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Management and long-term evolution of a patient with 3-hydroxy-3-methylglutaryl-coenzyme A lyase deficiency.
Muñoz-Bonet, Juan Ignacio; Ortega-Sánchez, María Del Carmen; León Guijarro, José Luis.
Afiliación
  • Muñoz-Bonet JI; Pediatric Intensive Care Unit, Hospital Clínico Universitario, University of Valencia, Av. Blasco Ibáñez 17, 46010, Valencia, Spain. munoz_jua@gva.es.
  • Ortega-Sánchez MD; Department of Pediatrics, Hospital Clínico Universitario, Av. Blasco Ibáñez 17, 46010, Valencia, Spain.
  • León Guijarro JL; Department of Radiology, Hospital Clínico Universitario, Avda. Blasco Ibáñez 17, 46010, Valencia, Spain.
Ital J Pediatr ; 43(1): 12, 2017 Jan 19.
Article en En | MEDLINE | ID: mdl-28257639
ABSTRACT

BACKGROUND:

3-Hydroxy-3-methylglutaryl-coenzyme A (HMG-CoA) lyase deficiency is a rare inborn error of metabolism characterized by recurrent metabolic crises caused by fasting, intercurrent illness and excessive physical exercise. Non ketotic hypoglycemia is normally the cause of primary symptoms but without an immediate treatment the illness can evolve into a worsening metabolic state resembling the Reye's syndrome that may cause the patient's death. We report a case with some clinical and therapeutic features not previously described. CASE PRESENTATION Patient with HMG-CoA lyase deficiency whom after diagnosis at 2 years of age was re-admitted 12 years later, after severe metabolic decompensation following consumption of alcohol. Despite a quick correction of hypoglycemia, within the following few hours, the patient fell into a coma. Suspecting intracranial hypertension (ICH), the patient required mechanical ventilation. Although liver cytolysis was minimal, hyperamoniemia reached 1394 µmol/L, returning to normal, a few hours after administering sodium phenylacetate and sodium benzoate, whose use has not been reported in these patients. Brain edema was evidenced in the computed tomography and by the magnetic resonance imaging that determined that the edema was cytotoxic, as quantified with the restriction of diffusion in the apparent diffusion coefficient map. During the recovery of the ICH, we belatedly, detected vasospasm moderate-severe that was treated with nimodipine. Currently, the patient maintains clinical normality.

CONCLUSIONS:

The alcohol consumption must be avoided in patients with HMG-CoA lyase deficiency. In our patient hyperamoniemia was effectively treated with sodium phenylacetate and sodium benzoate. Magnetic resonance imaging showed and quantified the cytotoxic brain edema. Belatedly, a cerebral vasospasm was an additional mechanism of cerebral injury. None of these observations has been previously reported.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Acetil-CoA C-Acetiltransferasa / Encéfalo / Acilcoenzima A / Manejo de la Enfermedad / Predicción / Errores Innatos del Metabolismo de los Aminoácidos / Glucosa / Hipoglucemia Tipo de estudio: Diagnostic_studies / Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Adolescent / Humans / Male Idioma: En Revista: Ital J Pediatr Asunto de la revista: PEDIATRIA Año: 2017 Tipo del documento: Article País de afiliación: España

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Acetil-CoA C-Acetiltransferasa / Encéfalo / Acilcoenzima A / Manejo de la Enfermedad / Predicción / Errores Innatos del Metabolismo de los Aminoácidos / Glucosa / Hipoglucemia Tipo de estudio: Diagnostic_studies / Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Adolescent / Humans / Male Idioma: En Revista: Ital J Pediatr Asunto de la revista: PEDIATRIA Año: 2017 Tipo del documento: Article País de afiliación: España