Hereditary angioedema is a rare but serious problem with the immune system that is passed down through families. It causes swelling, particularly of the face and airways, and abdominal cramping. See also: Angioedema
Hereditary angioedema (HAE) is caused by low levels or improper function of a protein called C1 inhibitor. This problem affects the blood vessels. People with hereditary angioedema can develop rapid swelling of the hands, feet, limbs, face, intestinal tract, larynx (voicebox), or trachea (windpipe). There is usually no itching or hives. Swelling of the gut can cause intestinal cramping. If swelling closes the airway, it can be deadly. Attacks of swelling can become more severe in late childhood and adolescence. There is usually a family history of the condition. However, relatives may be unaware of previous cases, which may have just been reported as an unexpected, sudden, and premature death of a parent, aunt, uncle, or grandparent. Dental procedures, sickness (including colds and the flu), and surgery have been shown to trigger certain attacks of hereditary angioedema.
Blood tests will be done to check the levels of C1 inhibiting factor, C4 and C2.
Antihistamines and other related treatments are of limited benefit in hereditary angioedema. Attenuated androgens, which are derivatives of normal sex hormones, can reduce the frequency and severity of attacks. Once an attack occurs, treatment includes pain relief and fluids given by an intravenous (IV) line. Helicobacter pylori, a bacteria found in the stomach, can trigger abdominal attacks. Getting rid of the bacteria with antibiotic therapy decreases these abdominal attacks.
Hereditary angioedema can be life threatening and treatment options are limited. How well a person does depends on the individual's specific symptoms.
Swelling of the airways may be deadly.
|
|
Reviewer Info: David C. Dugdale, III, MD, Professor of Medicine, Division of General Medicine, Department of Medicine, University of Washington School of Medicine; and Stuart I. Henochowicz, MD, FACP, Associate Clinical Professor of Medicine, Division of Allergy, Immunology, and Rheumatology, Georgetown University Medical School. Also reviewed by David Zieve, MD, MHA, Medical Director, A.D.A.M., Inc. ; ADAM Health Illustrated Encyclopedia, 05/01/2008 |