B-ENT
Case Report

IgG4-Related Pseudotumor in the Sinonasal Cavity: Presentation of a Case and Literature Review

1.

Faculty of Medicine and Health Sciences, University of Antwerp, Wilrijk, Belgium

2.

Department of Otorhinolaryngology and Head & Neck Surgery, Antwerp University Hospital, Edegem, Belgium

3.

Department of Rheumatology, Antwerp University Hospital, Edegem, Belgium

4.

Department of Anatomical Pathology, Antwerp University Hospital, Edegem, Belgium

B-ENT 2022; 18: 121-127
DOI: 10.5152/B-ENT.2022.21466
Read: 161 Downloads: 123 Published: 01 April 2022

Immunoglobulin G4-related disease is an increasingly recognized inflammatory condition that was originally associated with autoimmune pancreatitis. Although the involvement of the salivary glands has been reported, the occurrence of immunoglobulin G4-related disease in the sinonasal cavity is uncommon. We present a case of a 42-year-old woman with immunoglobulin G4-related disease involving the sinonasal cavity. The patient presented with a progressive, non-painful lesion on the left nostril and lateral nasal wall that had been present over the course of 7 months. Moreover, there was an enlarged left submandibular gland and cervical lymphadenopathy. Further examination revealed a septal perforation, extensive inflammation of the sinonasal cavity, and a positive Antineutrophil Cytoplasmic Antibodies (c-ANCA) serology. Although the diagnosis of granulomatosis with polyangiitis was initially suspected, histopathology revealed lymphoplasmacytic infiltrations with an increase of immunoglobulin G4-positive plasma cells, confirming the diagnosis of an immunoglobulin G4-related disease. The patient was treated with oral corticosteroids, after which the symptoms improved. Immunoglobulin G4-related disease originating in the sinonasal cavity is uncommon, and presentation as a nasal pseudotumor is considerably rare.

Cite this article as: Vercauteren L, Van Haesendonck G, Van Offel S, et al. IGG4-related pseudotumor in the sinonasal cavity: presentation of a case and literature review. B-ENT 2022;18(2):121-127.

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