Grant G A, Kim D K, Shaw C M, Berger M S
Department of Neurological Surgery, University of Washington School of Medicine, Seattle, USA.
Brain Tumor Pathol. 1999;16(1):55-9. doi: 10.1007/BF02478903.
A solitary eosinophilic granuloma of the central nervous system is an unusual manifestation of histiocytosis X. A unique case of a solitary eosinophilic granuloma of the right temporal lobe without osseous involvement is described. A 20-year-old man presented with a grand mal seizure. Magnetic resonance imaging demonstrated an intraaxial enhancing mass in the right temporal lobe with marked vasogenic edema. A right temporal craniotomy was performed for resection of the lesion and the diagnosis of an eosinophilic granuloma was confirmed by histopathology. Follow-up MR imaging obtained 5 years following resection demonstrated no recurrence. Solitary eosinophilic granuloma should be considered in the differential diagnosis of enhancing mass lesions affecting the central nervous system. Although the natural history of solitary eosinophilic granulomas remains poorly defined, surgical treatment still remains the mainstay of therapy for these unifocal cerebral lesions.
中枢神经系统孤立性嗜酸性肉芽肿是组织细胞增多症X的一种不寻常表现。本文描述了一例独特的右侧颞叶孤立性嗜酸性肉芽肿,无骨质受累。一名20岁男性出现大发作。磁共振成像显示右侧颞叶轴内强化肿块,伴有明显的血管源性水肿。行右侧颞叶开颅术切除病变,组织病理学证实为嗜酸性肉芽肿。切除术后5年的随访磁共振成像显示无复发。在鉴别影响中枢神经系统的强化肿块病变时,应考虑孤立性嗜酸性肉芽肿。尽管孤立性嗜酸性肉芽肿的自然病程仍不明确,但手术治疗仍是这些单发性脑病变的主要治疗方法。