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1.
Pediatr Int ; 55(3): e77-80, 2013 Jun.
Article in English | MEDLINE | ID: mdl-23782386

ABSTRACT

Here we report the case of a 9-year-old boy with acute respiratory distress syndrome (ARDS) caused by novel H1N1 swine-origin influenza virus A. A diagnosis of ARDS caused by a novel influenza A (H1N1) virus was made on the basis of chest X-ray and computed tomography together with low oxygenation index (OI) and the detection of novel influenza A (H1N1) virus from tracheal secretion samples. Oseltamivir phosphate and prone positioning were effective in the treatment of ARDS in this case. These findings suggest that anti-viral drugs and prone positioning can play an important role in the improvement of ARDS caused by novel H1N1 swine-origin influenza virus A.


Subject(s)
Antiviral Agents/therapeutic use , Influenza A Virus, H1N1 Subtype , Influenza, Human/therapy , Oseltamivir/therapeutic use , Pandemics , Prone Position , Respiratory Distress Syndrome/therapy , Child , Combined Modality Therapy , Humans , Influenza, Human/diagnosis , Male , Oxygen/blood , Respiratory Distress Syndrome/diagnosis , Tomography, X-Ray Computed
2.
Brain Dev ; 32(8): 669-72, 2010 Sep.
Article in English | MEDLINE | ID: mdl-19783111

ABSTRACT

We report an adolescent case of late-onset riboflavin-responsive multiple acyl-CoA dehydrogenase deficiency (MADD) characterized by intermittent nausea and depressive state as early symptoms. At the age of 12 years and 11 months, the patient experienced intermittent nausea and vomiting, and depressive state. She was on medication for depression for 5 months but it was ineffective. Brain magnetic resonance imaging showed disseminated high-intensity areas in the periventricular white matter and in the splenium of the corpus callosum on T2-weighted images and fluid-attenuated inversion-recovery images. Progressive muscle weakness occurred and blood creatine kinase level was found to be elevated. The muscle biopsy revealed lipid storage myopathy. Urine organic acid analysis and mutation analysis of the ETFDH gene confirmed the diagnosis of MADD. With oral supplements of riboflavin and l-carnitine, in addition to a high-calorie and reduced-fat diet, her clinical symptoms improved dramatically. Early diagnosis is important because riboflavin treatment has been effective in a significant number of patients with MADD.


Subject(s)
Central Nervous System/physiopathology , Multiple Acyl Coenzyme A Dehydrogenase Deficiency/diet therapy , Multiple Acyl Coenzyme A Dehydrogenase Deficiency/diagnosis , Muscle, Skeletal/physiopathology , Riboflavin/therapeutic use , Adolescent , Age of Onset , Biopsy , Central Nervous System/pathology , Electron-Transferring Flavoproteins/deficiency , Electron-Transferring Flavoproteins/genetics , Female , Humans , Iron-Sulfur Proteins/deficiency , Iron-Sulfur Proteins/genetics , Multiple Acyl Coenzyme A Dehydrogenase Deficiency/enzymology , Multiple Acyl Coenzyme A Dehydrogenase Deficiency/genetics , Muscle, Skeletal/pathology , Muscle, Skeletal/surgery , Oxidoreductases Acting on CH-NH Group Donors/deficiency , Oxidoreductases Acting on CH-NH Group Donors/genetics , Treatment Outcome
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