Cryptococcal Meningitis Beyond Immunosuppression: A Case Report in an Immunocompetent Individual.

IF 0.8 Q4 INFECTIOUS DISEASES
Case Reports in Infectious Diseases Pub Date : 2026-07-20 eCollection Date: 2026-01-01 DOI:10.1155/crdi/8630525
Ariba Sultan, Huda Raja, Amna Abrar, Abdullah Nadeem, Shameem Behram Khan, Nahid Raufi
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Abstract

Background: Cryptococcal meningitis is a life-threatening opportunistic fungal infection predominantly seen in immunocompromised hosts, yet it is increasingly recognized in apparently immunocompetent individuals. In tuberculosis-endemic regions, its diagnosis is frequently delayed or missed due to overlapping clinical and cerebrospinal fluid findings with tuberculous meningitis.

Case presentation: A 44-year-old immunocompetent woman presented with a two-month history of progressive diffuse headache and subjective bilateral lower limb weakness. Neurological examination was unremarkable, and initial cerebrospinal fluid analysis revealed marked hypoglycorrhachia (1 mg/dL), elevated protein (356 mg/dL), and lymphocytic pleocytosis. Brain imaging showed leptomeningeal enhancement without mass lesions. Despite negative microbiological testing for tuberculosis, empirical antituberculous therapy was initiated based on presumptive tuberculous meningitis. Pulmonary imaging demonstrated cavitary nodules and calcified lymph nodes. Lack of clinical improvement prompted further investigation; India ink staining and fungal culture of cerebrospinal fluid eventually confirmed Cryptococcus neoformans infection. The patient had no evidence of HIV, diabetes, or other immunosuppressive conditions. Induction therapy with liposomal amphotericin B and fluconazole was administered, followed by consolidation and maintenance fluconazole. She showed marked clinical and cerebrospinal fluid improvement and was discharged on oral fluconazole with sustained recovery.

Discussion: This case illustrates the diagnostic challenge of cryptococcal meningitis in immunocompetent patients, particularly in settings where tuberculous meningitis is common. Early reliance on India ink staining and fungal culture is essential when initial tuberculosis workup is negative or when response to antituberculous therapy is poor. The incidental detection of HHV-6 DNA likely represented viral reactivation without clinical significance.

Conclusion: Cryptococcal meningitis must be considered in immunocompetent patients presenting with chronic meningitis, even in the absence of classic risk factors. Prompt mycological investigation can prevent diagnostic delays and improve outcomes.

超越免疫抑制的隐球菌脑膜炎:一个免疫正常个体的病例报告。
背景:隐球菌性脑膜炎是一种危及生命的机会性真菌感染,主要见于免疫功能低下的宿主,但也越来越多地在明显免疫正常的个体中发现。在结核病流行地区,由于结核性脑膜炎的临床和脑脊液发现重叠,其诊断经常被延迟或遗漏。病例介绍:一名44岁免疫功能正常的女性,表现为两个月进行性弥漫性头痛和主观双侧下肢无力。神经学检查无明显异常,最初的脑脊液分析显示明显的低糖血症(1mg /dL)、蛋白升高(356 mg/dL)和淋巴细胞增多症。脑显像显示脑轻脑膜增强,无肿块病变。尽管结核病的微生物检测呈阴性,但根据推定结核性脑膜炎开始了经验性抗结核治疗。肺部影像学显示空洞结节和钙化淋巴结。缺乏临床改善促使进一步调查;墨迹染色及脑脊液真菌培养最终证实为新型隐球菌感染。患者没有HIV、糖尿病或其他免疫抑制疾病的证据。给予两性霉素B脂质体和氟康唑诱导治疗,随后氟康唑巩固和维持。她的临床和脑脊液有明显改善,出院时口服氟康唑,恢复持续。讨论:本病例说明了免疫功能正常患者隐球菌性脑膜炎的诊断挑战,特别是在结核性脑膜炎常见的环境中。当最初的结核病检查为阴性或抗结核治疗反应较差时,早期依赖印墨染色和真菌培养是必不可少的。偶然检测到HHV-6 DNA可能代表病毒再激活,没有临床意义。结论:即使在没有经典危险因素的情况下,免疫功能正常的慢性脑膜炎患者也必须考虑隐球菌性脑膜炎。及时的真菌学调查可以防止诊断延误并改善预后。
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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