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脑霉菌病:15个月内观察到的4例临床病理报告

Cerebral mycosis: clinico-pathological report of four cases observed in fifteen months.

作者信息

Bettoni L, Gabrielli M, Lechi A, Tedeschi F, Trabattoni G

出版信息

Ital J Neurol Sci. 1984 Dec;5(4):437-43. doi: 10.1007/BF02042629.

Abstract

Cerebral mycosis is a rare condition, difficult to diagnose in life, but is not easily missed at post-mortem examination. We report clinical and pathological findings in four patients with long duration prodromes, seizures and psychiatric symptoms. All of them had been misdiagnosed. Actinomycotic granules in two and Aspergillus filaments in the other patients were ascertained at histological examination. Two of the patients were in their twenties and apparently healthy. We suggest that the possibility of mycotic infection should be considered even in cases where no lowering of the body's defences can be postulated. Cell mediated immunity defects may be assumed as underlying these infections. Therefore we would suggest the importance of immunological tests for type IV immune responsiveness in all intracranial infective processes of undefined etiology.

摘要

脑霉菌病是一种罕见疾病,生前难以诊断,但尸检时不易漏诊。我们报告了4例有长期前驱症状、癫痫发作和精神症状患者的临床及病理表现。他们均被误诊。组织学检查确定其中2例有放线菌颗粒,另2例有曲霉菌丝。2例患者为20多岁,看似健康。我们建议,即使在无法推测机体防御功能降低的情况下,也应考虑霉菌感染的可能性。可认为细胞介导免疫缺陷是这些感染的潜在原因。因此,我们建议在所有病因不明的颅内感染过程中,进行IV型免疫反应性免疫学检测具有重要意义。

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