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静脉注射免疫球蛋白诱发皮肌炎患者无菌性脑膜炎

Intravenous Immunoglobulin-Induced Aseptic Meningitis in a Dermatomyositis Patient.

作者信息

Rosoph Leah, Ladel Luisa, Patel Ronak, Webster Patrick

机构信息

Internal Medicine, Yale University School of Medicine, Internal Medicine Residency Program at Norwalk Hospital, Norwalk, USA.

Rheumatology, Norwalk Hospital, Norwalk, USA.

出版信息

Cureus. 2024 Apr 14;16(4):e58242. doi: 10.7759/cureus.58242. eCollection 2024 Apr.

Abstract

Aseptic meningitis is a rare but serious complication of treatment with intravenous immunoglobulin (IVIG) and often mimics meningitis of infectious etiology which poses a challenge for timely diagnosis. Although there are published recommendations on the management of IVIG-induced complications, there are no clear guidelines on the continuation of IVIG use after resolution of aseptic meningitis. We present a case of IVIG-induced aseptic meningitis in a patient with a history of refractory dermatomyositis who had been treated with immunosuppressive therapy and IVIG infusions for over a year. The patient developed intense head and neck pain with associated photophobia 24 hours after the most recent IVIG infusion. The patient was managed with supportive care consisting of intravenous fluids and analgesics. The patient's aseptic meningitis resolved without neurological complications. Ultimately, the patient was restarted on IVIG due to the recurrence of weakness from dermatomyositis. The patient tolerated re-initiation of IVIG without recurrence of IVIG-induced complications. This case highlights the importance of considering IVIG-induced aseptic meningitis as a differential diagnosis in evaluating patients with non-infectious meningitis even after regular IVIG infusions. This case also demonstrates that it is safe to reinitiate IVIG after the resolution of IVIG-induced aseptic meningitis.

摘要

无菌性脑膜炎是静脉注射免疫球蛋白(IVIG)治疗的一种罕见但严重的并发症,常酷似感染性病因的脑膜炎,这对及时诊断构成挑战。尽管已有关于IVIG诱导并发症管理的建议,但对于无菌性脑膜炎消退后IVIG使用的继续与否尚无明确指南。我们报告一例有难治性皮肌炎病史的患者发生IVIG诱导的无菌性脑膜炎,该患者接受免疫抑制治疗和IVIG输注已超过一年。在最近一次IVIG输注后24小时,患者出现剧烈的头颈疼痛并伴有畏光。患者接受了包括静脉补液和止痛药物在内的支持治疗。患者的无菌性脑膜炎消退,未出现神经系统并发症。最终,由于皮肌炎导致的肌无力复发,患者重新开始使用IVIG。患者耐受了IVIG的重新使用,未出现IVIG诱导并发症的复发。该病例强调了即使在常规IVIG输注后,在评估非感染性脑膜炎患者时将IVIG诱导的无菌性脑膜炎作为鉴别诊断的重要性。该病例还表明,IVIG诱导的无菌性脑膜炎消退后重新开始使用IVIG是安全的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0740/11093182/c3c1d59352ad/cureus-0016-00000058242-i01.jpg

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