Brzosko M, Fiedorowicz-Fabrycy I, Honczarenko K
Klinicznego Oddziału Reumatologii Instytutu Chorób Wewetrznych PAM w Szczecinie.
Neurol Neurochir Pol. 1996 May-Jun;30(3):475-80.
A case of 33-year-old man, who underwent numerous hospital admissions caused by multiple progressing disseminated neurological abnormalities is presented. At first multiple sclerosis was a tentative diagnosis. Because of persistent eosinophilia, after exclusion of other causes of increased eosinophil count, idiopathic hyperoesinophilic syndrome was diagnosed. The case was confirmed neuropathologically. The authors discuss causes of idiopathic hyperoesinophilic syndrome. Very exceptional history of the syndrome, with dominant CNS involvement, is discussed.
本文报告一例33岁男性患者，因多发性进行性播散性神经功能异常多次入院。最初初步诊断为多发性硬化症。由于持续性嗜酸性粒细胞增多，在排除嗜酸性粒细胞计数增加的其他原因后，诊断为特发性高嗜酸性粒细胞综合征。该病例经神经病理学证实。作者讨论了特发性高嗜酸性粒细胞综合征的病因。并讨论了该综合征非常罕见的病史，以中枢神经系统受累为主。
