Printer Friendly

Life-Threatening Upper Airway Compression: Quincke's Disease.

Clinical Image

A 34-year-old man presented with sudden onset of dyspnea and throat pain for 2 hours. He had no clinical history of trauma, fever, or allergies and was consuming sea food when he developed the symptoms. There was no history of similar episodes in the past. Examination of the upper airway including the oropharynx revealed an enlarged, swollen, and congested uvula (Figure 1). The remaining physical and indirect laryngeal examination findings were normal and his vitals were stable. He was diagnosed with Quincke's disease was treated with dexamethasone and chlorpheniramine maleate. The patient's symptoms improved in 3 hours and he was discharged on oral cetrizine 10 mg once a day for two days.

In 1882, Quincke first described isolated uvular angioedema. It is a relatively rare presentation of angioedema of the upper airway (1). Several causes have been implicated, such as trauma, hereditary angioedema, inhalation exposure, medication reactions, and infectious causes (2). Although rare, the uvular edema may cause obstructive respiratory distress and require immediate airway care. The treatment consists of intravenous H1 and H2 histamine blockers, corticosteroids, and rarely epinephrine (1, 2). Because of its potent anti-inflammatory properties and long half-life, dexamethasone is considered the medication of choice; however, for epinephrine has proven life-saving for emergency airway care injection. Recurrent attacks are observed in hereditary angioneurotic edema, which is caused by deficiency of the enzyme C1 esterase.

Conclusion

Quincke's disease or uvular edema is an uncommon presentation which can compromise the airway and lead to potentially a life-threatening situation. The treatment includes the administration of antihistamines, corticosteroids, and epinephrine.

ORCID ID of the author: S.S.B. 0000-0003-4859-9588.

Corresponding Author: Satvinder Singh Bakshi e-mail: saty.bakshi@gmail.com

Received: 05.05.2018 * Accepted: 05.06.2018

DOI: 10.5152/eajem.2018.92485

Informed Consent: Written informed consent was obtained from patient who participated in this study.

Peer-review: Externally peer-reviewed.

Conflict of Interest: The authors have no conflict of interest to declare.

Financial Disclosure: The authors declared that this study has received no financial support.

References

(1.) Mattingly G, Rodu B, Alling R. Quincke's disease: Nonhereditary angioneurotic edema of the uvula. Oral Surg Oral Med Oral Pathol. 1993; 75: 292-5. [CrossRef]

(2.) Yigit M, Sogut O, Lisar H, Yigit E. Usefulness of C1 esterase inhibitor protei concentrate in the management of hereditary angioedema of oropharyngeal tissue. Niger J Clin Pract. 2018; 21: 531-3.

Satvinder Singh Bakshi (iD)

Mahatma Gandhi Medical College and Research Institute, Sri Balaji Vidyapeeth; Puducherry, India

Caption: Figure 1. Patient with swollen and erythematous uvula

COPYRIGHT 2018 AVES
No portion of this article can be reproduced without the express written permission from the copyright holder.
Copyright 2018 Gale, Cengage Learning. All rights reserved.

Article Details
Printer friendly Cite/link Email Feedback
Title Annotation:Image of Interest
Author:Bakshi, Satvinder Singh
Publication:Eurasian Journal of Emergency Medicine
Article Type:Clinical report
Date:Dec 1, 2018
Words:419
Previous Article:Metallic Foreign Bodies in the Thoracic Wall in Three Cases.
Next Article:Patient with Anaphylaxis Following Blunt Abdominal Trauma.
Topics:

Terms of use | Privacy policy | Copyright © 2022 Farlex, Inc. | Feedback | For webmasters |