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Resolution of Laryngeal Oedema in a Patient with Acquired C1-Inhibitor Deficiency. A Case Report

Noémi-Anna Bara

Noémi-Anna Bara

Hereditary Angioedema Expertise Centre, Sangeorgiu De MuresMures, Romania
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Bara, Noémi-Anna
 and 
Valentin Nadasan

Valentin Nadasan

George Emil Palade University of Medicine, Pharmacy, Science, and Technology of Targu MuresMures, Romania
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Nadasan, Valentin
  
May 12, 2021
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Article Category: Case Report
Published Online: May 12, 2021
Page range: 136 - 140
Received: Sep 10, 2020
Accepted: Jan 08, 2021
DOI: https://doi.org/10.2478/jccm-2021-0003
Keywords
© 2021 Noémi-Anna Bara, Valentin Nadasan, published by Sciendo
This work is licensed under the Creative Commons Attribution 4.0 International License.

Fig. 1

Abdominal ultrasonography showing splenomegaly in a patient with hereditary angioedema and monoclonal gammopathy of uncertain significance
Abdominal ultrasonography showing splenomegaly in a patient with hereditary angioedema and monoclonal gammopathy of uncertain significance

Fig. 2

Facial oedema apparent at the time of admission to the emergency department
Facial oedema apparent at the time of admission to the emergency department
Language:
English
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4 times per year
Journal Subjects:
Medicine, Clinical Medicine, Internal Medicine, Internal Medicine, other, Surgery, Surgery, other, Anaesthesiology, Emergency Medicine and Intensive-Care Medicine
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