Literature DB >> 1504426

Hereditary angioedema: a case with ascites yet no symptoms in the family.

T Shinzato1, H Nakamura, T Kuniyoshi, A Higashionna, T Uehara, J Oshiro, H Uechi, K Shikiya, H Sakugawa, F Kinjo.   

Abstract

An interesting case of hereditary angioedema in a 26-year-old female is reported, with a finding of transient effusion of fluid into the peritoneal cavity during the attacks. The patient suffered from recurrent abdominal pain for several years, but no family members had any similar symptoms. In spite of repeated hospital admissions and many examinations, accurate diagnosis was not made until the most recent admission. The recognition of hereditary angioedema as a cause of acute and/or recurrent abdominal pain may avoid useless invasive procedures and lead to adequate treatment in other similar cases.

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Year:  1992        PMID: 1504426     DOI: 10.2169/internalmedicine.31.633

Source DB:  PubMed          Journal:  Intern Med        ISSN: 0918-2918            Impact factor:   1.271


  3 in total

1.  Hereditary angioedema presenting with recurrent ascites.

Authors:  Rada Jesic; Djordje Culafic; Branka Bonaci-Nikolic
Journal:  Dig Dis Sci       Date:  2005-01       Impact factor: 3.199

Review 2.  Angioedema. Pathogenesis, differential diagnosis, and treatment.

Authors:  Evangelo Frigas; Ugochukwu C Nzeako
Journal:  Clin Rev Allergy Immunol       Date:  2002-10       Impact factor: 8.667

3.  Successful use of daily intravenous infusion of C1 esterase inhibitor concentrate in the treatment of a hereditary angioedema patient with ascites, hypovolemic shock, sepsis, renal and respiratory failure.

Authors:  Hoang Pham; Stephanie Santucci; William H Yang
Journal:  Allergy Asthma Clin Immunol       Date:  2014-12-11       Impact factor: 3.406

  3 in total

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