Central nervous system vasculitis

More documents

Recommendations

Info

Central nervous system vasculitis Hajj-Ali and Calabrese 11cases. Recently, the term reversible cerebral vasoconstrictionsyndrome (RCVS) was proposed to comprise agroup of disorders characterized by acute onset of headaches,with or without neurologic deficit, and prolongedbut reversible cerebral vasoconstriction. RCVS are confinedto the CNS but has marked clinical and pathophysiologicalheterogeneity than GACNS. Being a majormimic of PACNS, RCVS will be discussed in the sectionof primary central nervous system vasculitis. However, itcannot be overemphasized that RCVS is not a form oftrue CNS vasculitis, but rather a group of vasoconstrictivesyndromes.Granulomatous angiitis of the central nervous systemGACNS represents about 20% of all patients withPACNS. It appears to be male-predominant and occursat any age. It is characterized by a long prodromal period,with few patients presenting acutely. Signs and symptomsof systemic vasculitis such as peripheral neuropathy,fever, weight loss, or rash are usually lacking. Because thevasculitis may affect any area of the CNS, its presentationmay vary widely, and no set of clinical signs is specificfor the diagnosis. Signs and symptoms of GACNS aresummarized below:(1) Chronic headaches.(2) Encephalopathy.(3) Strokes/transient ischemic attack (more commonrecurrent).(4) Seizures.(5) Behavioral and cognitive changes.(6) Focal motor/sensory abnormalities.(7) Ataxia.(8) Myelopathy.GACNS may be suspected in the setting of chronicmeningitis, recurrent focal neurologic symptoms, unexplaineddiffuse neurologic dysfunction, or unexplainedspinal cord dysfunction not associated with systemicdisease or any other process.The characteristic pathologic findings include classicgranulomatous angiitis affecting the small and mediumleptomeningeal and cortical arteries with Langhansor foreign body giant cells, necrotizing vasculitis, or alymphocytic vasculitis. The inflamed vessels becomenarrowed, occluded, and thrombosed, causing tissueischemia and necrosis of the territories of the involvedvessels.The primary event that elicits the inflammatoryprocess in GACNS remains unknown. It is possible thataltered host defense mechanisms tilt the balance ofthe immune system and allow a viral illness to escapethe immune system, which sets off the vasculitic process[3–8].Reversible cerebral vasoconstriction syndromesBenign angiopathy of the CNS (BACNS) was initiallyproposed as a term to characterize a distinct subset ofpatients with isolated neurologic events, characterized byfemale predominance, acute presentation, reversibleangiographic abnormalities, normal results on spinal fluidexamination, and monophasic course [9]. The term‘angiopathy’ was used because of uncertainty regardingthe nature of the pathologic process affecting the vesselwall and the lack of evidence of blood vessel inflammation.In 2002, Hajj-Ali et al. [10] described dramaticresolution of angiographic abnormalities in series of 16patients within 4–12 weeks without intensive immunosuppressivetherapy. With these data, it became apparentthat the underlying pathophysiologic disorder in BACNSpatients was reversible vasoconstriction rather than vasculitis.Further on, the term BACNS evolved into a newterminology referred to as reversible cerebral vasoconstrictionsyndromes. The evolvement in the terminologyto RCVS occurred with the recognition that RCVS comprisea group of diverse conditions, all characterized byreversible multifocal narrowing of the cerebral arteriesheralded by sudden, severe (thunderclap) headacheswith or without associated neurologic deficits and mostimportantly by reversible angiographic findings. RCVSinclude BACNS, Call–Fleming syndrome, postpartumangiopathy, migrainous vasospasm, and drug-induced‘arteritis’ [11 ]. Calabrese et al. [11 ] proposed criticalelements for the diagnosis of RCVS which are summarizedbelow.(1) Transfemoral angiography or indirect computed tomographyangiography (CTA) or magnetic resonanceangiography (MRA) documenting multifocal segmentalcerebral artery vasoconstriction.(2) No evidence for aneurysmal subarachnoid hemorrhage.(3) Normal or near-normal cerebrospinal fluid analysis(protein level
12 Vasculitis syndromesTable 1 Comparison of clinical and diagnostic characteristics of reversible cerebral vasoconstriction syndromes and granulomatousangiitis of the central nervous systemRCVSGACNSPatients Female predominant Male predominantHeadaches Acute Chronic, insidiousCSF findings Normal to near-normal AbnormalAngiographyDiffuse areas of multiple stenoses and dilatationinvolving intracranial cerebral arteries, whichare reversible within 6–12 weeksCNS biopsy No vasculitic changes Granulomatous angiitisFrequently normal; otherwise, findings range from singleor multiple arterial cut-off areas, to luminal irregularitiesin single or multiple arteries, to diffuse abnormalities thatare occasionally indistinguishable from RCVS. Theseabnormalities are frequently irreversibleCNS, central nervous system; CSF, cerebrospinal fluid; GACNS, granulomatous angiitis of the central nervous system; RCVS, reversible cerebralvasoconstriction syndrome. Adapted with modification from [11 ] with permission.the control of cerebral vascular tone seems to be thecritical element in the pathophysiology of RCVS[10,13 ]. In support of this hypothesis is the dearth ofinflammatory changes in CNS pathology of patients withRCVS. Our recent report [13 ] of the largest series ofRCVS to date included 120 patients, 21 of whom underwentbrain biopsies. None of these biopsies revealed anyvasculitic changes. In addition, 98% of the follow-upvascular imaging in this series revealed partial or fullreversibility of the initial vascular abnormalities.The alteration in vascular tone in RCVS may be spontaneousor evoked by various exogenous or endogenousfactors. Exogeneous factors include sympathomimetic orserotonergic drugs [14–20], and direct or neurosurgicaltrauma [21–23]. Endogenous factors include serotonergictumors and uncontrolled hypertension [24].Primary angiitis of the central nervous system:atypical casesMost PACNS patients present atypically. This subsetdoes not fit the diagnostic features for either GACNS orRCVS, yet these patients demonstrate angiographic orhistopathologic evidence of PACNS. Included in thisTable 2 Clinical and radiographic data in 67 patients withreversible cerebral vasoconstriction syndromeAge 42.5 (range 19–70)Female/male 43/24Precipitating factorNone 25 (37%)Postpartum 5 (8%)Vasoactive substance 37 (55%)Headaches 67 (100%)Recurrent thunderclap 63 (94%)Single thunderclap 3 (4.5%)Recurrent severe 1 (1.5%)Focal neurological deficits 14 (21%)Seizures 2 (3%)Abnormal brain MRI 19 (28%)cSAH 15 (22%)Silent infarct 1 (1%)RPLS 6 (9%)cSAH, cortical subarachnoid hemorrhage; RPLS, reversible posteriorleukoencephalopathy. Adapted with permission from [12 ].group are patients with abnormal cerebrospinal fluid(CSF) findings that preclude a diagnosis of RCVSor those with GACNS-like presentation but withoutgranulomatous features on CNS biopsies. In addition,patients presenting with PACNS at unusual anatomicsites such as the spinal cord or those presenting with masslesions are included in this category.Secondary central nervous system vasculitisSecondary CNS vasculitis has been described in associationwith multiple conditions including systemic vasculitides,connective tissue disease (CTD), sarcoidosis,infections, and lymphoproliferative diseases. CNS involvementin these setting is frequently a presumed diagnosis,on the basis of radiographic rather than pathologicmodalities.Infectious causes of central nervous system vasculitisInfections affecting the CNS are great mimickers ofPACNS. The infection may be occult and a high degreeof suspicion coupled with the epidemiologic features andthe individual risk factors are important features in theworkup of patients with possible PACNS. In the workupof patients for possible PACNS, it is imperative to searchfor an infectious process through CSF or pathologicexamination, even when a vasculitic process is establishedby pathologic basis. The possibility of infectionswith human immunodeficiency virus (HIV), Varicellazoster (VZV), or syphilis should be actively identified.VZV-associated cerebral angiitis affects older age groups[25] and the disease tends to be more localized thanPACNS as well as less severe. The known antecedentinfection with herpes zoster suggests the underlyingcause. Cerebral angiographic findings of segmental, unilateralinvolvement of the vessels in the distribution ofthe middle cerebral artery and, occasionally, the internalcarotid artery are characteristic findings in VZV angiitis.The diagnosis is confirmed by the presence of higherantibodies levels of VZV in the CSF than in the serum orby a positive VZV PCR in the CSF [26].Copyright © Lippincott Williams & Wilkins. Unauthorized reproduction of this article is prohibited.
Page 1: Central nervous system vasculitisRu
Page 5 and 6: 14 Vasculitis syndromes[41 ]. Othe
Page 8 and 9: Central nervous system vasculitis H

Central nervous system vasculitis

You also want an ePaper? Increase the reach of your titles

Delete template?

Save as template?