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  2. Acquired C1 esterase inhibitor deficiency - Wikipedia

    en.wikipedia.org/wiki/Acquired_C1_esterase...

    Treatment of acquired angioedema is separated into two main parts. First controlling acute symptoms during angioedema attacks is crucial for preventing and lowering the risk of mortality. [20] Second, managing AAE chronically with prophylactic treatment is important to improve prognosis and quality of life. [20]

  3. Angioedema - Wikipedia

    en.wikipedia.org/wiki/Angioedema

    Angioedema of half of the tongue Angioedema of the face, most strikingly in the upper lip. The skin of the face, normally around the mouth, and the mucosa of the mouth and/or throat, as well as the tongue, swell over the period of minutes to hours. The swelling can also occur elsewhere, typically in the hands. The swelling can be itchy or ...

  4. Type I hypersensitivity - Wikipedia

    en.wikipedia.org/wiki/Type_I_hypersensitivity

    If multiple systems are involved, then anaphylaxis can take place, which is an acute, systemic reaction that can prove fatal. Treatment usually involves adrenaline ( epinephrine ) because it counteracts anaphylaxis by increasing blood flow and relaxing bronchial muscles that block one’s airways. [ 7 ]

  5. Chronic spontaneous urticaria - Wikipedia

    en.wikipedia.org/wiki/Chronic_spontaneous_urticaria

    Angioedema, excruciatingly itchy recurrent wheals, or both can be signs of chronic spontaneous urticaria. [5] Between 40 and 50 percent of CSU patients experience angioedema. [6] However, angioedema is the main symptom reported by about 10% of patients. [7] Usually, urticarial lesions or hives are elevated, erythematous plaques with a defined ...

  6. Pseudoallergy - Wikipedia

    en.wikipedia.org/wiki/Pseudoallergy

    Clinically, pseudoallergy and anaphylaxis are identical. [6] Pseudoallergy symptoms include gastrointestinal symptoms, urticaria, bronchospasm, and angioedema, [7] along with headache, edema, skin flushing, hypotension, and shock. [8]

  7. Hereditary angioedema - Wikipedia

    en.wikipedia.org/wiki/Hereditary_angioedema

    Normal C1 inhibitor level hereditary angioedema is thought to involve various mutations that increased bradykinin activity and cause a decreased threshold for activation of the plasma contact system thus leading to the symptoms of angioedema. [7] Hereditary angioedema with normal C1-inhibitor is a genetically heterogeneous disorder.

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