Squamous cell carcinoma in Sjogren’s syndrome – case report, management and review of literature

Sjogren’s syndrome (SS) is a chronic autoimmune disorder most commonly associated with lymphoproliferative malignancies, while epithelial tumours are rarely encountered. A patient with primary SS developed a persistent swelling on the lateral tongue, initially reported as inflammatory on biopsy and managed conservatively. Persistent symptoms led to re-evaluation, which revealed well-differentiated squamous cell carcinoma (SCC). Surgical management included partial glossectomy with supraomohyoid neck dissection. Recovery was uneventful, followed by referral for adjuvant radiotherapy. This case highlights the diagnostic difficulty of distinguishing inflammatory from malignant lesions in SS, particularly when initial biopsies are benign. The occurrence of SCC in the absence of conventional risk factors suggests a possible role of autoimmune mechanisms or alternative oncogenic pathways. Awareness of this uncommon association is essential, and persistent oral lesions in patients with SS warrant thorough and repeated evaluation.

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Publication Details

Journal
Acta Oto-Laryngologica Case Reports
Published
2025-11-27
DOI
https://doi.org/10.1080/23772484.2025.2593099
Primary Topic
Salivary Gland Disorders and Functions
Type
article
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article

Squamous cell carcinoma in Sjogren’s syndrome – case report, management and review of literature

Bimalka Seneviratne, Devyani Jha, Devanand Jha, Mohamed Nazeef
Acta Oto-Laryngologica Case Reports
Salivary Gland Disorders and Functions
article

Squamous cell carcinoma in Sjogren’s syndrome – case report, management and review of literature

Bimalka Seneviratne, Devyani Jha, Devanand Jha, Mohamed Nazeef
article en

Abstract

Sjogren’s syndrome (SS) is a chronic autoimmune disorder most commonly associated with lymphoproliferative malignancies, while epithelial tumours are rarely encountered. A patient with primary SS developed a persistent swelling on the lateral tongue, initially reported as inflammatory on biopsy and managed conservatively. Persistent symptoms led to re-evaluation, which revealed well-differentiated squamous cell carcinoma (SCC). Surgical management included partial glossectomy with supraomohyoid neck dissection. Recovery was uneventful, followed by referral for adjuvant radiotherapy. This case highlights the diagnostic difficulty of distinguishing inflammatory from malignant lesions in SS, particularly when initial biopsies are benign. The occurrence of SCC in the absence of conventional risk factors suggests a possible role of autoimmune mechanisms or alternative oncogenic pathways. Awareness of this uncommon association is essential, and persistent oral lesions in patients with SS warrant thorough and repeated evaluation.

Acta Oto-Laryngologica Case ReportsVol. 10(1)
Lanka Hospitals (LK), University of Colombo (LK)
Openalex Percentile: Top 54%
Salivary Gland Disorders and Functions
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Squamous cell carcinoma in Sjogren’s syndrome – case report, management and review of literature — Bimalka Seneviratne, Devyani Jha, et al. · Acta Oto-Laryngologica Case Reports (2025) | TGRS Research Map | TGRS