Is a Biopsy Required to Classify Patients with Idiopathic Retroperitoneal Fibrosis as IgG4-RPF or Non-IgG4-RPF?

Author:

Misirci Salim1ORCID,Ekin Ali1ORCID,Coskun Belkis Nihan2ORCID,Yagız Burcu1,Yılmaz Özgür3,Yıldız Abdulmecit4,Dalkılıç Ediz1,Pehlivan Yavuz1

Affiliation:

1. Department of Internal Medicine, Division of Rheumatology, Bursa Uludag University Faculty of Medicine, Nilufer, Turkey

2. Department of Internal Medicine, Division of Rheumatology, Bursa Uludag Universitesi, Bursa, Turkey

3. Department of Internal Medicine, Bursa Uludag University Faculty of Medicine, Nilufer, Turkey

4. Department of Internal Medicine, Division of Nephrology, Bursa Uludag University Faculty of Medicine, Nilufer, Turkey

Abstract

Abstract Objective Our aim was to group cases of idiopathic retroperitoneal fibrosis (IRPF) into those associated with immunoglobulin (Ig) G4-related disease (IgG4-RD) (IgG4-RPF) and those not associated with IgG4-RD (non-IgG4-RPF) and to compare the clinical presentation, laboratory findings, imaging, and treatment methods. Methods A total of 46 patients were included in the study. According to the assessment by two experienced rheumatologists and the IgG4-RPF classification criteria published by the American College of Rheumatology/European League Against Rheumatism (ACR/EULAR) in 2019, 11 patients who were admitted as IgG4-RPF were included in the IgG4-RPF group and 35 patients who were not admitted as IgG4-RPF were included in the non-IgG4-RPF group. The clinical and demographic characteristics, affected sites, laboratory results and treatments were retrospectively evaluated and compared. Results The mean age of our patients was 50.69 (±11.33) in the non-IgG4-RPF group and 55.36 (±7.80) in the IgG4-RPF group and was similar in both groups (p=0.340). The male gender dominated in both groups. Although there was no significant difference between the groups in terms of acute renal failure (p=0.074), this was more frequent in the IgG4-RPF group (81.82%). An increased IgG4 concentration was found in about half (n=6, 54.55%) of the patients in the IgG4-RPF group, while this was present in only 5.71% (n=2) of the patients in the non-IgG4-RPF group (p=0.001). The most commonly used diagnostic imaging modality was computed tomography. Biopsy was performed in almost all patients (n=10, 90.91%) in the IgG4-RPF group and 11 (31.43%) in the non-IgG4-RPF group (p<0.001). Drug treatment alone and drug treatment in combination with interventional treatment were the most commonly used treatment modalities in the non-IgG4-RPF group (n=12, 34.29% for both). In the IgG4-RPF group, the combination of medical and interventional treatment was the most commonly used treatment modality (n=5, 45.45%). No significant difference was found between the two groups in the assessment of treatment success (p>0.05). Conclusion IRPF can present with similar clinical and imaging findings in IgG4-RPF and non-IgG4-RPF groups. Since a similar treatment success can be achieved in both groups with similar therapeutic agents, we believe that a biopsy is not necessary in patients with an uncertain diagnosis of IRPF.

Publisher

Georg Thieme Verlag KG

Reference30 articles.

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