Literature DB >> 21628939

Fatal encephalitis in a case of hypereosinophilic syndrome: MRI and autopsy findings.

Zen Kobayashi1, Kuniaki Tsuchiya, Hiroshi Komachi, Kazunori Miki, Osamu Yokota, Tetsuaki Arai, Hirotomo Miake, Hideki Ishizu, Haruhiko Akiyama, Hidehiro Mizusawa.   

Abstract

A 34-year-old man developed fever and headache, followed by finger tremor and gait disturbance, and was admitted to our hospital about two months after onset. Blood tests showed a white blood cell count of 32,600 /µL with an eosinophil count of 22,300 /µL. There was no evidence of allergic drug reaction or parasitic infection. Cerebrospinal fluid examination demonstrated mononuclear pleocytosis without eosinophils or atypical cells. Brain MRI showed symmetric lesions bilaterally in the medial temporal lobe, frontobasal and insular regions and medulla oblongata. Herpes simplex virus-DNA was negative in the cerebrospinal fluid. The patient died about four months after onset. Histopathologically, there was infiltration of T cells, B cells and macrophages throughout the whole brain, but eosinophils or atypical cells were absent. Immunohistochemistry for herpes simplex virus type 1 and human herpesvirus 6 was negative. This case suggests that fatal encephalitis may develop in association with hypereosinophilic syndrome.

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Year:  2011        PMID: 21628939     DOI: 10.2169/internalmedicine.50.4570

Source DB:  PubMed          Journal:  Intern Med        ISSN: 0918-2918            Impact factor:   1.271


  1 in total

1.  Idiopathic hypereosinophilic syndrome: a new cause of vasculitis of the central nervous system.

Authors:  C M Rice; K M Kurian; S Renowden; A Whiteway; C Price; N J Scolding
Journal:  J Neurol       Date:  2015-04-07       Impact factor: 4.849

  1 in total

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