A Fatal Case of Acute Encephalopathy in a 8-year-old girl from a Pandemic of Influenza A( H1N1) in 2009
スポンサーリンク
概要
- 論文の詳細を見る
We report on a case in which a child died from acute encephalopathy associated with Influenza A( H1N1)pdm. The case pertains to an 8-year-old girl, who was diagnosed with influenza A on the previous day andwas prescribed zanamivir hydrate. She experienced abdominal pain and delirium the next morning, so shewas referred to our hospital. Her level of consciousness at the time of consultation was JCS 200. In the brainCT scan, a swollen brain stem and bilateral middle cerebral artery were depicted. She was in a state of respiratoryfailure, and was admitted to the intensive care unit. She was diagnosed with acute encephalopathycaused by Influenza A, and therapeutic brain hypothermia as well as steroid pulse therapy were performed;however, she died on the third day after hospitalization from multiple organ failure.
- 2011-07-25
著者
-
Imataka George
獨協医科大学 医学部小児科
-
Imataka George
Department Of Pediatrics 1 Neurosurgery 2 And Radiology 3 Dokkyo Medical University School Of Medici
-
George Imataka/eisei
Department Of Pediatrics Dokkyo Medical University School Of Medicine/critial Care & Medicine Do
-
Miyamoto Kenji
Department Of Biosciences And Informatics Center For Biosciences And Informatics Keio University
-
Sato Yuya
Department Of Biotechnology The University Of Tokyo
-
Arisaka Osamu
Department of Pediatrics ,Dokkyo Medical University School of Medicine
-
Watanabe Yoshimitsu
Department of Pediatrics, Dokkyo Medical University School of Medicine
-
Tsukada Keiko
Department of Pediatrics, Dokkyo Medical University School of Medicine
-
Miyamoto Kenji
Department of Pediatrics, Dokkyo Medical University School of Medicine
-
Eisei Hoshiyama
Critial care & Medicine, Dokkyo Medical University School of Medicine
-
Eisei Hoshiyama
Critial care & Medicine, Dokkyo Medical University School of Medicine
-
Imataka George
Department of Pediatrics ,Dokkyo Medical University School of Medicine
-
Tsukada Keiko
Department of Pediatrics, Dokkyo Medical University
関連論文
- Lennox-Gastaut Syndrome Associated with Unilateral Hemispheric Porencephaly
- Image Analysis with the Brain Easy Analysis Tool (BEAT) Method in Cases of Encephalomalacia Following Shaken Baby Syndrome
- Three Cases of Shaken Baby Syndrome withouta History of Shaking
- Down syndrome with acute epiglottitis
- An analysis of epilepsy with chromosomal abnormalities
- Clinical features and subdural lesions in childhood onset Haemophilus influenzae meningitis
- Clinical and Genetic Analyses of Presumed Shwachman-Diamond Syndrome in Japan
- Genetic Diversity of Borrelia burgdorferi Sensu Lato Isolated in Far Eastern Russia
- Severe focal dermal hypoplasia in a female patient transmitted from a mildly affected mother
- Relationship between the Presence of Small, Dense Low-density Lipoprotein and Plasma Lipid Phenotypes in Japanese Children
- Lissencephaly Type I Associated with Lennox-Gastaut Syndrome in a 20-Year-old man : a Case Report
- Clustered Tonic Spasms Developed after Disappearance of Hypsarrythmia in West Syndrome
- Bone Mineral Density in Precocious Puberty
- Anterior Spinal Artery Syndrome in 13-year Old boy:A Case Report
- Comparative Study of Skin Permeation Profiles between Brand and Generic Tulobuterol Patches
- A neuroactive steroid, allotetrahydrocorticosterone inhibits sensory nerves activation in guinea-pig airways
- The Cannabinoid Receptor Agonist WIN 55212-2 Inhibits Neurogenic Inflammations in Airway Tissues
- Long-acting β_2-adrenergic receptor agonist in pediatric asthma
- Brown-Sequard Syndrome in an 8-year-old Girl : a Case Report
- インターネットを用いた小児気管支喘息における在宅の吸入治療状況の調査
- Ultrastructural and cytochemical characterization of human cord blood cells
- Docetaxel-induced apoptosis in the mitotic phase: electron microscopic and cytochemical studies of human leukemia cells
- Sequence Analysis of Thyroid Transcription Factor-2 (TTF-2) Gene in Ten Patients with Congenital Hypothyroidism due to Thyroid Dysgenesis
- 不登校児の診断時におけるストレス・バロメーター
- P-15 Structure and characterization of three enone reductases from Nicotiana tabacum
- Purification and Characterization of Arylmalonate Decarboxylase from Achromobacter sp. KU1311(ENZYMOLOGY, PROTEIN ENGINEERING, AND ENZYME TECHNOLOGY)
- Stereochemistry of Decarboxylation of Arylmalonate Catalyzed by Mutant Enzymes
- The Aldol Type Reaction Catalyzed by Arylmalonate Decarboxylase : A Decarboxylase can Catalyze an Entirely Different Reaction, Aldol Reaction
- A Case of Schizencephaly Type I Associated with West Syndrome that Responded to ACTH Treatment
- Schizencephaly Type I : Magnetic Resonance Imaging and Single Photon Emission Computed Tomography Features
- Discrepancies between Physician and Parent Perceptions of Psychosocial Problems of GHD Children Undergoing GH Therapy in Japan
- Hypocalcemia due to tubular dysfunction in a patient with holoprosencephaly
- A patient with membranoproliferative glomerulonephritis diagnosed by the third biopsy via endocapillary proliferative glomerulonephritis and focal membranoproliferative glomerulonephritis
- A Case of Precocious Puberty Associated with Growth Hormone Deficiency Resulting from Optic Glioma
- Systemic effects of transdermal testosterone for the treatment of microphallus in children
- Skeletal effects of short-term prednisolone therapy in children with steroid-responsive nephrotic syndrome
- Pubertal Progression in Patients with Autonomously Functioning Ovarian Cyst
- Skeletal effects of low-dose cyclosporin A therapy in children with nephrotic syndrome
- Effect of Testosterone on Bone Mineral Gain : Observations of Male Patients with Growth Hormone Deficiency and Normal Gonadotropin Secretion
- Callosal agenesis followed postnatally after prenatal diagnosis
- The Effect of Growth Hormone Therapy on Low-Density Lipoprotein Particle Size
- The Course of Body Mass Index from Infancy to Childhood: Are There Any Properties of Adipose Development that Predispose to Obesity?
- Antiphospholipid antibody syndrome followed by systemic lupus erythematosus in a young male with clinical manifestations since infancy
- Case of incidentally diagnosed vitamin D deficiency rickets : A review of literature from Japan and a proposal for reintroduction of vitamin D_2
- Clinical Case of Brain Sexual Differentiation : As Investigated in Children's Figure Drawing
- Electroencephalography-Guided Resection of Dysembryoplastic Neuroepithelial Tumor
- Dandy-Walker syndrome and chromosomal abnormalities
- MRA Diagnosis of Down Syndrome Associated with Moyamoya Syndrome Presenting Multiple Cerebral Infarctions in a 1-year-old Girl
- Acute Necrotizing Encephalopathy of Childhood due to Influenza Type A Virus
- A Patient with Influenza A-associated Encephalopathy Treated with Mild Hypothermic Therapy and Methylprednisolone Pulse Therapy
- Diastolic flow velocity of the left pulmonary artery of patent ductus arteriosus in preterm infants
- A Fatal Case of Acute Encephalopathy in a 8-year-old girl from a Pandemic of Influenza A( H1N1) in 2009
- Inhibitory Effects of Bakuchiol, Bavachin, and Isobavachalcone Isolated from Piper longum on Melanin Production in B16 Mouse Melanoma Cells
- Congenital cystic periventricular leukomalacia in a small-for-gestational age full-term infant
- Outcome of acute necrotizing encephalopathy in relation to treatment with corticosteroids and gammaglobulin
- Asymmetric Hydrolysis of 1-Cyanoalkyl Acetates(Organic Chemistry)
- Urinary 17-Hydroxycorticosteroids and 17-Ketosteroid Sulfates in Normal Children and in Children with Atopic Dermatitis or Renal Disease
- Relationship between fluvoxamine and stress barometer for nocturnal enuresis
- Bone Maturation and Bone Mineralization in Precocious Puberty
- 超早産児の一過性低サイロキシン血症に対するサイロキシン投与と脳性麻痺
- Detecting weak protein-protein interactions by modified far-western blotting(METHODS)
- Purification and Characterization of the Alcohol Dehydrogenase with a Broad Substrate Specificity Originated from 2-Phenylethanol-Assimilating Brevibacterium sp. KU 1309(ENZYMOLOGY, PROTEIN ENGINEERING, AND ENZYME TECHNOLOGY)
- Clinically Mild form of Joubert Syndrome-related Disorder in a 7-year-old Female:A case report
- Detecting weak protein-protein interactions by modified far-western blotting
- Construction of a Metagenomic Library for the Marine Sponge Halichondria okadai
- A Case of the Kugelberg-Welander Syndrome Complicated with Cardiac Lesions
- Isolation of 9-Hydroxy-10E, 12Z-octadecadienoic Acid, an Inhibitor of Fat Accumulation from Valeriana fauriei
- Transcriptome Analyses of Metabolic Enzymes in Thiosulfate- and Hydrogen-Grown Hydrogenobacter thermophilus Cells