XLP1的EBV感染仅表现为行为攻击和利妥昔单抗的有效治疗。

Pub Date : 2018-06-07 eCollection Date: 2018-01-01 DOI:10.1155/2018/3705376
Michelle M Korah-Sedgwick, Luke A Wall
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引用次数: 0

摘要

患有x连锁淋巴细胞增生性疾病1 (XLP1)的患者非常容易感染eb病毒(EBV),首次感染EBV通常导致快速死亡。一名5岁的XLP1患者仅表现为行为攻击,没有器官功能障碍或炎症的实验室证据。虽然EBV- igm阴性,但PCR证实血液和脑脊液中都存在EBV。脑部核磁共振显示额叶病灶。在用更昔洛韦根除他的病毒血症失败后,使用了利妥昔单抗。第二次输注利妥昔单抗后,EBV从血液中被根除,并在5个月后没有出现EBV,此时患者接受了造血干细胞移植。虽然EBV通常会在XLP1患者中产生暴发性感染,但本病例表明EBV感染最初可能很微妙。行为的急剧变化应立即进行评估。该病例也证明了利妥昔单抗治疗急性EBV感染的可能有效性。
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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EBV Infection in XLP1 Manifested Solely by Behavioral Aggression and Effective Treatment Using Rituximab.

Patients with X-linked lymphoproliferative disease 1 (XLP1) are exquisitely susceptible to Epstein-Barr virus (EBV), with the first EBV infection often resulting in rapid death. In a manner not previously described, a 5-year-old patient with XLP1 presented solely with behavioral aggression, with no laboratory evidence of organ dysfunction or inflammation. Although EBV-IgM was negative, PCR confirmed the presence of EBV in both the blood and cerebrospinal fluid. MRI of the brain showed frontal lobe foci. After failure to eradicate his viremia with ganciclovir, rituximab was administered. EBV was eradicated from the blood after the second rituximab infusion and remained absent for 5 months, at which time he underwent hematopoietic stem cell transplant. Although EBV classically produces fulminant infection in patients with XLP1, this case demonstrates that EBV infection may be initially subtle. Acute change in behavior should prompt evaluation. This case also demonstrates the possible effectiveness of rituximab in the treatment of acute EBV infection.

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