| 词条 | Leptomeningeal collateral circulation | ||||||||||||||||||||||||||||||||
| 释义 |
The leptomeningeal collateral circulation (also known as leptomeningeal anastomoses or pial collaterals) is a network of small blood vessels in the brain that connects branches of the middle, anterior and posterior cerebral arteries (MCA, ACA, and PCA).[1] StructureLeptomeningeal collaterals lie within the leptomeninges, the two deep layers of the meninges called the pia mater and the arachnoid mater.[2] Their diameter has been measured at approximately 300 micrometers,[3] but there is variability between individuals in the size, quantity and location of these vessels, and between either hemisphere within the same subject.[4] Inter-territorial end to end anastomoses exist between branches of the ACA and MCA, the PCA and MCA, the ACA and PCA, and the right and left ACAs.[4][5][6][7] Intra-territorial anastamoses connect adjacent arterial branches within the same arterial territory (between two branches of the same MCA, for example).[3]
Inter-territorial leptomeningeal anastamoses between the PCA and ACA have been observed between the parieto-occipital branch of the PCA, and the precuneal branch or the posterior pericallosal branch of the ACA.[1] Inter-territoral leptomeningeal anastamoses between the right and left ACAs have been observed between the right and left pericallosal arteries and the right and left callosal marginal arteries. Anastamoses have also been observed between precuneal branches originating from the middle portion of the pericallosal artery, or from the posterior portion of the callosal marginal branch of one side joining the opposite paracentral branch.[1] FunctionLeptomeningeal collateral vessels allow limited cerebral blood flow and brain tissue perfusion when normal circulation through the circle of Willis is impaired, through a series of anastomotic connections between cerebral arteries.[8] Clinical significanceStrokeDuring an ischaemic stroke, blood flow through a cerebral artery is compromised. This frequently causes substantial injury to the area of the brain supplied by the artery, but not all of this territory is necessarily affected. A post mortem study of MCA strokes demonstrated that the area of brain injury was often smaller than the total area supplied by the MCA. Leptomeningeal collateral vessels from the ACA and PCA appeared to allow for perfusion of some brain tissue to persist, partially compensating for the loss of the major vessel.[9] This compensatory effect is however usually inadequate to maintain a normal blood supply.[10] There is anatomical variation in collateral circulation from person to person, and as we age, collateral vessels decrease in diameter and number. Therapies that attempt to optimize leptomeningeal collateral circulation appear to improve outcomes following acute ischaemic stroke.[11] MRI and CT brain imaging is used to determine the severity of a stroke, and help guide treatment. Fluid attenuated inversion recovery (FLAIR) vascular hyperintensity (FVH) is a radiographic marker seen on brain imaging in acute ischaemic stroke. FVH can be used as a proxy for slow leptomeningeal collateral blood flow, and may help reveal which areas of brain tissue are potentially salvagable.[12]Alzheimer’s diseaseThe age-related changes that can be seen in leptomeningeal vessels over time appear to be accelerated by Alzheimer's disease, according to mouse models conducted in 2018.[13] Intracranial haemorrhageA 2016 study compared patients awaiting carotid artery stenting for unilateral atherosclerotic plaques. Those with leptomenigneal collaterals evident on cranial angiography had a higher incidence of intracranial haemorrhage (ICH) after stenting. The authors argued that the presence of such collaterals on imaging should be considered a risk factor for ICH in patients where carotid stenting is otherwise indicated.[14] HistoryThe term 'leptomeningeal' derives from the Greek word leptos (λεπτός) meaning thin, in reference to the appearance of the pia mater and arachnoid mater. Descriptions of leptomenigeal collateral vessels are found in Thomas Willis’ Cerebri Anatome (1664).[15][16] German physician Otto Heubner first demonstrated their presence in his 1874 work Die luetische Erkrankung Der Hirnaterien.[17] He injected the MCA, ACA and PCA in turn, in an attempt to establish the territories these arteries supply. Even when other anastomoses from the circle of Willis were blocked off, the whole cerebral arterial tree could be filled.[1] Later study in the 1950s and 60s by H.M. Vander Eecken and R.D. Adams provided a comprehensive review of the anatomy of the leptomeningeal collateral circulation.[9] The concept of the ischaemic penumbra, where brain tissue shows capacity to recover if perfusion is quickly restored, was defined in 1981 by Astrup et al. Persistent blood flow through leptomeningeal vessels is a key part of this recovery.[18] Other animalsHaemodynamic studies of leptomeningeal collaterals have been conducted in primates.[19] Leptomeningeal circulation has been observed in mice and rats during experiments to assess changes associated with disease and ageing in these vessels.[20] References1. ^1 2 3 {{Cite journal|last=Brozici Mariana|last2=van der Zwan Albert|last3=Hillen Berend|date=2003-11-01|title=Anatomy and Functionality of Leptomeningeal Anastomoses|journal=Stroke|volume=34|issue=11|pages=2750–2762|doi=10.1161/01.STR.0000095791.85737.65|pmid=14576375}} 2. ^{{Cite journal|last=Patel|first=Neel|last2=Kirmi|first2=Olga|date=2009|title=Anatomy and imaging of the normal meninges|journal=Seminars in Ultrasound, CT, and MR|volume=30|issue=6|pages=559–564|issn=0887-2171|pmid=20099639|doi=10.1053/j.sult.2009.08.006}} 3. ^1 2 {{Cite journal|last=Phan|first=Thanh G.|last2=Hilton|first2=James|last3=Beare|first3=Richard|last4=Srikanth|first4=Velandai|last5=Sinnott|first5=Matthew|date=2014-09-19|title=Computer Modeling of Anterior Circulation Stroke: Proof of Concept in Cerebrovascular Occlusion|url=http://journal.frontiersin.org/article/10.3389/fneur.2014.00176/abstract|journal=Frontiers in Neurology|volume=5|doi=10.3389/fneur.2014.00176|issn=1664-2295}} 4. ^{{Cite book|url=https://www.ncbi.nlm.nih.gov/books/NBK53086/|title=Anatomy and Ultrastructure|last=Cipolla|first=Marilyn J.|date=2009|publisher=Morgan & Claypool Life Sciences|language=en}} 5. ^{{Cite journal|last=Türe|first=Uğur|last2=Yaşargil|first2=M. 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