Munchausen syndrome by proxy mimicking as Gaucher disease.
Eur J Pediatr
; 169(8): 1029-32, 2010 Aug.
Article
em En
| MEDLINE
| ID: mdl-20039062
ABSTRACT
Although rare, Munchausen syndrome by proxy (MBP) is a potentially life-threatening form of child abuse. Here, we report a 19-month-old female infant who presented with hepatosplenomegaly, anemia, thrombocytopenia, and recurrent septicemia. She was initially thought to have myelodysplastic syndrome. Further hematological and immunological investigations revealed no cause. beta-Glucosylceramidase enzyme activity on dried blood spot was suggestive of Gaucher disease. However, the enzyme level on cultured skin fibroblast was not consistent with Gaucher disease. The first hint about MBP was the recurrent sepsis with numerous gram negative rods. Furthermore, the mother's behavior and health history raised our suspicion about MBP. The child showed significant improvement after she was separated from the mother for a week. Finally, the mother confessed that she was spitting in local herbs and injecting it into the central line. This is, to our knowledge, the first report of MBP resembling in its presentation Gaucher disease. This case should alert the general and specialized pediatricians about MBP, as it may mimic metabolic diseases like Gaucher disease.
Texto completo:
1
Base de dados:
MEDLINE
Assunto principal:
Síndrome de Munchausen Causada por Terceiro
/
Doença de Gaucher
/
Glucosilceramidase
/
Mães
Tipo de estudo:
Diagnostic_studies
/
Etiology_studies
Limite:
Female
/
Humans
/
Infant
Idioma:
En
Revista:
Eur J Pediatr
Ano de publicação:
2010
Tipo de documento:
Article
País de afiliação:
Arábia Saudita