HSV Encephalomyelitis in an Immunocompetent Patient With Prior Splenectomy.

IF 0.9 Q4 CLINICAL NEUROLOGY
Neurohospitalist Pub Date : 2023-07-01 Epub Date: 2023-05-17 DOI:10.1177/19418744231169406
Destiny Marquez, Raquel Romero, Dana Klavansky, Alexandra S Reynolds
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引用次数: 0

Abstract

A 44-year-old male with history of asplenia, provoked PE, and hyperlipidemia presented with ascending paralysis, bowel and bladder incontinence and altered mental status, and progressively developed acute hypoxic respiratory failure. Initial workup including CT head, magnetic resonance imaging (MRI) brain, and lumbar puncture which was concerning for herpes simplex virus (HSV) meningoencephalitis; out of caution he was started on multiple antibiotics consequently resulting in the development of Clostridium difficile (C.diff). He also received two doses of IVIG. He was transferred to our institution and after interval re-imaging via MRI brain and spinal surveys and repeat lumbar punctures, he was found to have a high CSF HSV titer and positive GAD 65 antibody, the latter likely a false positive due to IVIG administration. IVIG was not continued from the outside hospital due to the development of deep vein thrombosis (DVT), and the risks of plasmapheresis outweighed the benefits. The patient gradually improved after a prolonged course of acyclovir and was downgraded out of the Neuroscience ICU (NSICU), however decompensated due to rectal bleeding, and subsequently went into cardiac arrest. Though this patient underwent a splenectomy, his relative immunocompetency towards non-encapsulated organisms should have been preserved. It has not been clearly described in the literature how and why HSV encephalomyelitis takes a fulminant course in immunocompetent patients, including our asplenic patient. Furthermore, definitive treatment and management of this condition remains unclear. Severity of HSV encephalomyelitis has not been clearly described in the literature, particularly in immunocompetent patients (such as this asplenic patient).

曾接受脾切除术的免疫功能正常患者患上 HSV 脑脊髓炎
一名 44 岁的男性患者,曾患脾大、诱发性肺炎和高脂血症,出现上行性瘫痪、大便和膀胱失禁、精神状态改变,并逐渐发展为急性缺氧性呼吸衰竭。初步检查包括头部 CT、脑部磁共振成像(MRI)和腰椎穿刺,结果显示为单纯疱疹病毒(HSV)脑膜脑炎;出于谨慎,他开始使用多种抗生素,结果导致艰难梭菌(C.diff)感染。他还接受了两剂 IVIG。他被转到我院后,经过磁共振脑部和脊柱检查以及重复腰椎穿刺,发现他的 CSF HSV 滴度很高,GAD 65 抗体呈阳性,后者很可能是由于注射了 IVIG 导致的假阳性。由于出现了深静脉血栓 (DVT),且浆膜穿刺的风险大于益处,因此没有从外院继续注射 IVIG。经过长时间的阿昔洛韦治疗后,患者病情逐渐好转,并从神经科学重症监护室(NSICU)降级,但由于直肠出血而出现失代偿,随后心跳骤停。虽然这名患者接受了脾脏切除术,但他对非包囊生物的相对免疫能力本应得到保留。关于 HSV 脑脊髓炎如何以及为何会在免疫功能正常的患者(包括我们这位脾功能不全的患者)中出现暴发性病程,文献中还没有明确的描述。此外,这种病症的确切治疗和管理方法仍不明确。HSV 脑脊髓炎的严重程度在文献中没有明确描述,尤其是在免疫功能正常的患者(如本例脾功能不全患者)中。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Neurohospitalist
Neurohospitalist CLINICAL NEUROLOGY-
CiteScore
1.60
自引率
0.00%
发文量
108
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