptococcosis: if multiple
For giant perivascular spaces consider:
- 1. Salzman KL, Osborn AG, House P et-al. Giant tumefactive perivascular spaces. AJNR Am J Neuroradiol. 2005;26 (2): 298-305. AJNR Am J Neuroradiol (full text) - Pubmed citation
- 2. Song CJ, Kim JH, Kier EL et-al. MR imaging and histologic features of subinsular bright spots on T2-weighted MR images: Virchow-Robin spaces of the extreme capsule and insular cortex. Radiology. 2000;214 (3): 671-7. Radiology (full text) - Pubmed citation
- 3. Jungreis CA, Kanal E, Hirsch WL et-al. Normal perivascular spaces mimicking lacunar infarction: MR imaging. Radiology. 1988;169 (1): 101-4. Radiology (abstract) - Pubmed citation
- 4. Kwee RM, Kwee TC. Virchow-Robin spaces at MR imaging. Radiographics. 2007;27 (4): 1071-86. doi:10.1148/rg.274065722 - Pubmed citation
- 5. Ogawa T, Okudera T, Fukasawa H et-al. Unusual widening of Virchow-Robin spaces: MR appearance. AJNR Am J Neuroradiol. 1995;16 (6): 1238-42. Pubmed citation
- 6. Papayannis CE, Saidon P, Rugilo CA et-al. Expanding Virchow Robin spaces in the midbrain causing hydrocephalus. AJNR Am J Neuroradiol. 2003;24 (7): 1399-403. Pubmed citation
- 7. Brant WE, Helms CA. Fundamentals of Diagnostic Radiology. Lippincott Williams & Wilkins. (2007) ISBN:0781761352. Read it at Google Books - Find it at Amazon
- 8. Osborn AG, Preece MT. Intracranial cysts: radiologic-pathologic correlation and imaging approach. Radiology. 2006;239 (3): 650-64. Radiology (full text) - doi:10.1148/radiol.2393050823 - Pubmed citation
- 9. Rawal S, Croul SE, Willinsky RA et-al. Subcortical cystic lesions within the anterior superior temporal gyrus: a newly recognized characteristic location for dilated perivascular spaces. AJNR Am J Neuroradiol. 2014;35 (2): 317-22. doi:10.3174/ajnr.A3669 - Pubmed citation
- 10. Lim AT, Chandra RV, Trost NM et-al. Large anterior temporal Virchow-Robin spaces: unique MR imaging features. Neuroradiology. 2015;57 (5): 491-9. doi:10.1007/s00234-015-1491-y - Pubmed citation
- 11. Inglese M, Bomsztyk E, Gonen O et-al. Dilated perivascular spaces: hallmarks of mild traumatic brain injury. AJNR Am J Neuroradiol. 2005;26 (4): 719-24. AJNR Am J Neuroradiol (full text) - Pubmed citation
- 12. Loos CM, Klarenbeek P, van Oostenbrugge RJ, Staals J. Association between Perivascular Spaces and Progression of White Matter Hyperintensities in Lacunar Stroke Patients. (2015) PloS one. 10 (9): e0137323. doi:10.1371/journal.pone.0137323 - Pubmed
- 13. Doubal FN, MacLullich AM, Ferguson KJ, Dennis MS, Wardlaw JM. Enlarged perivascular spaces on MRI are a feature of cerebral small vessel disease. (2010) Stroke. 41 (3): 450-4. doi:10.1161/STROKEAHA.109.564914 - Pubmed
- 14. Shi Y, Wardlaw JM. Update on cerebral small vessel disease: a dynamic whole-brain disease. (2016) Stroke and vascular neurology. 1 (3): 83-92. doi:10.1136/svn-2016-000035 - Pubmed