منابع مشابه
Hereditary angio-oedema
Hereditary angio-oedema is caused by a heterozygous deficiency of C1 inhibitor. This inhibitor regulates several inflammatory pathways, and patients with hereditary angio-oedema have intermittent cutaneous or mucosal swellings because of a failure to control local production of bradykinin. Swellings typically evolve in several hours and persist for a few days. In addition to orofacial angio-oed...
متن کاملUrticaria and angio-oedema.
Urticaria and angio-oedema are a symptom complex covering a wide range of clinical disorders. Specific types are now well described, and it appears that many cases of idiopathic chronic urticaria which make up the vast majority of patients referred for assessment are due to intolerance to natural salicylates, preservatives and colouring agents. There is, therefore, an urgent need for legislatio...
متن کاملUrticaria, angio-oedema and anaphylaxis.
laxis are distinct clinical entities caused by transient plasma leakage from small blood vessels. When the affected vessels are superficial the result is a raised, itchy swelling of the skin known as a weal. Involvement of deeper vessels produces tender subcutaneous and submucosal swellings known as angio-oedema. Generalised plasma exudation leading to shock is a feature of anaphylaxis but also...
متن کاملAngio-oedema associated with colistin.
A 50-year-old woman known to have type 1 diabetes mellitus presented with a rare case of angio-oedema associated with colistin use. The angio-oedema was temporally associated with the use and discontinuation of colistin with the reasonable exclusion of important differential diagnoses. Pseudoallergy may be a probable underlying mechanism. However, we cannot exclude the possibility of hereditary...
متن کاملHereditary angio-oedema with mesangiocapillary glomerulonephritis.
A patient with hereditary angio-oedema (HAO) developed mesangiocapillary glomerulonephritis (MCGN) under observation. HAO is characterized by an inherited defect of complement-deficiency of C1 esterase. MCGN is often associated with another complement abnormality which leads to depression of serum C3 and there is some evidence that the complement abnormality precedes the nephritis. The coincide...
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ژورنال
عنوان ژورنال: Journal of the Royal Society of Medicine
سال: 1984
ISSN: 0141-0768,1758-1095
DOI: 10.1177/014107688407701114