Literature DB >> 23204705

Hereditary angioedema-presenting as recurrent abdominal pain.

Madhura Milind Killedar1, Anand S Malani.   

Abstract

We report a very rare case of HEREDITARY ANGIOEDEMA, presenting as recurrent acute abdomen. A 22 yr old Maharastrian male, law college student, got admitted for about fifteen times in previous three years for severe, acute onset, upper abdominal pain, vomiting, distention and acute exudative inflammatory ascites .The whole episode used to subside spontaneously within 2-3 days with or without conservative general management .He underwent various investigations from far basic type, to advanced and invasive type with each recurrence but without definitive diagnosis. He also underwent unnecessary appendectomy. The authors did a review of his previous records, but didn't find any definite surgical or medical cause for his acute abdomen. Obviously it was something rare. Authors did search for it in various surgical and medical literature and searched extensively on internet for rare causes of abdominal pain which guided them for further appropriate investigations and diagnose him as a case of HEREDITARY ANGIOEDEMA ,as his clinical features and C1-INH,C3-C4 levels were strongly in favour of it . It goes without saying that the internet has become a standard accessory to conventional literature for cases with diagnostic dilemmas and for treatment options as well.

Entities:  

Keywords:  Acquired angioedema; Hereditary angioedema; Hereditory angioneurotic oedema; Recurrent abdominal pain

Year:  2011        PMID: 23204705      PMCID: PMC3236260          DOI: 10.1007/s12262-011-0255-0

Source DB:  PubMed          Journal:  Indian J Surg        ISSN: 0973-9793            Impact factor:   0.656


  8 in total

1.  Hereditary angioneurotic edema.

Authors:  A K Baranwal; S Singh; L Kumar
Journal:  Indian Pediatr       Date:  1999-02       Impact factor: 1.411

2.  Hereditary angioedema: the clinical syndrome and its management.

Authors:  M M Frank; J A Gelfand; J P Atkinson
Journal:  Ann Intern Med       Date:  1976-05       Impact factor: 25.391

3.  Treatment of hereditary angioedema with a vapor-heated C1 inhibitor concentrate.

Authors:  A T Waytes; F S Rosen; M M Frank
Journal:  N Engl J Med       Date:  1996-06-20       Impact factor: 91.245

4.  Long-term treatment of hereditary angioedema with attenuated androgens: a survey of a 13-year experience.

Authors:  M Cicardi; L Bergamaschini; M Cugno; E Hack; G Agostoni; A Agostoni
Journal:  J Allergy Clin Immunol       Date:  1991-04       Impact factor: 10.793

Review 5.  Angioedema: 5 years' experience, with a review of the disorder's presentation and treatment.

Authors:  C A Megerian; J E Arnold; M Berger
Journal:  Laryngoscope       Date:  1992-03       Impact factor: 3.325

6.  Treatment of hereditary angioedema with danazol. Reversal of clinical and biochemical abnormalities.

Authors:  J A Gelfand; R J Sherins; D W Alling; M M Frank
Journal:  N Engl J Med       Date:  1976-12-23       Impact factor: 91.245

7.  Long-term prophylaxis with C1-inhibitor (C1 INH) concentrate in patients with recurrent angioedema caused by hereditary and acquired C1-inhibitor deficiency.

Authors:  K Bork; G Witzke
Journal:  J Allergy Clin Immunol       Date:  1989-03       Impact factor: 10.793

8.  Hereditary angio-oedema: new clinical observations and autoimmune screening, complement and kallikrein-kinin analyses.

Authors:  E W Nielsen; J T Gran; B Straume; O J Mellbye; H T Johansen; T E Mollnes
Journal:  J Intern Med       Date:  1996-02       Impact factor: 8.989

  8 in total
  1 in total

1.  Consider Hereditary Angioedema in the Differential Diagnosis for Unexplained Recurring Abdominal Pain.

Authors:  Kyle Staller; Anthony Lembo; Aleena Banerji; Jonathan A Bernstein; Eric D Shah; Marc A Riedl
Journal:  J Clin Gastroenterol       Date:  2022-08-15       Impact factor: 3.174

  1 in total

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