神经髓鞘病--对印度南部一家三级医疗中心十三例病例的回顾性研究。

IF 1.4 4区医学 Q4 IMMUNOLOGY Indian Journal of Medical Microbiology Pub Date : 2024-11-01 DOI:10.1016/j.ijmmb.2024.100751

G. Vithiya , Preethi G. Rajalakshmi , P Shunmuga Sundaram , T. Rajendran

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引用次数: 0

摘要

鉴于其罕见性和致命后果，神经性美拉德氏病值得关注。我们对 2017 年至 2023 年间报告的经培养确诊的神经性美拉德氏病进行了回顾性研究。共发现 13 名患者，中位年龄为 43 岁，除 3 名男性外，其余均为男性。57%的病例（7/13）脑实质受累，表现为脑炎、脑炎、大脓肿或小脓肿。三名患者患有脊髓炎和脊髓小脓肿，另有三名患者患有脑静脉血栓。五名患者在住院期间死亡。两名患者因经济拮据，不听医嘱出院。六名幸存者接受了一至八个月的随访。

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Neuromelioidosis – A retrospective review of thirteen cases from a tertiary care centre from South India

Neurologic melioidosis warrants attention in view of its rarity and lethal consequences. We performed a retrospective review of culture confirmed neurologic melioidosis reported between 2017 and 2023. Thirteen patients were identified with median age 43 years and all but three were males. Brain parenchyma was involved in 57 % cases (7/13) as cerebritis, encephalitis and macro abscess or micro abscess. Three patients had myelitis with spinal cord micro abscess and cerebral venous thrombosis in three other patients. Five patients died during hospitalization. Two were discharged against medical advice due to financial constraints. Six survivors were followed between one and eight months.

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来源期刊

Indian Journal of Medical Microbiology IMMUNOLOGY-

CiteScore

2.20

自引率

0.00%

发文量

154

审稿时长

73 days

期刊介绍： Manuscripts of high standard in the form of original research, multicentric studies, meta analysis, are accepted. Current reports can be submitted as brief communications. Case reports must include review of current literature, clinical details, outcome and follow up. Letters to the editor must be a comment on or pertain to a manuscript already published in the IJMM or in relation to preliminary communication of a larger study. Review articles, Special Articles or Guest Editorials are accepted on invitation.