[Aspergillosis of the brain in a patient with pancytopenia].

Neuropatologia polska Pub Date : 1989-01-01
G M Szpakowa, E Tarnowska-Dziduszko, B Iwińska-Buksowicz
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Abstract

The here presented case concerns a 74-year-old woman treated for many years with steroids and immunosuppressive drugs during pancytopenia. Seven days before her death she developed severe headaches and visual disorders, rapidly increasing disturbances of consciousness and a temperature of 40 degrees C. The course of the disease was violent with meningeal syndrome and cerebral coma. The cerebrospinal fluid was purulent, pleocytosis 1235/ml, with prevalence of polymorphonuclear leucocytes (88%) and an protein level increased to 210 mg%. In autopsy no mycotic changes were found in the internal organs whereas in microscopic examination of the brain the dominant finding was the presence of numerous filamentous bodies with septa characteristic of aspergillus which were visible both in microthrombi in the lumen of meningeal and interstitial vessels and in the areas of extensive necroses in both cerebral hemispheres and the brain stem as well as within granulomas occurring on the edges of necrotic foci and in the inflammatory infiltration of the brain base meninges. The presence of aspergillus hyphae was usually associated with a severe inflammatory reaction of polymorphonuclear leucocytes, acidophilic and plasmatic cells in microabscesses and in the inflammatory infiltration of meninges or in the form of granulomas composed mainly of multinucleated giant cells of Langhans or of foreign body type and mononuclear cells. The etiopathogenesis of these changes is discussed. The role of the facilitating factor could have been played by protracted therapy with steroids and immunosuppressive drugs and/or by pancytopenia itself which is probably associated with abnormal immunological response. Noteworthy is the fact that the seldom described mycotic changes caused by aspergillus concerned in the present case the central nervous system exclusively.

[全血细胞减少症患者的脑曲霉病]。
本病例涉及一名74岁妇女,在全血细胞减少症期间接受类固醇和免疫抑制药物治疗多年。在她去世前7天,她出现了严重的头痛和视觉障碍,意识障碍迅速增加,体温达到40摄氏度。病程剧烈,伴有脑膜综合征和脑昏迷。脑脊液化脓,多胞1235/ml,多形核白细胞患病率(88%),蛋白水平升高至210 mg%。在尸检中,内脏没有发现真菌的变化,而在大脑的显微镜检查中,主要发现是存在许多丝状体,具有曲霉菌特征的间隔,在脑膜腔和间质血管的微血栓中,在大脑半球和脑干的广泛坏死区域,以及在坏死灶边缘和炎症处发生的肉芽肿中都可以看到脑膜的浸润。曲霉菌丝的存在通常与微脓肿中的多形核白细胞、嗜酸细胞和浆细胞的严重炎症反应以及脑膜的炎症浸润或主要由朗汉斯多核巨细胞或异物型和单核细胞组成的肉芽肿形式有关。讨论了这些变化的发病机制。促进因子的作用可能与类固醇和免疫抑制药物的长期治疗和/或全血细胞减少症本身有关,这可能与异常的免疫反应有关。值得注意的是,在本病例中,很少描述由曲霉引起的真菌性变化仅涉及中枢神经系统。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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