Features of non-Hodgkin’s lymphoma diagnosed in minor salivary gland biopsies from primary Sjögren’s syndrome patients

Author:

Parreau Simon1ORCID,Nocturne Gaétane2,Mariette Xavier2,Burroni Barbara3,Lazure Thierry4,Besson Florent L56,Régent Alexis1,Mouthon Luc1,Terrier Benjamin1,Seror Raphaele2,Le Guern Véronique1

Affiliation:

1. Department of Internal Medicine, Université Paris Descartes, Referral Center for Rare Autoimmune and Systemic Diseases, Hôpital Cochin, Assistance Publique–Hôpitaux de Paris (APHP), Paris

2. Department of Rheumatology, Université Paris-Saclay, FHU CARE (Cancer and Autoimmunity RElationship), INSERM UMR1184, Centre for Immunology of Viral Infections and Autoimmune Diseases, APHP, Hôpital Bicêtre, Le Kremlin-Bicêtre

3. Department of Pathology, Université Paris Descartes, Hôpital Cochin, APHP, Paris

4. Department of Pathology, Université Paris-Saclay, APHP, Hôpital Bicêtre

5. Department of Biophysics, Nuclear Medicine-Molecular Imaging, Université Paris-Saclay, APHP, Hôpital Bicêtre, Le Kremlin-Bicêtre

6. UMR BioMaps, Inserm/CNRS/CEA/Université Paris-Saclay, Orsay, France

Abstract

Abstract Objective To evaluate the contribution of minor salivary gland biopsy (mSGB) histology in diagnosing primary SS (pSS)-associated non-Hodgkin B-cell lymphoma (NHL). Methods pSS patients with mSGB at NHL diagnosis were included. Results Among the 24 patients (92.3% female, mean age 61.3 years) with an mSGB at NHL diagnosis, 13 (54.2%) had mSGB histology–revealed NHL (mSGB+); it was the only site enabling NHL diagnosis in 10/13 (76.9%) patients. Mucosa-associated lymphoid tissue (MALT) lymphoma was found in 23/24 (95.8%) patients; 100% of mSGB+ identified MALT lymphomas. pSS and lymphoma characteristics were comparable for mSGB+ and mSGB− patients. Eight (61.5%) of the 13 mSGB+ patients and all 11 mSGB− patients were treated for lymphoma. Between diagnosis and 1 year of follow-up, the ESSDAI without the NHL item remained stable (7.4 vs 5.0; P = 0.33) for the five untreated patients, while it decreased significantly for the 19 treated patients (15.8 vs 5.1; P = 0.004). Conclusion For pSS patients with suspected NHL, mSGB histology enabled NHL diagnosis in half of them, MALT was found in 95.8% and all mSGB+ were MALT lymphomas, thereby avoiding more invasive biopsy. Our results suggest that mSGB should be obtained at pSS diagnosis and repeated during follow-up when NHL is suspected.

Publisher

Oxford University Press (OUP)

Subject

Pharmacology (medical),Rheumatology

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