Widal, morbus J45.1

Author: Prof. Dr. med. Peter Altmeyer

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Last updated on: 29.10.2020

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Synonym(s)

Analgesic Asthma Syndrome; anaphylaxis and idiosyncrasy; Samter's disease; Widal-Lermoyez Syndrome

History
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Widal, Abramin and Lermoyez, 1922

Definition
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Clinical syndrome with the following triad (velvet triad):

However, this clinical entity is not limited to ASA. It is also observed in the use of other non-steroidal anti-inflammatory drugs. Patients with Widal's syndrome have a significantly increased tendency to relapse with standard sinusitis therapy.

Occurrence/Epidemiology
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AERD (aspirin-exacerbated respiratory disease) can be detected in about 10% of asthmatics.

Etiopathogenesis
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According to current knowledge, the reaction is not based on an IgE-mediated mechanism. The cause is a dysbalance in the arachidonic acid metabolism (increased leukotriene production), which is increased by the intake of non-steroidal anti-inflammatory drugs or salicylates in the diet.

A mutation in the C444 allele of leukotriene C synthase has been described as a possible cause.

Therapy
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Leave of absence for non-steroidal anti-inflammatory drugs, in particular ASS. Use of leukotriene antagonists. Treatment of nasal polyps.

Internal therapy
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For the treatment of polyposis nasi, "adaptive deactivation" is recommended. For this purpose acetylsalicylic acid is taken permanently according to a defined regimen.

Literature
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  1. May A et al (2000) Family investigation in patients with ASA intolerance and rhinosinusitis. HNO 48: 650-654
  2. Widal MF, Abramin P, Lermoyez J (1922) Anaphylaxis and idiosyncrasy. Press Med 30: 189

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Last updated on: 29.10.2020