Literature DB >> 10209533

[Recurrent subacute encephalopathy in the framework of idiopathic hypereosinophilic syndrome].

B Balestra1, P Pedrazzi, F Regli.   

Abstract

HISTORY: An 81-year-old man, previously good health, suddenly developed confusion and rapidly progressive severe tetraparesis. INVESTIGATIONS: Peripheral blood and bone marrow revealed marked eosinophilia: allergic, parasitic, neoplastic or vasculitic causes were excluded. Magnetic resonance imaging demonstrated multiple lesions in the cortical and subcortical white matter. DIAGNOSIS, TREATMENT AND COURSE: The findings indicated idiopathic hypereosinophilic syndrome involving the central nervous system and treatment with high doses of glucocorticoids was started. After a stormy course almost complete recovery occurred.
CONCLUSION: Idiopathic hypereosinophilic syndrome can rarely manifest itself a an isolated severe subacute encephalopathy.

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Year:  1999        PMID: 10209533     DOI: 10.1055/s-2007-1024301

Source DB:  PubMed          Journal:  Dtsch Med Wochenschr        ISSN: 0012-0472            Impact factor:   0.628


  1 in total

1.  Association of the blood eosinophil count with end-organ symptoms.

Authors:  Ole Weis Bjerrum; Volkert Siersma; Hans Carl Hasselbalch; Bent Lind; Christen Lykkegaard Andersen
Journal:  Ann Med Surg (Lond)       Date:  2019-07-09
  1 in total

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