Document Type
Article
Publication Date
7-29-2021
Abstract
A 14-year-old African American female presented to the emergency department with spontaneous, sudden-onset lip swelling for 1 h. On examination, there was significant water-bag edema of the upper lip extending to the philtrum and premaxilla. Nasopharyngeal laryngoscopy revealed a patent airway without edema. She was initiated on intravenous dexamethasone, famotidine, and diphenhydramine, after which her edema improved but did not resolve. She was subsequently transferred to a local pediatric hospital and upon further testing she was found to have a C1 esterase inhibitor de novo gene mutation. Angioedema causes localized, non-pitting edema of the dermis, subcutaneous and submucosal tissue, and often manifests in the lips, face, mouth, and throat. Signs of laryngeal involvement include change in voice, stridor, dysphagia, and dyspnea. When laryngeal edema is present, it may necessitate definitive airway management and patients should be monitored in the intensive care unit.
Publication Title
International Journal of Emergency Medicine
Recommended Citation
Lesser, Helen and Cohn, Jason E, "Hereditary angioedema." (2021). Otolaryngology (ENT) Resident Research. 81.
https://digitalcommons.pcom.edu/ent_residents/81
PubMed ID
34325646
Comments
This article was published in International Journal of Emergency Medicine, Volume 14, Issue 1, page 43.
The published version is available at https://doi.org/10.1186/s12245-021-00364-7.
Copyright © 2021 The Authors. CC BY 4.0.