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Case Report | Volume 11 Issue 10 (October, 2025) | Pages 291 - 294
Oncocytic Variant of Mucoepidermoid Carcinoma Parotid – A Surgical Case Report
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1
Associate Professor, Dept. of Otorhinolaryngology – Head and Neck Surgery, Saraswathi Institute of Medical Sciences (SIMS) Anwarpur ,Hapur, U.P
2
Assistant Professor, Dept. of Anaesthesia and Critical Care, Government Institute of Medical Sciences ( GIMS ) Greater Noida , U.P
3
Assistant Professor, Dept. of Otorhinolaryngology – Head and Neck Surgery Saraswathi Institute of Medical Sciences (SIMS) Anwarpur ,Hapur, U.P.
4
Senior Resident , Dept. of Otorhinolaryngology – Head and Neck Surgery, Indraprastha Apollo Hospital ( IAH ), New Delhi
5
MBBS Student Saraswathi Institute of Medical Sciences (SIMS) Anwarpur ,Hapur, U.P
Under a Creative Commons license
Open Access
Received
Sept. 2, 2025
Revised
Sept. 16, 2025
Accepted
Sept. 29, 2025
Published
Oct. 14, 2025
Abstract
Background: Oncocytic changes in salivary glands can be seen in Warthins, Pleomorphic adenoma, and Acinic cell carcinoma. Mucoepidermoid carcinoma rarely show significant oncocytic changes and oncocytic variant of mucoepidermoid carcinoma is very rare. In my case preoperative diagnosis on FNAC was mucoepidermoid carcinoma. Only on histology tumour showed predominantly oncocytic cells in a background of goblet and mucus secreting cells. Mucoepidermoid carcinoma (MEC) formed by three principle cell types which are mucinous, squamous and intermediate cells. MEC can also be classified into high grade (fast growing) and low grade (slow growing) salivary gland tumour. MEC is the most common type of salivary gland cancer most commonly seen in parotid and uncommon in submandibular or minor salivary glands. They are usually low grade but they can also be intermediate or high grade. Low grade tumours rarely metastasise. MEC accounts for 50 percent of all parotid malignancies. Female preponderance with mean 45 years presentation is most commonly seen. Clinical behaviour of mucoepidermoid carcinoma ranges from indolent to rapid with metastatic spread. Oncocytic variant of mucoepidermoid carcinoma is very rare .Here we report a case of 28 year old male with right side parotid swelling since last 2 years.
Keywords
INTRODUCTION
The cytologic diagnosis of Mucoepidermoid carcinoma ( esp the low grade) is challenging, due to overlapping cytomorphology with benign lesions . High grade neoplasm on the other hand can be easily recognized as malignant based on tumour necrosis, nuclear pleomorphism and high mitotic activity. Oncocytic variant of mucoepidermoid carcinoma (OMEC) is rare. To label it as OMEC, tumour must be composed of 50 percent or more of oncocytic cells1. A diffuse nuclear staining from p63 immunostaining is done for diagnosis of OMEC. FISH detection of MAMC2 gene translocation detection is of great value in its diagnosis2.
CASE DESCRIPTION
A 28 year old male presented with swelling in right parotid for last 2 years. The swelling was painless and of the size of a pea and gradually increased to the size of an orange .There is no past history of DM, HTN, and any other co morbidities. On examination 2*2 cm oral subcutaneous swelling in right parotid region is present, firm in consistency and mobile (IMAGE 1). There is no local rise of temperature and no tenderness. No scar mark is present. No cervical lymphadenopathy is present. Skin above the swelling is smooth.
RESULTS
The specimen was sent for histopathological examination which established the diagnosis (IMAGE 4). Polygonal oncocytes seen in a densely fibrous stroma. Intermediate cells with interspersed mucocytes seen along with granular cytoplasm and distinct cell membrane borders. The patient was in regular follow up for 6 months with proper healing and no sign of recurrence.
DISCUSSION
Mucoepidermoid carcinoma is the most common type of salivary gland cancers. It accounts for 5 to 10 percent of all salivary gland neoplasms3 .It is mostly seen in parotid. FNAC accessibility is feasible for this reason. MEC is formed by 3 principal cell types - squamous, mucinous, and intermediate. MEC has other morphological variants OMEC, Sebaceous cells, Spindle cells, Goblet cells and Clear cells. Oncocytic variant is very rare. To label it as oncocytic, tumour should consist of > 50 percent oncocytic cells. MEC classified into low grade and high grade4. High grade can still be differentiated based on clinical features like facial nerve palsy, deep fixation, lymphadenopathy and cytological findings like tumour necrosis and nuclear pleomorphism5. On the contrary low grade MEC is difficult to diagnose because of overlapping features and clinical similarities with other parotid neoplasm6. Differential diagnosis of OMEC are oncocytoma and oncocytic carcinoma. Oncocytomas are usually seen in elderly. Mostly in females in 6th and 7th decade7. It affects parotid gland in 80 percent cases8. They are benign neoplasm with well circumscribed mass, composed of layers of oncocytes with no mitotic figures9. They are described as large round cells with abundant granular cytoplasm10. They are slow glowing tumours. Oncocytic carcinoma are very rare, mostly seen in males and affects parotid and submandibular gland. They are high grade tumours seen after radiotherapy. On Histopathology they show adenocarcinoma type features, infiltrative growth, mucus production, perineural invasion, atypia and mitotic figures11. OMEC on other hand is low to intermediate grade malignancy . They consist of predominantly oncocytes with small number of mucocytes. Diagnosis of OMEC is very challenging. p63 immunostaining and MAML2 gene translocation useful tool for its diagnosis12.
CONCLUSION
OMEC is a rare tumour and they are mostly seen in parotids with female’s preponderance. High degree of suspicion is required for its diagnosis with stress on histopathological findings and immunostaining. Treatment is surgical excision with follow up for recurrence and radiotherapy in case of perineural invasion.
REFERENCES
1. Hicks J, Flaitz C. Mucoepidermoid carcinoma of salivary glands in children and adolescents: Assessment of proliferation markers. Oral Oncol. 2000;36:454–60. doi: 10.1016/s1368-8375(00)0003-6 2. Luna MA, Batsakis JG, El – Naggar AK. Salivary gland tumors in children. Ann Otol Rhinol Laryngol. 1991;100:869–71. doi: 10.1177/000348949110001016. 3. Neville BW, Damm D, Allen CM, Bouquot JE. Salivary gland pathology. In: Neville BW, editor. Oral and Maxillofacial Pathology. Missouri: Saunders; 2009. pp. 495–7 4. Castro EB, Huvos AG, Strong EW, Foote FW., Jr Tumors of the major salivary glands in children. Cancer. 1972;29:312–7. doi: 10.1002/1097-0142(197202)29:2<312::aid-cncr2820290207>3.0.co;2-#. 5. Rajendran R. Tumors of the salivary gland. In: Rajendran R, Sivapathasundharam B, editors. Shafer's Textbook of Oral Pathology. India: Elsevier; 2009. pp. 219–53. 6. Foote FW, Jr, Frazell EL. Tumors of the major salivary glands. Cancer. 1953;6:1065–133. doi: 10.1002/1097-0142(195311)6:6<1065::aid-cncr2820060602>3.0.co;2-0. 7. Jakobsson PA, Blanck C, Eneroth CM. Mucoepidermoid carcinoma of the parotid gland. Cancer. 1968;22:111–24. doi: 10.1002/1097-0142(196807)22:1<111::aid-cncr2820220114>3.0.co;2-j. 8. Fonseca I, Martins AG, Soares J. Epithelial salivary gland tumors of children and adolescents in southern Portugal. A clinicopathologic study of twenty-four cases. Oral Surg Oral Med Oral Pathol. 1991;72:696–701. doi: 10.1016/0030-4220(91)90014-4. 9. Yu GY, Li ZL, Ma DQ, Zhang Y. Diagnosis and treatment of epithelial salivary gland tumours in children and adolescents. Br J Oral Maxillofac Surg. 2002;40:389–92. 10. Moshy J, Owibomaingere S, Mwakyoma H. Intraoral minor salivary glands neoplasms; the pattern and management. Prof Med J. 2010;17:483–9. 11. Eveson JW, Cawson RA. Tumours of the minor (oropharyngeal) salivary glands: A demographic study of 336 cases. J Oral Pathol. 1985;14:500–9. doi: 10.1111/j.1600-0714.1985.tb00522.x. 12. Waldron CA, El - Mofty SK, Gnepp DR. Tumors of the intraoral minor salivary glands: A demographic and histologic study of 426 cases. Oral Surg Oral Med Oral Pathol. 1988;66:323–33. doi: 10.1016/0030-4220(88)90240-x.
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