Awaguni Hitoshi, Shinozuka Jun, Tanaka Shin-Ichiro, Kadowaki Sayaka, Makino Shigeru, Maruyama Rikken, Shigematsu Yosuke, Hamaoka Kenji, Imashuku Shinsaku
Division of Pediatrics, Uji-Tokushukai Medical Center, Uji, Kyoto, Japan.
Pediatr Rep. 2018 Mar 29;10(1):7424. doi: 10.4081/pr.2018.7424. eCollection 2018 Mar 22.
Acute encephalopathy with biphasic seizures and late reduced diffusion (AESD) develops in association with systemic as well as central nervous system (CNS) viral or bacterial infections. AESD is most often noted with influenza or human herpesvirus 6 infection in previously healthy infants. However, AESD has also been reported in an infant with developmental retardation and in a mentally and motor-disabled adolescent. Here, we report the case of a 4- year-old female with significant development delay due to spinal muscular atrophy, who developed AESD during sepsis with no apparent CNS infection. Although the patient had extremely high serum procalcitonin (45.84 ng/mL, reference; <0.4) on admission indicating a poor prognosis, she was successfully managed for sepsis and AESD.
伴有双相性癫痫发作和晚期弥散受限的急性脑病(AESD)与全身性以及中枢神经系统(CNS)病毒或细菌感染相关。AESD最常见于既往健康的婴儿感染流感或人类疱疹病毒6型时。然而,也有报道称一名发育迟缓的婴儿以及一名智力和运动残疾的青少年发生了AESD。在此,我们报告一例4岁女性患儿,因脊髓性肌萎缩导致严重发育迟缓,在无明显CNS感染的脓毒症期间发生了AESD。尽管患者入院时血清降钙素原极高(45.84 ng/mL,参考值;<0.4),提示预后不良,但她成功地接受了脓毒症和AESD的治疗。