منابع مشابه
Hereditary Angioedema
Copyright © 2008 Massachusetts Medical Society. A 19-year-old woman presents to the emergency department with light-headedness, severe abdominal pain, and intractable nausea and vomiting that began 12 hours earlier. The patient reports previous episodes of abdominal pain and swelling of her hands and feet that have been attributed possibly to food allergies, which have recently become more freq...
متن کاملA Case of Hereditary Angioedema Presenting with Ileocolic Intussusception
Case Presentation: A 38-year-old female with a past medical history of type 2 HAE presents with seven days of progressive right lower quadrant abdominal pain and distension, nausea, constipation, and decreased oral intake. Unlike her previous HAE episodes, her symptoms persisted despite two icatibant 30 mg subcutaneous injections. At presentation, she was afebrile, normotensive, and non-tachyca...
متن کاملA case of Hereditary Angioedema Associated with Idiopathic Hypoparathyroidism
Hereditary angioedema is a rare autosomal dominant disease characterized by the edema of subcutaneous tissues, respiratory tract and bowel. It is caused by the deficiency of C1 esterase inhibitor. Hereditary angioedema may be associated with autoimmune diseases, such as systemic lupus erythematosus, rheumatoid arthritis, autoimmune thyroiditis and glomerulonephritis. We report a 34-year-old mal...
متن کاملA Case of Type 2 Hereditary Angioedema With SERPING1 Mutation
Hereditary angioedema is a disease of congenital deficiency or functional defect in the C1 esterase inhibitor (C1-INH) consequent to mutation in the SERPING1 gene, which encodes C1-INH. This disease manifests as recurrent, non-pitting, non-pruritic subcutaneous, or submucosal edema as well as an erythematous rash in some cases. These symptoms result from the uncontrolled localized production of...
متن کاملPathophysiology of Hereditary Angioedema.
The genetic deficiency of the C1 inhibitor is responsible for hereditary angioedema (HAE), which is a disease transmitted as an autosomal dominant trait. More than 200 point mutations in the C1 inhibitor gene have been found to be associated with HAE. Patients with this disease suffer from recurrent angioedema, which is mediated by bradykinin derived from activation of the contact system. This ...
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ژورنال
عنوان ژورنال: Nihon Rinsho Geka Gakkai Zasshi (Journal of Japan Surgical Association)
سال: 2015
ISSN: 1345-2843,1882-5133
DOI: 10.3919/jjsa.76.1604