Abstract
Hereditary C1 esterase inhibitor deficiency is often associated with immunpathologic disorders. The authors present a case of the rare coincidence of hereditary angioedema (HAE) and Crohn's disease. The history of the patient is analysed along with the familial occurrence of the disease. Characteristic abdominal manifestations of C1 esterase inhibitor deficiency are compared to the clinical signs of Crohn's disease. Differential diagnostic pitfalls are described along with efficatious therapeutic options.
Publication types
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Case Reports
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English Abstract
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Review
MeSH terms
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Adult
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Angioedema / complications
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Angioedema / genetics*
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Angioedema / immunology
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Angioedema / surgery
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Ascites / etiology
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Colectomy / methods
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Colon / pathology
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Complement C1 Inactivator Proteins / deficiency*
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Crohn Disease / complications*
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Crohn Disease / immunology
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Crohn Disease / pathology
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Crohn Disease / surgery
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Diagnosis, Differential
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Humans
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Ileocecal Valve / pathology
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Ileocecal Valve / surgery
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Male
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Pedigree
Substances
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Complement C1 Inactivator Proteins