伴发噬血细胞性淋巴组织细胞增生症与吉兰-巴雷综合征：一例报告

-Associated Hemophagocytic Lymphohistiocytosis and Guillain-Barre Syndrome: A Case Report.

作者信息

Shi Fang-E, Chen Mei-Fang, Li Yong-Jie, Dong Gui-Ying, Zhu Ji-Hong

机构信息

Department of Emergency, Peking University People's Hospital, Beijing, China.

Department of Infectious Diseases, Peking University People's Hospital, Beijing, China.

出版信息

Front Med (Lausanne). 2022 Jul 7;9:895923. doi: 10.3389/fmed.2022.895923. eCollection 2022.

DOI:10.3389/fmed.2022.895923

PMID:35872780

原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9302883/

Abstract

(), a Gram-negative bacterium, belongs to microaerobic bacteria. We reported a 21-year-old male patient diagnosed with hemophagocytic lymphohistiocytosis (HLH) due to infection, who presented with multiple clinical manifestations of peripheral nerve injury, such as ophthalmoplegia, facial paralysis, and urinary retention during the treatment. Electromyography showed neurogenic injury and the final diagnosis was Guillain-Barre Syndrome (GBS). After treatment of dexamethasone combined with immunoglobulin, the patient was discharged from the hospital with partial recovery of neurological symptoms.

摘要

（）是一种革兰氏阴性菌，属于微需氧菌。我们报告了一名21岁男性患者，因感染被诊断为噬血细胞性淋巴组织细胞增生症（HLH），在治疗期间出现了周围神经损伤的多种临床表现，如眼肌麻痹、面瘫和尿潴留。肌电图显示神经源性损伤，最终诊断为吉兰 - 巴雷综合征（GBS）。经地塞米松联合免疫球蛋白治疗后，患者出院，神经症状部分恢复。