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小儿系统性红斑狼疮合并隐球菌性脑膜炎的非典型表现

Atypical Presentation of Pediatric Systemic Lupus Erythematosus Complicated by Cryptococcal Meningitis.

作者信息

Hashem Heba Ezzat, Ibrahim Zakaria Hamza

机构信息

Clinical Pathology Department, Ain Shams University, Cairo, Egypt.

General Surgery Department, Al-Azhar University, Cairo, Egypt.

出版信息

Case Rep Med. 2021 Feb 11;2021:6692767. doi: 10.1155/2021/6692767. eCollection 2021.

Abstract

BACKGROUND

is an opportunistic fungal pathogen that leads to life-threatening infections. Cryptococcal infections are mainly reported in HIV patients and less commonly encountered in non-HIV immunocompromised host. () is the most common species causing diseases in humans which can be presented as pulmonary, meningitis, cutaneous, and/or disseminated cryptococcosis. . A 12-year-old female girl from Cairo, Egypt, presented to the pediatric hospital with signs of systemic lupus erythematosus (SLE). She had an aggressive lupus nephritis course for which corticosteroids, mycophenolate mofetil, and cyclophosphamide were prescribed, and the child gradually improved and was discharged. Two months later, the patient exhibited skin lesions involved both in her legs, massive ulcers were developed and extended rapidly through the entire legs followed by deterioration in her conscious level, and signs of meningitis were documented. Cerebrospinal fluid (CSF) examination and microbiological workup were confirmatory for . infection, and mental and motor functions were rapidly deteriorated. Treatment with amphotericin B in addition to supportive treatment and close follow-up of the patient's medical condition result in obvious clinical improvement and patient discharge with minimal residual weakness in her legs after almost a one-month duration. After six months, the patient was brought to the emergency department complaining of repeated attacks of seizures, a lumbar puncture was performed, and culture results were again confirmatory for . . An intensive course of antifungal therapy was prescribed which was successful, evident by resolution of the signs and symptoms of infection in addition to negative culture results and negative sepsis biomarkers. The child clinically improved, but unfortunately, gradual optic nerve degeneration and brain cell atrophy as a sequel of severe and longstanding cryptococcal infection resulted in her death after almost one year from her first attack.

CONCLUSION

Cryptococcal infection among non-HIV patients is a rare disease but can result in advanced medical complications which may be fatal. The disease should be suspected to be reliably diagnosed. infection can be presented as a skin lesion which, if not treated properly at an earlier time, can result in dissemination and life-threatening consequences. Amphotericin B can be used effectively in cryptococcosis management in the settings where flucytosine is not available. Signs of cryptococcal meningitis can be manifested again after a period of remission and clinical cure which signifies the latency of in the central nervous system. The second activation of after its latency is usually life-threatening and mostly fatal.

摘要

背景

隐球菌是一种机会性真菌病原体,可导致危及生命的感染。隐球菌感染主要见于艾滋病患者,在非艾滋病免疫功能低下宿主中较少见。新型隐球菌是人类疾病最常见的致病菌种,可表现为肺隐球菌病、隐球菌性脑膜炎、皮肤隐球菌病和/或播散性隐球菌病。一名来自埃及开罗的12岁女童因系统性红斑狼疮(SLE)症状入住儿科医院。她患有侵袭性狼疮性肾炎,为此接受了皮质类固醇、霉酚酸酯和环磷酰胺治疗,患儿病情逐渐好转并出院。两个月后,患者双下肢出现皮肤病变,出现大量溃疡并迅速蔓延至整个下肢,随后意识水平下降,并有脑膜炎体征。脑脊液(CSF)检查和微生物学检查确诊为新型隐球菌感染,精神和运动功能迅速恶化。除支持治疗和密切监测患者病情外,使用两性霉素B治疗使患者临床症状明显改善,经过近一个月的治疗,患者出院时双下肢残留轻微无力。六个月后,患者因反复癫痫发作被送往急诊科,进行了腰椎穿刺,培养结果再次确诊为新型隐球菌感染。给予强化抗真菌治疗,治疗成功,感染的体征和症状消失,培养结果为阴性,败血症生物标志物也为阴性。患儿临床症状改善,但不幸的是,由于严重且长期的隐球菌感染导致视神经逐渐变性和脑细胞萎缩,患儿在首次发病后近一年死亡。

结论

非艾滋病患者的隐球菌感染是一种罕见疾病,但可导致严重的医学并发症,甚至可能致命。应怀疑该病以便可靠诊断。新型隐球菌感染可表现为皮肤病变,如果早期未得到适当治疗,可导致播散并产生危及生命的后果。在无法获得氟胞嘧啶的情况下,两性霉素B可有效用于隐球菌病的治疗。隐球菌性脑膜炎的体征在缓解期和临床治愈一段时间后可能再次出现,这表明新型隐球菌在中枢神经系统中具有潜伏性。新型隐球菌潜伏后的二次激活通常危及生命且大多致命。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eaee/7892246/0fd9a045c79d/CRIM2021-6692767.001.jpg

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