Very painful acute frontal sinusitis revealing granulomatosis with polyangiitis.
Anti-neutrophil cytoplasmic antibodies
Anti-neutrophil cytoplasmic antibody-associated vasculitis
Frontal sinusitis
Granulomatosis with polyangiitis
Histology
Journal
European annals of otorhinolaryngology, head and neck diseases
ISSN: 1879-730X
Titre abrégé: Eur Ann Otorhinolaryngol Head Neck Dis
Pays: France
ID NLM: 101531465
Informations de publication
Date de publication:
Nov 2019
Nov 2019
Historique:
pubmed:
10
8
2019
medline:
5
6
2020
entrez:
10
8
2019
Statut:
ppublish
Résumé
Granulomatosis with polyangiitis (GPA) is a necrotizing vasculitis of small and medium-sized vessels comprising inflammation of the vessel wall and perivascular and extravascular granulomas, frequently presenting in the form of chronic sinusitis. We report the case of a 27-year-old man who presented with very painful acute frontal sinusitis that was managed medically and surgically. The symptoms rapidly recurred despite treatment and CT scan demonstrated diffuse thickening of the sinus mucosa. Anti-proteinase 3 ANCA were positive. Biopsy of a pulmonary nodule confirmed the diagnosis of GPA. The patient was treated with corticosteroids in combination with rituximab, resulting in improvement of the clinical, laboratory and CT signs. In the presence of persistent, acute, localized sinusitis despite appropriate treatment, associated systemic signs and/or the presence of other signs suggestive of GPA, the ENT surgeon must request a targeted work-up. In the absence of treatment, GPA can be fatal within a few months. However, with currently available treatment, remission is obtained in 80% of cases with a 75% 10-year survival rate.
Identifiants
pubmed: 31395462
pii: S1879-7296(19)30098-5
doi: 10.1016/j.anorl.2019.05.008
pii:
doi:
Substances chimiques
Antibodies, Antineutrophil Cytoplasmic
0
Myeloblastin
EC 3.4.21.76
Types de publication
Case Reports
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
509-511Informations de copyright
Copyright © 2019. Published by Elsevier Masson SAS.