Skip to main content
Top
Published in: BMC Neurology 1/2020

Open Access 01-12-2020 | Magnetic Resonance Imaging | Case report

Acute progressive stroke with middle cerebral artery occlusion caused by idiopathic hypereosinophilic syndrome: a case report

Authors: Quan-Fu Li, Qing Zhang, Yue-Fang Huang, Zheng-Xiang Zhang

Published in: BMC Neurology | Issue 1/2020

Login to get access

Abstract

Background

Idiopathic hypereosinophilic syndrome (IHES) is associated with various organ system dysfunctions. Neurologic abnormalities have been previously noted in this syndrome. Cerebral infarction secondary to occlusion of large cerebral artery is rarely reported. Here we described a patient with IHES presented progressive multiple cerebral infarctions caused by bilateral middle cerebral artery occlusion.

Case presentation

A 55-year-old Chinese woman presented to our hospital with acute onset of right limbs weakness and slurred speech. Laboratory tests showed a significant eosinophilia of 5.29 × 109/L (normal, < 0.5), 49.9% of leukocytes. Brain magnetic resonance imaging (MRI) revealed multiple acute cerebral ischemic lesions. Magnetic resonance angiography (MRA) demonstrated stenosis in horizontal segment of right middle cerebral artery. A pretibial skin biopsy revealed eosinophilic infiltration around the capillaries in deep dermis and adipose tissue. The patient was given oral dual anti platelet agents and intravenous methylprednisolone. However, one week later, the patient presented significant neurological deterioration with right-sided hemiparesis and totally motor aphasia. Brain MRI and computed tomography perfusion (CTP) demonstrated new acute cerebral ischemia in left hemisphere. Digital subtraction angiography (DSA) revealed left middle cerebral artery completely occluded. The patient received a high-dose of intravenous methylprednisolone 500 mg per day and the eosinophil count quickly fell to normal within 2 days. She was transferred to a rehabilitation center and her neurological symptoms improved with modified Ranking Scale from 4 to 2.

Conclusions

IHES is one of the rare causes of acute ischemic stroke with large cerebral artery occlusion. An early high-dose of corticosteroids therapy should be considered in cases of IHES patients. Our case study is benefit to clinical diagnosis and treatment of cerebral infarction with IHES.
Literature
1.
go back to reference Simon HU, Rothenberg ME, Bochner BS, Weller PF, Wardlaw AJ, Wechsler ME, et al. Refining the definition of hypereosinophilic syndrome. J Allergy Clin Immunol. 2010;126(1):45–9.CrossRef Simon HU, Rothenberg ME, Bochner BS, Weller PF, Wardlaw AJ, Wechsler ME, et al. Refining the definition of hypereosinophilic syndrome. J Allergy Clin Immunol. 2010;126(1):45–9.CrossRef
2.
go back to reference Curtis C, Ogbogu P. Hypereosinophilic syndrome. Clin Rev Allergy Immunol. 2016;50(2):240–51.CrossRef Curtis C, Ogbogu P. Hypereosinophilic syndrome. Clin Rev Allergy Immunol. 2016;50(2):240–51.CrossRef
3.
go back to reference Psychogios K, Evmorfiadis I, Dragomanovits S, Stavridis A, Takis K, Kaklamanis L, et al. ANCA-negative Churg-Strauss syndrome presenting as acute multiple cerebral infarcts: a case report. J Stroke Cerebrovasc Dis. 2017;26(3):e47–9.CrossRef Psychogios K, Evmorfiadis I, Dragomanovits S, Stavridis A, Takis K, Kaklamanis L, et al. ANCA-negative Churg-Strauss syndrome presenting as acute multiple cerebral infarcts: a case report. J Stroke Cerebrovasc Dis. 2017;26(3):e47–9.CrossRef
4.
go back to reference Chen H, Raza HK, Jing J, Shen D, Xu P, Zhou S, et al. Hypereosinophilic syndrome with central nervous system involvement: two case reports and literature review. Brain Inj. 2017;31(12):1695–700.CrossRef Chen H, Raza HK, Jing J, Shen D, Xu P, Zhou S, et al. Hypereosinophilic syndrome with central nervous system involvement: two case reports and literature review. Brain Inj. 2017;31(12):1695–700.CrossRef
5.
go back to reference Montgomery ND, Dunphy CH, Mooberry M, Laramore A, Foster MC, Park SI, et al. Diagnostic complexities of eosinophilia. Arch Pathol Lab Med. 2013;137(2):259–69.CrossRef Montgomery ND, Dunphy CH, Mooberry M, Laramore A, Foster MC, Park SI, et al. Diagnostic complexities of eosinophilia. Arch Pathol Lab Med. 2013;137(2):259–69.CrossRef
6.
go back to reference Moore PM, Harley JB, Fauci AS. Neurologic dysfunction in the idiopathic hypereosinophilic syndrome. Ann Intern Med. 1985;102(1):109–14.CrossRef Moore PM, Harley JB, Fauci AS. Neurologic dysfunction in the idiopathic hypereosinophilic syndrome. Ann Intern Med. 1985;102(1):109–14.CrossRef
7.
go back to reference Wise FM, Olver JH. A 66-year-old man with multiple cerebral and cerebellar infarcts due to idiopathic hypereosinophilic syndrome. J Clin Neurosci. 2013;20(10):1442–3.CrossRef Wise FM, Olver JH. A 66-year-old man with multiple cerebral and cerebellar infarcts due to idiopathic hypereosinophilic syndrome. J Clin Neurosci. 2013;20(10):1442–3.CrossRef
8.
go back to reference Wu X, Guo Y, Tan X. Acute cerebral infarction in watershed distribution in a patient with hypereosinophilic syndrome without cardiac lesion. Neurol Sci. 2014;35(10):1607–10.CrossRef Wu X, Guo Y, Tan X. Acute cerebral infarction in watershed distribution in a patient with hypereosinophilic syndrome without cardiac lesion. Neurol Sci. 2014;35(10):1607–10.CrossRef
9.
go back to reference Bolz J, Meves SH, Kara K, Reinacher-Schick A, Gold R, Krogias C. Multiple cerebral infarctions in a young patient with heroin-induced hypereosinophilic syndrome. J Neurol Sci. 2015;356(1–2):193–5.CrossRef Bolz J, Meves SH, Kara K, Reinacher-Schick A, Gold R, Krogias C. Multiple cerebral infarctions in a young patient with heroin-induced hypereosinophilic syndrome. J Neurol Sci. 2015;356(1–2):193–5.CrossRef
10.
go back to reference Takeuchi S, Takasato Y, Masaoka H, Hayakawa T, Otani N, Yoshino Y, et al. Middle cerebral artery occlusion resulting from hypereosinophilic syndrome. J Clin Neurosci. 2010;17(3):377–8.CrossRef Takeuchi S, Takasato Y, Masaoka H, Hayakawa T, Otani N, Yoshino Y, et al. Middle cerebral artery occlusion resulting from hypereosinophilic syndrome. J Clin Neurosci. 2010;17(3):377–8.CrossRef
11.
go back to reference Raut TP, Baheti G, Raut S, Bhattad D, Jain P, Jain A. A tale of recurrent strokes due to Hypereosinophilic syndrome. Med Clin Rev. 2017;3(3):16. Raut TP, Baheti G, Raut S, Bhattad D, Jain P, Jain A. A tale of recurrent strokes due to Hypereosinophilic syndrome. Med Clin Rev. 2017;3(3):16.
12.
go back to reference Sethi HS, Schmidley JW. Cerebral infarcts in the setting of eosinophilia: three cases and a discussion. Arch Neurol. 2010;67(10):1275–7.CrossRef Sethi HS, Schmidley JW. Cerebral infarcts in the setting of eosinophilia: three cases and a discussion. Arch Neurol. 2010;67(10):1275–7.CrossRef
13.
go back to reference Chang WL, Lin HJ, Cheng HH. Hypereosinophilic syndrome with recurrent strokes: A case report. Acta Neurol Taiwan. 2008;17(3):184–8. Chang WL, Lin HJ, Cheng HH. Hypereosinophilic syndrome with recurrent strokes: A case report. Acta Neurol Taiwan. 2008;17(3):184–8.
14.
go back to reference Ogbogu PU, Bochner BS, Butterfield JH, Gleich GJ, Huss-Marp J, Kahn JE, et al. Hypereosinophilic syndrome: a multicenter, retrospective analysis of clinical characteristics and response to therapy. J Allergy Clin Immunol. 2009;124(6):1319–25. Ogbogu PU, Bochner BS, Butterfield JH, Gleich GJ, Huss-Marp J, Kahn JE, et al. Hypereosinophilic syndrome: a multicenter, retrospective analysis of clinical characteristics and response to therapy. J Allergy Clin Immunol. 2009;124(6):1319–25.
Metadata
Title
Acute progressive stroke with middle cerebral artery occlusion caused by idiopathic hypereosinophilic syndrome: a case report
Authors
Quan-Fu Li
Qing Zhang
Yue-Fang Huang
Zheng-Xiang Zhang
Publication date
01-12-2020
Publisher
BioMed Central
Published in
BMC Neurology / Issue 1/2020
Electronic ISSN: 1471-2377
DOI
https://doi.org/10.1186/s12883-020-01941-8

Other articles of this Issue 1/2020

BMC Neurology 1/2020 Go to the issue