Departments of1Neurosurgery.
2Neuropathology.
Neurosurg Focus. 2019 Aug 1;47(2):E14. doi: 10.3171/2019.5.FOCUS19252.
Intracranial fungal granuloma (IFG) remains an uncommon entity. The authors report a single-institute study of 90 cases of IFG, which is the largest study until now.
In this retrospective study, all cases of IFG surgically treated in the years 2001-2018 were included. Data were obtained from the medical records and the pathology, microbiology, and radiology departments. All relevant clinical data, imaging characteristics, surgical procedure performed, perioperative findings, and follow-up data were recorded from the case files. Telephonic follow-up was also performed for a few patients to find out their current status.
A total of 90 cases consisting of 64 males (71.1%) and 26 (28.9%) females were evaluated. The mean patient age was 40.2 years (range 1-79 years). Headache (54 patients) was the most common presenting complaint, followed by visual symptoms (35 patients), fever (21 patients), and others such as limb weakness (13 patients) or seizure (9 patients). Cranial nerve involvement was the most common sign (47 patients), followed by motor deficit (22 patients) and papilledema (7 patients). The mean duration of symptoms before presentation was 6.4 months (range 0.06-48 months). Thirty patients (33.3%) had predisposing factors like diabetes mellitus, tuberculosis, or other immunocompromised status. A pure intracranial location of the IFG was seen in 49 cases (54.4%), whereas rhinocerebral or paranasal sinus involvement was seen in 41 cases (45.6%). Open surgery, that is, craniotomy and decompression, was performed in 55 cases, endoscopic biopsy was done in 30 cases, and stereotactic biopsy was performed in 5 cases. Aspergilloma (43 patients) was the most common fungal mass, followed by zygomycosis (13 patients), chromomycosis (9 patients), cryptococcoma (7 patients), mucormycosis (5 patients), and candida infection (1 patient). In 12 cases, the exact fungal phenotype could not be identified. Follow-up was available for 69/90 patients (76.7%). The mean duration of the follow-up was 37.97 months (range 3-144 months). The mortality rate was 52.2% (36/69 patients) among the patients with available follow-up.
A high index of suspicion for IFG should exist for patients with an immunocompromised status and diabetic patients with rhinocerebral mass lesions. Early diagnosis, aggressive surgical decompression, and a course of promptly initiated antifungal therapy are associated with a better prognosis.
颅内真菌性肉芽肿(IFG)仍然是一种罕见的疾病。作者报告了一项关于 90 例 IFG 的单中心研究,这是迄今为止最大的研究。
在这项回顾性研究中,纳入了 2001 年至 2018 年期间接受 IFG 手术治疗的所有病例。数据来自病历、病理学、微生物学和放射学部门。从病例档案中记录所有相关的临床数据、影像学特征、手术过程、围手术期发现和随访数据。还对一些患者进行了电话随访,以了解他们的现状。
共评估了 90 例病例,其中 64 例为男性(71.1%),26 例为女性(28.9%)。患者的平均年龄为 40.2 岁(范围 1-79 岁)。头痛(54 例)是最常见的首发症状,其次是视觉症状(35 例)、发热(21 例)和其他症状,如肢体无力(13 例)或癫痫发作(9 例)。颅神经受累是最常见的体征(47 例),其次是运动障碍(22 例)和视乳头水肿(7 例)。从出现症状到就诊的平均时间为 6.4 个月(范围 0.06-48 个月)。30 例(33.3%)患者存在糖尿病、结核病或其他免疫抑制状态等易患因素。49 例(54.4%)为单纯颅内 IFG ,41 例(45.6%)为鼻颅或副鼻窦受累。55 例行开颅手术,即开颅减压,30 例行内镜活检,5 例行立体定向活检。曲霉菌瘤(43 例)是最常见的真菌肿块,其次是毛霉菌病(13 例)、着色真菌病(9 例)、隐球菌病(7 例)、坏死性真菌病(5 例)和念珠菌感染(1 例)。在 12 例中,无法明确确定确切的真菌表型。69/90 例(76.7%)患者有随访资料。随访的平均时间为 37.97 个月(范围 3-144 个月)。在有随访资料的患者中,死亡率为 52.2%(36/69 例)。
对于免疫功能低下和糖尿病合并鼻颅肿块的患者,应高度怀疑 IFG。早期诊断、积极的手术减压和及时启动抗真菌治疗与更好的预后相关。