Abstract

Objective: Granulomatosis with polyangiitis (GPA) is a rare autoimmune disease with frequent upper respiratory tract involvement. Early diagnosis is crucial for early initiation of effective treatment, which improves outcome. Imaging plays an important role for confirming clinically suspected cases. The aim of our study is to reveal the frequencies of imaging findings previously defined as suggestive for GPA (i.e. osseous erosions or destructions, neoosteogenesis, subglottic stenosis) and to investigate frequency and characteristics of previously under-recognized nasopharyngeal involvement in GPA.
 Materials and Methods: We retrospectively examined paranasal, nasopharynx/neck, temporal CTs (n=51) and MRIs (n=14) of 48 patients with GPA. The evaluated imaging findings include mucosal ulcerations in nasal cavity, sinonasal and temporal opacifications/inflammatory signal changes, presence and locations of osseous erosions and neoosteogenesis, periantral soft tissue infiltration, septal perforation, presence and characteristics of nasopharyngeal involvement, and subglottic stenosis. Descriptive statistics were presented as mean ± SD; categorical variables were presented as count and percentage.
 Results: Forty patients (87%) had sinonasal and fourteen (29%) patients had tympanic cavity±mastoid opacifications. Three patients (23%) had signal and diffusion characteristics suggesting a sinonasal granulomatous inflammation. Mucosal ulcerations were detected in 32% of patients. Osseous erosions/destruction (40%) was common in disease onset and frequently affected mid-line sinonasal structures. Neoosteogenesis of paranasal sinuses (21%) was more common in follow-up studies and invariably affected maxillary sinuses. Septal perforation (6%), periantral infiltration (4%) and subglottic stenosis (10%) were relatively infrequent findings. Nasopharyngeal involvement (23%) was not infrequent; predominantly presented with wall thickening, ulcerations, low T2-weigted signal changes and restricted diffusion in MRI.
 Conclusion: Sinonasal osseous erosion/destruction is a relatively common and highly suggestive finding especially when co-existent with nasal mucosal ulcerations, neoosteogenesis and nasopharyngeal thickening in a suspected case. Nasopharyngeal involvement is not infrequent and imaging could overlap with other entities such as nasopharyngeal cancer, lymphoma or sarcoma.

Highlights

  • The aim of our study was to reveal the relative frequencies of more specific imaging findings and to investigate the prevalence and imaging characteristics of previously under-recognized nasopharyngeal involvement in Granulomatosis with polyangiitis (GPA)

  • Most of the imaging features of GPA overlap with those of other diseases; familiarity with more specific finding is important to suspect the diagnosis. In this relatively large cohort, we aimed to reveal frequencies of imaging findings previously defined as suggestive for GPA and to investigate the radiologic findings of previously under-recognized nasopharyngeal involvement

  • Lohrmann et al found that mucosal thickening is a frequent finding in both nasal cavity and paranasal sinuses with the ratios of 61% and 75%, respectively [11]

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Summary

Introduction

The CT imaging characteristics of sinonasal involvement are well-described and involve mucosal thickening, osseous erosions or destructions and neoosteogenesis [5]. The aim of our study was to reveal the relative frequencies of more specific imaging findings (i.e., osseous erosions or destructions, neoosteogenesis, subglottic stenosis) and to investigate the prevalence and imaging characteristics of previously under-recognized nasopharyngeal involvement in GPA. Bulut scans were as follows; 1-opacifications/inflammatory signal changes in the nasal cavity and/or paranasal sinuses, 2- mucosal ulcerations and/or septations in the nasal cavity, 3-presence and location of partial or complete osseous erosions, septal perforation 4- presence and location of paranasal neo-osteogenesis, 5-periantral soft tissue infiltration, 6-opacifications/signal changes in the mastoid cells and/or tympanic cavity, 8- mastoid sclerosis, 9- nasopharyngeal thickening and/or ulceration, 10-parapharyngeal infiltration, 11-signal, enhancement and diffusion characteristics of nasopharyngeal involvement, 12-subglottic stenosis, 13-dural thickening and/or calcification.

Results
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