J Clin Neurol.  2011 Mar;7(1):40-42. 10.3988/jcn.2011.7.1.40.

Multiple Cerebral Arterial Stenosis Associated with Hepatitis B Virus Infection

Affiliations
  • 1Department of Neurology, Cerebrovascular Center, Chonnam National University Hospital, Gwangju, Korea. mspark@jnu.ac.kr
  • 2Department of Neurology, Chonnam National University Hwasun Hospital, Hwasun, Korea.

Abstract

BACKGROUND
There are conflicting findings regarding the association between hepatitis B (HB) virus (HBV) infection and atherosclerosis.
CASE REPORT
A 34-year-old man was admitted for transient dysarthria and facial palsy. Ten years previously he had been diagnosed with HBV infection and treated with lamivudine (100 mg/day). Reactivation of HBV was detected 6 months before this recent admission. Serologic tests revealed that he was positive for HB early antigen, HB surface antigen, and anti-HB core. Brain magnetic resonance images were normal, but magnetic resonance angiograms revealed severe stenosis of the right middle cerebral artery, both external carotid arteries, and the basilar artery.
CONCLUSIONS
This case report reveals that a young patient with reactivated HBV developed multiple arterial stenoses even though he had no risk factors for this disease.

Keyword

hepatitis B virus; atherosclerosis; reactivated HBV infection; multiple cerebral arterial stenoses

MeSH Terms

Adult
Antigens, Surface
Atherosclerosis
Brain
Carotid Artery, External
Constriction, Pathologic
Dysarthria
Facial Paralysis
Hepatitis
Hepatitis B
Hepatitis B virus
Humans
Lamivudine
Magnetic Resonance Spectroscopy
Middle Cerebral Artery
Risk Factors
Serologic Tests
Viruses
Antigens, Surface
Lamivudine

Figure

  • Fig. 1 Conventional cerebral angiogram. A: Right carotid angiogram showing severe focal stenosis in the midportion of the middle cerebral artery (arrows) that is eccentric and irregular. B: Carotid angiogram showing stenosis of both external carotid arteries (dotted arrows). C: Right vertebral arteriogram showing severe stenosis of the proximal basilar artery and left distal vertebral artery (arrows).


Reference

1. Epstein SE, Zhou YF, Zhu J. Infection and atherosclerosis: emerging mechanistic paradigms. Circulation. 1999. 100:e20–e28.
2. Fattovich G, Brollo L, Giustina G, Noventa F, Pontisso P, Alberti A, et al. Natural history and prognostic factors for chronic hepatitis type B. Gut. 1991. 32:294–298.
Article
3. Wanless IR, Wong F, Blendis LM, Greig P, Heathcote EJ, Levy G. Hepatic and portal vein thrombosis in cirrhosis: possible role in development of parenchymal extinction and portal hypertension. Hepatology. 1995. 21:1238–1247.
Article
4. Friedman SL. Seminars in medicine of the Beth Israel Hospital, Boston. The cellular basis of hepatic fibrosis. Mechanisms and treatment strategies. N Engl J Med. 1993. 328:1828–1835.
Article
5. Ishizaka N, Ishizaka Y, Takahashi E, Toda Ei E, Hashimoto H, Ohno M, et al. Increased prevalence of carotid atherosclerosis in hepatitis B virus carriers. Circulation. 2002. 105:1028–1030.
Article
6. Sung J, Song YM, Choi YH, Ebrahim S, Davey Smith G. Hepatitis B virus seropositivity and the risk of stroke and myocardial infarction. Stroke. 2007. 38:1436–1441.
Article
7. Swartz RH, Bhuta SS, Farb RI, Agid R, Willinsky RA, Terbrugge KG, et al. Intracranial arterial wall imaging using high-resolution 3-tesla contrast-enhanced MRI. Neurology. 2009. 72:627–634.
Article
8. Mason A, Wick M, White H, Perrillo R. Hepatitis B virus replication in diverse cell types during chronic hepatitis B virus infection. Hepatology. 1993. 18:781–789.
Article
9. Deeren DH, De Backer AI, Malbrain ML, Verbraeken H, Blockmans D. Treatment of hepatitis B virus-related polyarteritis nodosa: two case reports and a review of the literature. Clin Rheumatol. 2004. 23:172–176.
Article
10. Trepo C, Guillevin L. Polyarteritis nodosa and extrahepatic manifestations of HBV infection: the case against autoimmune intervention in pathogenesis. J Autoimmun. 2001. 16:269–274.
Article
11. Baig S, Alamgir M. The extrahepatic manifestations of hepatitis B virus. J Coll Physicians Surg Pak. 2008. 18:451–457.
12. Muhlestein JB. Chronic infection and coronary artery disease. Med Clin North Am. 2000. 84:123–148.
Article
13. Saikku P, Leinonen M, Mattila K, Ekman MR, Nieminen MS, Mäkelä PH, et al. Serological evidence of an association of a novel Chlamydia, TWAR, with chronic coronary heart disease and acute myocardial infarction. Lancet. 1988. 2:983–986.
Article
14. Kiechl S, Egger G, Mayr M, Wiedermann CJ, Bonora E, Oberhollenzer F, et al. Chronic infections and the risk of carotid atherosclerosis: prospective results from a large population study. Circulation. 2001. 103:1064–1070.
Article
15. Ludewig B, Freigang S, Jäggi M, Kurrer MO, Pei YC, Vlk L, et al. Linking immune-mediated arterial inflammation and cholesterol-induced atherosclerosis in a transgenic mouse model. Proc Natl Acad Sci U S A. 2000. 97:12752–12757.
Article
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