[Macroamylasemia: one pediatric case].
Identifieur interne : 000141 ( Ncbi/Merge ); précédent : 000140; suivant : 000142[Macroamylasemia: one pediatric case].
Auteurs : I. Daire [France] ; C. Parrod ; M. Devanlay ; A. Duquenoy ; P. Le Roux ; B. Le LuyerSource :
- Archives de pediatrie : organe officiel de la Societe francaise de pediatrie [ 0929-693X ] ; 2006.
English descriptors
- KwdEn :
- Abdominal Pain (etiology), Adult, Age Factors, Amylases (blood), Amylases (urine), Child, Child, Preschool, Female, Follow-Up Studies, Hematemesis (etiology), Humans, Hyperamylasemia (blood), Hyperamylasemia (diagnosis), Hyperamylasemia (epidemiology), Hyperamylasemia (urine), Male, Prevalence, Sex Factors, Time Factors.
- MESH :
- chemical , blood : Amylases.
- blood : Hyperamylasemia.
- diagnosis : Hyperamylasemia.
- epidemiology : Hyperamylasemia.
- etiology : Abdominal Pain, Hematemesis.
- chemical , urine : Amylases, Hyperamylasemia.
- Adult, Age Factors, Child, Child, Preschool, Female, Follow-Up Studies, Humans, Male, Prevalence, Sex Factors, Time Factors.
Abstract
We report a case of macroamylasemia in an 11-year-old boy. We compare our clinical and paraclinical data with those described in pediatric literature. Macroamylase resulted in a complex of amylase and immuglobulin. Its fortuitous detection did not reveal, up to now, any associated pathology, in particular any autoimmune disorders or celiac disease. Identification of this biochemical abnormality is essential in order to avoid invasive investigations and/or unnecessary therapies.
DOI: 10.1016/j.arcped.2004.12.022
PubMed: 16434172
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pubmed:16434172Le document en format XML
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<term>Amylases (urine)</term>
<term>Child</term>
<term>Child, Preschool</term>
<term>Female</term>
<term>Follow-Up Studies</term>
<term>Hematemesis (etiology)</term>
<term>Humans</term>
<term>Hyperamylasemia (blood)</term>
<term>Hyperamylasemia (diagnosis)</term>
<term>Hyperamylasemia (epidemiology)</term>
<term>Hyperamylasemia (urine)</term>
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<front><div type="abstract" xml:lang="en">We report a case of macroamylasemia in an 11-year-old boy. We compare our clinical and paraclinical data with those described in pediatric literature. Macroamylase resulted in a complex of amylase and immuglobulin. Its fortuitous detection did not reveal, up to now, any associated pathology, in particular any autoimmune disorders or celiac disease. Identification of this biochemical abnormality is essential in order to avoid invasive investigations and/or unnecessary therapies.</div>
</front>
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<ArticleTitle>[Macroamylasemia: one pediatric case].</ArticleTitle>
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<Abstract><AbstractText>We report a case of macroamylasemia in an 11-year-old boy. We compare our clinical and paraclinical data with those described in pediatric literature. Macroamylase resulted in a complex of amylase and immuglobulin. Its fortuitous detection did not reveal, up to now, any associated pathology, in particular any autoimmune disorders or celiac disease. Identification of this biochemical abnormality is essential in order to avoid invasive investigations and/or unnecessary therapies.</AbstractText>
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