Literature DB >> 16188868

Recurring acute abdominal pains in an adolescent as the presenting manifestations of hereditary angioneurotic oedema.

Laurence Foix-L'Hélias1, Laurence Weiss, Alix Mollet-Boudjemline, David Fallik, Pascale Trioche-Eberschweiler, Philippe Labrune.   

Abstract

UNLABELLED: An adolescent was hospitalized for recurring abdominal pains, which had previously led to appendicectomy. Laboratory data finally led to the diagnosis of hereditary angioneurotic oedema, after several hypotheses had been raised and ruled out.
CONCLUSIONS: Angioneurotic oedema is a rare condition, which should be suspected in children with recurring abdominal pains, especially when there is liquid within the peritoneal cavity.

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Year:  2005        PMID: 16188868     DOI: 10.1111/j.1651-2227.2005.tb02064.x

Source DB:  PubMed          Journal:  Acta Paediatr        ISSN: 0803-5253            Impact factor:   2.299


  3 in total

1.  Pediatric hereditary angioedema due to C1-inhibitor deficiency.

Authors:  Henriette Farkas
Journal:  Allergy Asthma Clin Immunol       Date:  2010-07-28       Impact factor: 3.406

2.  Abdominal and pelvic imaging in the diagnosis of acute abdominal attacks in patients with hereditary angioedema due to C1-inhibitor deficiency.

Authors:  Piotr Obtułowicz; Marcin Stobiecki; Wojciech Dyga; Aldona Juchacz; Tadeusz Popiela; Krystyna Obtułowicz
Journal:  Postepy Dermatol Alergol       Date:  2021-08-13       Impact factor: 1.664

3.  International consensus on the diagnosis and management of pediatric patients with hereditary angioedema with C1 inhibitor deficiency.

Authors:  H Farkas; I Martinez-Saguer; K Bork; T Bowen; T Craig; M Frank; A E Germenis; A S Grumach; A Luczay; L Varga; A Zanichelli
Journal:  Allergy       Date:  2016-09-08       Impact factor: 13.146

  3 in total

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