Dbaibou Jana, Levine Diane L
Internal Medicine, Wayne State University, Detroit Medical Center, Detroit, USA.
Cureus. 2020 Apr 20;12(4):e7748. doi: 10.7759/cureus.7748.
Cryptococcosis is an opportunistic fungal infection found in both immunocompromised and non-immunocompromised patients; however, it is particularly prevalent in those with Human Immunodeficiency Virus/Acquired Immunodeficiency Syndrome (HIV/AIDS). Patients with isolated pulmonary cryptococcosis can present with heterogeneous symptoms. The rarity of this entity makes it difficult to recognize and diagnose. We present a case of a 54-year-old female with poorly controlled HIV and seizure disorder, who presented with suspected seizures. Her CD4 count was 7. Due to fever and headache, cryptococcal meningitis was suspected, and she was empirically started on liposomal amphotericin and flucytosine. Computed tomography (CT) of the head was negative for any acute intracranial process. Serum cryptococcal antigen was positive; however cerebrospinal fluid (CSF) studies from lumbar puncture (LP) were entirely negative, including CSF cryptococcal antigen. CT thorax demonstrated interval development of two solid pulmonary nodules in the right upper lobe (RUL). There was no other evidence of disseminated cryptococcal disease. CT-guided biopsy of the larger RUL was compatible with Cryptococcus species. Fungal cultures of sputum and blood were negative. The patient improved, and therapy was de-escalated from liposomal amphotericin and flucytosine to oral fluconazole, with a plan to complete a six- to twelve-month course of therapy. This case illustrates that in rare cases, Cryptococcal disease may still be localized despite having a positive serum Cryptococcal antigen. It also emphasizes the importance of a thorough investigation with multimodal diagnostic tools to evaluate for disseminated Cryptococcal disease, especially in those with a history of immunocompromise.
隐球菌病是一种在免疫功能低下和免疫功能正常的患者中均可发现的机会性真菌感染;然而,它在人类免疫缺陷病毒/获得性免疫缺陷综合征(HIV/AIDS)患者中尤为常见。孤立性肺隐球菌病患者的症状可能多种多样。这种疾病的罕见性使其难以识别和诊断。我们报告一例54岁女性病例,该患者HIV控制不佳且患有癫痫障碍,因疑似癫痫发作前来就诊。她的CD4细胞计数为7。由于发热和头痛,怀疑患有隐球菌性脑膜炎,遂经验性地开始使用脂质体两性霉素和氟胞嘧啶治疗。头部计算机断层扫描(CT)未发现任何急性颅内病变。血清隐球菌抗原呈阳性;然而,腰椎穿刺(LP)获得的脑脊液(CSF)检查结果完全为阴性,包括脑脊液隐球菌抗原。胸部CT显示右上叶(RUL)出现两个实性肺结节。没有其他播散性隐球菌病的证据。对较大的右上叶结节进行CT引导下活检,结果与隐球菌属相符。痰液和血液的真菌培养均为阴性。患者病情好转,治疗方案从脂质体两性霉素和氟胞嘧啶降级为口服氟康唑,并计划完成6至12个月的疗程。该病例表明,在罕见情况下,尽管血清隐球菌抗原呈阳性,但隐球菌病仍可能局限。它还强调了使用多模式诊断工具进行全面调查以评估播散性隐球菌病的重要性,尤其是在有免疫功能低下病史的患者中。