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由奴卡菌引起的特发性血小板减少性紫癜合并脑脓肿的诊断:采用脑脊液宏基因组下一代测序技术的病例报告。

Idiopathic thrombocytopenic purpura with brain abscess caused by Nocardia farcinica diagnosed using metagenomics next-generation sequencing of the cerebrospinal fluid: a case report.

机构信息

Department of Neurology, The First People's Hospital of Changde City, Changde, Hunan, China.

出版信息

BMC Infect Dis. 2021 Apr 23;21(1):380. doi: 10.1186/s12879-021-06071-1.

Abstract

BACKGROUND

Brain abscesses caused by Nocardia farcinica are rare, and mostly occur in immunocompromised individuals. Rapid and accurate diagnosis of nocardiosis is challenging. Due to the inadequate performance of conventional diagnostic methods for Nocardia infection, metagenomics next-generation sequencing (mNGS) of cerebrospinal fluid (CSF) has the potential to improve the diagnosis intracranial nocardiosis.

CASE PRESENTATION

We report a case of 50-year-old man with brain abscess caused by Nocardia farcinica. The patient had a idiopathic thrombocytopenic purpura complication that required long-term methylprednisolone administration. His chest image showed multiple lesions, which had been misdiagnosed as lung cancer, and his head image showed multiple intracranial metastases. No pathogen was detected in routine examinations including blood culture, sputum culture and traditional culture methods of cerebrospinal fluid. In order to accurately identify the pathogen, mNGS was used to detect Nocardia in CSF. Although the patient's condition improved after using sensitive antibiotics, he transferred to the local hospital for treatment because of many complicated diseases and family financial limitations.

CONCLUSION

This case highlights the value of mNGS in the diagnosis of Nocardia brain abscess, and emphasizes the inadequate sensitivity of conventional diagnostic methods for Nocardia infection. Using mNGS can facilitate early and accurate detection of Norcadia-associated of meningitis in immunocompromised patients, thereby reducing unnecessary use of antibiotics and reducing mortality of the disease.

摘要

背景

由星形诺卡菌引起的脑脓肿较为罕见,且多发生于免疫功能低下的个体。快速、准确地诊断诺卡菌病具有挑战性。由于传统的诺卡菌感染诊断方法的性能不足,脑脊液的宏基因组下一代测序(mNGS)有可能提高颅内诺卡菌病的诊断能力。

病例介绍

我们报告了一例由星形诺卡菌引起的 50 岁男性脑脓肿病例。该患者患有特发性血小板减少性紫癜,需要长期服用甲基强的松龙。他的胸部影像显示多个病变,曾误诊为肺癌,头部影像显示多个颅内转移。常规检查包括血培养、痰培养和传统的脑脊液培养方法均未检测到病原体。为了准确识别病原体,我们使用 mNGS 检测了脑脊液中的诺卡菌。尽管患者在使用敏感抗生素后病情有所改善,但由于多种复杂疾病和家庭经济限制,他转至当地医院治疗。

结论

本病例突出了 mNGS 在星形诺卡菌脑脓肿诊断中的价值,并强调了传统的诺卡菌感染诊断方法的敏感性不足。使用 mNGS 可以促进免疫功能低下患者中与诺卡菌相关脑膜炎的早期、准确检测,从而减少不必要的抗生素使用,并降低疾病的死亡率。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/657c/8066483/51ef1856c692/12879_2021_6071_Fig1_HTML.jpg

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