Journal of Postgraduate Medicine
 Open access journal indexed with Index Medicus & ISI's SCI  
Users online: 3625  
Home | Subscribe | Feedback | Login 
About Latest Articles Back-Issues Articlesmenu-bullet Search Instructions Online Submission Subscribe Etcetera Contact
 ::  Similar in PUBMED
 ::  Search Pubmed for
 ::  Search in Google Scholar for
 ::  Article in PDF (596 KB)
 ::  Citation Manager
 ::  Access Statistics
 ::  Reader Comments
 ::  Email Alert *
 ::  Add to My List *
* Registration required (free) 

  IN THIS Article
 ::  References
 ::  Article Figures

 Article Access Statistics
    PDF Downloaded9    
    Comments [Add]    

Recommend this journal


  Table of Contents     
Year : 2023  |  Volume : 69  |  Issue : 1  |  Page : 59-60

An unusual presentation of seronegative Sjögren's syndrome

Department of Medicine, Atal Bihari Vajpayee Institute of Medical Sciences and Dr. Ram Manohar Lohia Hospital, New Delhi, India

Date of Submission01-Mar-2022
Date of Decision01-Apr-2022
Date of Acceptance07-Apr-2022
Date of Web Publication23-Dec-2022

Correspondence Address:
M Chaudhari
Department of Medicine, Atal Bihari Vajpayee Institute of Medical Sciences and Dr. Ram Manohar Lohia Hospital, New Delhi
Login to access the Email id

Source of Support: None, Conflict of Interest: None

DOI: 10.4103/jpgm.jpgm_212_22

Rights and Permissions

How to cite this article:
Chaudhari M, Agarwal N. An unusual presentation of seronegative Sjögren's syndrome. J Postgrad Med 2023;69:59-60

How to cite this URL:
Chaudhari M, Agarwal N. An unusual presentation of seronegative Sjögren's syndrome. J Postgrad Med [serial online] 2023 [cited 2023 Jun 3];69:59-60. Available from:

A 50-year-old female presented to the outpatient department with a history of gradually progressive painless swelling over both upper eyelids for the past two and half years. The patient also had a history of dryness of the mouth and difficulty in swallowing food for the past four months. There was no history of pain or redness of eyes or oral mucosa, fever, weight loss, joint pains, cough, shortness of breath, drug intake, and diabetes mellitus. She had stable vitals and systemic examination was unremarkable. On local examination, it was found that there were swellings involving the lateral part of both upper eyelids over the area of lacrimal glands as shown in [Figure 1]. These swellings were 2 x 1 cm in size, firm, non-fluctuating, and non-tender. There was no enlargement of the parotid and submandibular glands. Because of suspicion of keratoconjunctivitis sicca, the Schirmer test was performed. It showed 4 mm moistened area in 5 minutes thus positive for dry eyes.[1] Fluorescein staining of the cornea was performed. The cornea was divided into the superior, central, and inferior areas. Each area was given a score of 0 (for no staining) to 3 (for continuous epithelial defect), the maximum score being 9. The right and left cornea had scores of 6 and 3, respectively.[2] The patient's HBsAg, anti-hepatitis C, and HIV antibody titers were normal. HbA1c, lipid, and thyroid profiles were unremarkable. Erythrocyte sedimentation rate and C-reactive protein were elevated suggestive of inflammatory etiology. Anti-nuclear antibodies (ANA), rheumatoid factor (RF), and anti-cyclic citrullinated peptides were negative. Autoimmune markers for Sjögren's syndrome anti-Ro (SS-A) and anti-La (SS-B) were negative. ANA was performed using an indirect immunofluorescence assay (IIF) and the rest of the autoimmune markers were measured using enzyme-linked immunosorbent assays (ELISA).
Figure 1: Bilateral lacrimal gland enlargement

Click here to view

As anti-Ro and anti-La antibodies turned out to be negative, the possibility of IgG4-related disorder was entertained and serum IgG4 levels were sent; which also turned out to be normal (less than 140 mg/dL). Computed tomography scan was suggestive of well-defined homogeneously enhancing symmetrical lesions in the superolateral aspect of bilateral orbits, likely of lacrimal gland origin, and the parotid glands were unremarkable. Biopsy was suggestive of highly cellular benign lymphoepithelial lesions involving the lacrimal gland as shown in [Figure 2]; there was no evidence of spindle-shaped fibroblasts of IgG4-positive plasma cells. Biopsy findings were strongly in favor of Sjögren's syndrome. The patient was started on prednisolone and artificial tears. She improved within a few weeks of follow-up.
Figure 2: (a and b) FNAB of lacrimal gland showing large number of lympoepithelial cells with epitheloid cells suggestive of Sjögren's syndrome. (HE stain, magn. 200x)

Click here to view

Although keratoconjunctivitis sicca and xerostomia are common features of Sjögren's syndrome, the lacrimal gland enlargement is considered to be unusual. Causes of the lacrimal gland enlargement are broadly divided into two categories: neoplastic (epithelial/lymphoid tumors) and inflammatory (infectious/non-infectious). Infectious etiologies represent acute dacryoadenitis with painful, tender enlargement of glands, and erythema with discharge, which includes mainly viral and bacterial causes. Inflammatory non-infectious etiologies result in subacute to chronic painless enlargement of glands and these include orbital pseudotumor and Mikulicz's disease (as a part of IgG4-related disorder), sarcoidosis, and Sjögren's syndrome.[3],[4] Mikulicz's disease is an IgG4-related disorder characterized by the combination of the bilateral lacrimal gland as well as parotid and submandibular gland enlargement. It has lymphoplasmacytic infiltration with IgG4 positive cells, storiform fibrosis, and obliterative phlebitis on biopsy, while sarcoidosis will have non-necrotizing granulomatous inflammation.[4] Autoimmune antibodies anti-Ro/La are present in 60-80% of primary Sjögren's syndrome cases.[3],[4] Around 15% of cases of primary Sjögren's syndrome are seronegative for anti-Ro/La, ANA, and RF; these are diagnosed based on clinical features and lymphocytic infiltration on biopsy.[5] The present case had unusual characteristics in terms of lacrimal gland enlargement and negative autoimmune markers.

Declaration of patient consent

The authors certify that appropriate patient consent was obtained.

Financial support and sponsorship


Conflicts of interest

There are no conflicts of interest.

 :: References Top

Stevens S. Schirmer's test. Community Eye Health 2011;24:45.  Back to cited text no. 1
Usuba FS, de Medeiros-Ribeiro AC, Novaes P, Aikawa NE, Bonfiglioli K, Santo RM, et al. Dry eye in rheumatoid arthritis patients under TNF-inhibitors: Conjunctival goblet cell as an early ocular biomarker. Sci Rep 2020;10:14054.   Back to cited text no. 2
Patel R, Patel BC. Dacryoadenitis. In: StatPearls. Treasure Island (FL): StatPearls Publishing; 2022. Available from:  Back to cited text no. 3
Baer AN. Diagnosis and classification of Sjögren's syndrome. In: UpToDate, Post, TW (Ed), UpToDate, Waltham, MA, 2022. Available from:  Back to cited text no. 4
Yazisiz V, Aslan B, Erbasan F, Uçar İ, Öğüt TS, Terzioğlu ME. Clinical and serological characteristics of seronegative primary Sjögren's syndrome: A comparative study. Clin Rheumatol 2021;40:221-9.  Back to cited text no. 5


  [Figure 1], [Figure 2]


Print this article  Email this article
Online since 12th February '04
2004 - Journal of Postgraduate Medicine
Official Publication of the Staff Society of the Seth GS Medical College and KEM Hospital, Mumbai, India
Published by Wolters Kluwer - Medknow