Literature DB >> 21933405

Isolated angioedema of the bowel due to C1 esterase inhibitor deficiency: a case report and review of literature.

Shivangi T Kothari1, Anish M Shah, Deviprasad Botu, Robert Spira, Robert Greenblatt, Joseph Depasquale.   

Abstract

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Year:  2011        PMID: 21933405      PMCID: PMC3189146          DOI: 10.1186/1752-1947-5-467

Source DB:  PubMed          Journal:  J Med Case Rep        ISSN: 1752-1947


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Correction

Following the publication of our article [1] an error in the discussion section was noted. In the description of the five phases of abdominal pain attacks associated with classic hereditary angioedema [2], we incorrectly stated the phases and described phase V instead of phase zero. Phase I starts with a period of non-cramping abdominal discomfort followed by (phase II) a crescendo phase which leads to (phase III) severe pain. Phase III is associated with vomiting and occasional diarrhea. Hypovolemia and hemoconcentration can occur as a result of a combination of events including vasodilatation, fluid shifts with edema of the bowel, ascites, and volume depletion related to vomiting and diarrhea. Phase IV refers to a decrescendo phase, which is a self limiting phase for untreated abdominal pain. Phase V refers to the resolution of pain, which can occur as often as twice a week

Should read

Phase zero also known as Prephase which includes fatigue, irritability, sensitivity to noise, nausea, and erythema marginatum. Phase I starts with a period of non-cramping abdominal discomfort followed by (phase II) a crescendo phase which leads to (phase III) severe pain. Phase III is associated with vomiting and occasional diarrhea. Hypovolemia and hemoconcentration can occur as a result of a combination of events including vasodilatation, fluid shifts with edema of the bowel, ascites, and volume depletion related to vomiting and diarrhea. Phase IV refers to a decrescendo phase, which is a self limiting phase for untreated abdominal pain
  2 in total

1.  Symptoms, course, and complications of abdominal attacks in hereditary angioedema due to C1 inhibitor deficiency.

Authors:  Konrad Bork; Petra Staubach; Alexander J Eckardt; Jochen Hardt
Journal:  Am J Gastroenterol       Date:  2006-02-08       Impact factor: 10.864

2.  Isolated angioedema of the bowel due to C1 esterase inhibitor deficiency: a case report and review of literature.

Authors:  Shivangi T Kothari; Anish M Shah; Deviprasad Botu; Robert Spira; Robert Greenblatt; Joseph Depasquale
Journal:  J Med Case Rep       Date:  2011-02-14
  2 in total
  2 in total

1.  C1-esterase inhibitor deficiency in pediatric heart transplant recipients: incidence and findings on ultrasound.

Authors:  Sabine Pabst; Nadja Hamscho; Fritz Roller; Holger Stracke; Dietmar Schranz; Claudia Lämmler; Gerhard Alzen; Gabriele A Krombach
Journal:  Pediatr Radiol       Date:  2013-12-21

2.  Concurrent Paraneoplastic Dermatomyositis and Acquired C1 Esterase Inhibitor Deficiency in Primary Laryngeal Small Cell Carcinoma.

Authors:  Udit Nindra; Katie Nguyen; JunHee Hong; Victoria Bray; Eugene Moylan
Journal:  Case Rep Oncol       Date:  2021-12-23
  2 in total

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