Acute Necrotizing Encephalopathy of Childhood: A Multicenter Experience in Saudi Arabia

被引:34
作者
Bashiri, Fahad A. [1 ]
Al Johani, Sultan [1 ]
Hamad, Muddathir H. [1 ]
Kentab, Amal Y. [1 ]
Alwadei, Ali H. [2 ]
Hundallah, Khalid [3 ]
Hasan, Hamdi H. [4 ]
Alshuaibi, Walaa [5 ]
Jad, Lamyaa [2 ]
Alrifai, Muhammad Talal [6 ]
Hudairi, Abrar [1 ]
Al Sheikh, Rana [1 ]
Alenizi, Asma'a [3 ]
Alharthi, Nawaf A. [7 ]
Abdelmagid, Tayseer A. [8 ]
Ba-Armah, Duaa [6 ]
Salih, Mustafa A. [1 ]
Tabarki, Brahim [3 ]
机构
[1] King Saud Univ, Div Pediat Neurol, Dept Pediat, Coll Med, Riyadh, Saudi Arabia
[2] King Fahd Med City, Natl Neurosci Inst, Pediat Neurol Dept, Riyadh, Saudi Arabia
[3] Prince Sultan Mil Med City, Div Pediat Neurol, Dept Pediat, Riyadh, Saudi Arabia
[4] King Saud Univ, Neuroradiol Div, Dept Radiol, Coll Med, Riyadh, Saudi Arabia
[5] King Saud Univ, King Khalid Univ Hosp, Med Genet Div, Dept Pediat,Coll Med, Riyadh, Saudi Arabia
[6] King Abdul Aziz Med City, King Abdullah Children Hosp, Div Neurol, Pediat Dept,Minist Natl Guard, Riyadh, Saudi Arabia
[7] Princess Nourah Bint Abdulrahman Univ, King Abdullah bin Abdulaziz Univ Hosp, Coll Med, Pediat Dept, Riyadh, Saudi Arabia
[8] Armed Forces Hosp Southern Reg, Dept Pediat, Khamis Mushayt, Saudi Arabia
关键词
necrotizing encephalopathy; children; seizure; influenza virus; RANBP2; gene; BILATERAL THALAMIC NECROSIS; INFLUENZA-A; RANBP2; INFECTION; MUTATION; CHILDREN; INFANTS; FAMILY;
D O I
10.3389/fped.2020.00526
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Background: Acute necrotizing encephalopathy of childhood (ANEC) is a rapidly progressing encephalopathy characterized by fever, depressed level of consciousness, and seizures. Diagnosis depends on clinical presentation and characteristic neuroimaging findings of abnormal signal intensity involving the thalami as well as the supra and infra-tentorial areas. Treatment modalities are not well-established; empirical treatment with antibiotics and antiviral agents is the initial step, followed by steroids and immunoglobulin, as well as supportive care. Patients with ANEC have a variable prognosis, but mortality is very high. Methods: A retrospective chart review of patients diagnosed with ANEC in five tertiary centers from January 2015 to October 2018 was performed. Clinical and radiological findings, as well as the therapeutic approach and outcomes, were described. Results: Twelve children were included ranging in age from 10 months to 6 years. All patients presented with preceding febrile illness, altered level of consciousness, and seizure. Radiological features showed abnormal signals in the thalami, and five patients (41.7%) had brainstem involvement. All patients received empirical treatment with antibiotics and antiviral agents. Ten patients (83.3%) received intravenous immunoglobulin (IVIG) and IV Methylprednisolone therapy. Outcomes were variable ranging from good outcomes with minimal neurological deficits to poor outcomes and death in 25% of cases. Conclusion: ANEC is a rare fulminant disease in children. The treatment is challenging. Early interventions with the use of IVIG and IV Methylprednisolone may change the outcome; however, further studies are needed to establish a consensus guideline for the management.
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页数:9
相关论文
共 29 条
[1]   H1N1 TRIGGERED RECURRENT ACUTE NECROTIZING ENCEPHALOPATHY IN A FAMILY WITH A T653I MUTATION IN THE RANBP2 GENE [J].
Anand, Geetha ;
Visagan, Ravindran ;
Chandratre, Saleel ;
Segal, Shelley ;
Nemeth, Andrea H. ;
Squier, Waney ;
Sheerin, Fintan ;
Neilson, Derek ;
Jayawant, Sandeep .
PEDIATRIC INFECTIOUS DISEASE JOURNAL, 2015, 34 (03) :318-320
[2]  
Campistol J, 1998, DEV MED CHILD NEUROL, V40, P771, DOI 10.1111/j.1469-8749.1998.tb12346.x
[3]   RANBP2 is an allosteric activator of the conventional kinesin-1 motor protein, KIF5B, in a minimal cell-free system [J].
Cho, Kyoung-in ;
Yi, Haiqing ;
Desai, Ria ;
Hand, Arthur R. ;
Haas, Arthur L. ;
Ferreira, Paulo A. .
EMBO REPORTS, 2009, 10 (05) :480-486
[4]   Familial acute necrotizing encephalopathy due to mutation in the RANBP2 gene [J].
Denier, Christian ;
Balu, Laurent ;
Husson, Beatrice ;
Nasser, Ghaidaa ;
Burglen, Lydie ;
Rodriguez, Diana ;
Labauge, Pierre ;
Chevret, Laurent .
JOURNAL OF THE NEUROLOGICAL SCIENCES, 2014, 345 (1-2) :236-238
[5]   Postinfectious family case of acute necrotizing encephalopathy caused by RANBP2 gene mutation [J].
Di Meglio, C. ;
Cano, A. ;
Milh, M. ;
Girard, N. ;
Burglen, L. ;
Chabrol, B. .
ARCHIVES DE PEDIATRIE, 2014, 21 (01) :73-77
[6]   Recurrent acute necrotizing encephalopathy following influenza A in a genetically predisposed family [J].
Gika, Artemis D. ;
Rich, Philip ;
Gupta, Sachin ;
Neilson, Derek E. ;
Clarke, Antonia .
DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY, 2010, 52 (01) :99-102
[7]   Acute necrotizing encephalopathy of childhood associated with influenza type B virus infection in a 3-year-old girl [J].
Huang, SM ;
Chen, CC ;
Chiu, PC ;
Lai, PH ;
Hsieh, KS .
JOURNAL OF CHILD NEUROLOGY, 2004, 19 (01) :64-67
[8]   Serum cytokine concentrations of influenza-associated acute necrotizing encephalopathy [J].
Ichiyama, T ;
Endo, S ;
Kaneko, M ;
Isumi, H ;
Matsubara, T ;
Furukawa, S .
PEDIATRICS INTERNATIONAL, 2003, 45 (06) :734-736
[9]  
Ito Y, 1999, J MED VIROL, V58, P420, DOI 10.1002/(SICI)1096-9071(199908)58:4<420::AID-JMV16>3.0.CO
[10]  
2-T