[Neurocryptococcosis waiting to be diagnosed].

Ahmed Ashrin, Suzanne Tran, Ariane Gavaud, Marine Armand, Lauriane Geoffray, Magali Le Garff-Tavernier, David Saadoun, Cécile Nabet, Elise Sourdeau
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引用次数: 0

Abstract

Neurocryptococcosis is a severe neurological complication of Cryptococcus neoformans infections, primarily affecting immunocompromised individuals. This report describes the case of a 53-year-old man with no known medical history who experienced severe headaches and vomiting while on a business trip to Pakistan. He was given preventive antibiotic therapy, followed by a combination of sulfamethoxazole and trimethoprim for suspected toxoplasmosis. The patient's condition initially improved and he was discharged from the hospital, but later experienced a recurrence of symptoms and sought emergency care. The diagnosis of neurocryptococcosis was confirmed through various biological tests, including flow cytometry. Treatment with Amphotericin B and 5-Fluorocytosine was initiated. Further testing revealed significant CD4+ T-cell lymphopenia, which was attributed to sarcoidosis-like systemic granulomatosis. This case presents an atypical clinical manifestation, with the abrupt onset of an opportunistic infection in a patient without any known immunosuppression.

[等待诊断的神经隐球菌病]。
神经隐球菌病是新生隐球菌感染引起的严重神经系统并发症,主要影响免疫力低下的人群。本报告描述了一名 53 岁男性的病例,他没有已知病史,在巴基斯坦出差期间出现严重头痛和呕吐。他接受了预防性抗生素治疗,随后又接受了磺胺甲噁唑和三甲氧苄氨嘧啶的联合治疗,以治疗疑似弓形虫病。患者的病情起初有所好转并出院,但后来症状复发,于是寻求急诊治疗。通过流式细胞术等各种生物检测,确诊为神经隐球菌病。他开始接受两性霉素 B 和 5-氟胞嘧啶治疗。进一步检测发现,患者出现了明显的 CD4+ T 细胞淋巴细胞减少症,这被归因于肉样瘤样全身肉芽肿病。该病例临床表现不典型,患者在没有任何已知免疫抑制的情况下突然出现机会性感染。
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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