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1.
Eur J Pediatr ; 169(8): 1029-32, 2010 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-20039062

RESUMO

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.


Assuntos
Doença de Gaucher/diagnóstico , Glucosilceramidase/sangue , Mães/psicologia , Síndrome de Munchausen Causada por Terceiro/complicações , Síndrome de Munchausen Causada por Terceiro/diagnóstico , Anemia/etiologia , Diagnóstico Diferencial , Feminino , Doença de Gaucher/enzimologia , Glucosilceramidase/biossíntese , Hepatomegalia/etiologia , Humanos , Lactente , Relações Mãe-Filho , Síndrome de Munchausen Causada por Terceiro/sangue , Síndrome de Munchausen Causada por Terceiro/psicologia , Síndromes Mielodisplásicas/diagnóstico , Sepse/etiologia , Papel do Doente , Esplenomegalia/etiologia , Trombocitopenia/etiologia
2.
Int J Pediatr Adolesc Med ; 4(2): 51-53, 2017 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-30805501

RESUMO

Celiac disease (CD) is an immune-mediated disease affecting the small intestine secondary to gluten exposure. The currently available treatment is lifelong adherence to a gluten-free diet (GFD). Several disorders are known to be associated with celiac disease, including Down syndrome (DS). In several studies, the prevalence of CD in DS ranged between 4 and 17%. CD is prevalent in Arabs; however, few studies have been performed to determine the prevalence of CD in DS patients. Our study aimed to determine the prevalence of CD in Saudi Down syndrome patients using serological markers and small bowel biopsy. This is a retrospective study in which files relating to Down syndrome patients who were followed up in a general pediatric clinic at King Faisal Specialist Hospital and Research Center were reviewed regarding demographic data, serological markers and biopsy results. Of the total number of patients reviewed (91), 7 were excluded because data were missing; the remaining 84 patients included 35 females and 49 males. The age range of the patients at the time of screening was from 1 to 18 years. Patient demographic data are shown in Table 1. Among the studied patients, antigliadin antibody (AGA) IgA was high in 27 patients (32.14%), and AGA IgG was high in 44 patients (52.38%). Twelve patients (14.28%) tested positive and 58 (69.04%) tested negative for anti-endomysial antibodies. Anti-tissue glutaminase antibody IgA was found to be high in 13 patients (15.5%) and normal in 54 patients (64.28%). Serum IgA levels were normal in 36 patients (43%) and low in 1 patient (1.2%). Biopsy was performed in 22 patients who tested positive for anti-endomysial or anti-tissue transglutaminase antibodies. The biopsies provided positive results in 9 patients (10.7%). Our study showed a confirmed prevalence of 10.7% for celiac disease in Saudi patients with Down syndrome based on serology and biopsy; together with previous cases reported in the literature, this result indicates a need to screen these patients for celiac disease.

3.
Ann Saudi Med ; 33(5): 505-7, 2013.
Artigo em Inglês | MEDLINE | ID: mdl-24188948

RESUMO

The insertion of sewing needles into the abdominal cavity is an uncommon form of child abuse. We report a 2-and-a-half-year-old boy with 2 intra-abdominal sewing needles that were discovered during the evaluation of chronic abdominal pain and vomiting. This case report illustrates the wide range with which abusive injury can present in children. Pediatricians need to be alerted to this newly-recognized and the increasing form of child abuse so that they examine and diagnose their patients appropriately.


Assuntos
Dor Abdominal/etiologia , Maus-Tratos Infantis/diagnóstico , Corpos Estranhos/diagnóstico , Traumatismos Abdominais/diagnóstico , Traumatismos Abdominais/etiologia , Pré-Escolar , Dor Crônica/etiologia , Humanos , Masculino , Agulhas , Vômito/etiologia
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