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ISSN: 2155-9899

Journal of Clinical & Cellular Immunology
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Research Article

Obstructive Sleep Apnea and Lymphocytic Sialadenitis: The Focus isnt Just Sjgrens Syndrome

Ashhad Mahmood1, Jonathan F Lara1# and Elliot D Rosenstein2*
1Department of Pathology, St. Barnabas Medical Center, Livingston, NJ, USA
2Institute for Rheumatic and Autoimmune Diseases, Overlook Medical Center, Summit, NJ, USA
#deceased
Corresponding Author : Elliot D Rosenstein, MD
Institute for Rheumatic & Autoimmune Diseases
Overlook Medical Center, 33 Overlook Road, Summit, NJ, USA
Tel: 908-598-7940
Fax: 908-598-5447
E-mail: [email protected]
Received: September 25, 2015 Accepted: October 28, 2015 Published: October 30, 2015
Citation: Mahmood A, Lara JF, Rosenstein ED (2015) Obstructive Sleep Apnea and Lymphocytic Sialadenitis: The Focus isn’t Just Sjögren’s Syndrome . J Clin Cell Immunol 6:368. doi:10.4172/2155-9899.1000368
Copyright: © 2015 Mahmood A, et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
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Abstract

Objective: We examined the presence of lymphocytic infiltration and measured focus scores in uvular specimens of patients with obstructive sleep apnea (OSA).

Methods: We reviewed the histopathology of 101 uvular specimens obtained from patients with OSA and uvular hypertrophy. A lymphocyte focus score assessment was performed for each case.

Results: Of the 101 cases, 42 (42%) cases had a positive focus score (score ≥ 1). Of those cases with a positive focus score, 22 (52%) had a focus score of 1, 14 (33%) had a focus score of 2, 4 (9%) had a focus score of 3, and 2 (5%) had a focus score of 4. Of the 59 patients (58%) with negative focus scores, 39 (66%) had minor lymphocytic infiltrates; 17 (29%) had features of chronic sialadenitis or extensive fibrosis; 3 (5%) had salivary mucosa without any apparent lymphocytes.

Conclusion: Our findings indicate that patients with OSA may exhibit focal lymphocytic sialadenitis (FLS). It remains to be determined whether mucosal changes occur elsewhere in the oral cavity of patients with OSA. If so, the presence of OSA may complicate the histologic evaluation of Sjögren’s syndrome. Further investigations to determine the prevalence of FLS in the uvulae of individuals without history of OSA, the extent of FLS elsewhere within the oral cavity of patients with OSA and the relationship between the local inflammatory reaction and the systemic consequences of OSA are needed.

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