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A Diagnostically Challenging Parotid Gland Tumor With Hybrid Features
Steven Hamilton1, Maleeha Saleem1, Mustafa Ali1
1Internal Medicine, Jersey Shore University Medical Center/Saint Francis Medical Center Program, Trenton, USA.
Cureus
|July 12, 2021
Summary
A challenging parotid gland tumor case highlights the importance of accurate histopathological diagnosis. Cellular pleomorphic adenoma with metaplasia can mimic mucoepidermoid carcinoma, impacting treatment decisions.
Area of Science:
- Head and Neck Surgery
- Oncology
- Pathology
Background:
- Salivary gland tumors are rare, with pleomorphic adenoma (benign) and mucoepidermoid carcinoma (malignant) being most common.
- Differentiating these tumors histopathologically can be challenging, impacting patient prognosis and treatment.
- Accurate diagnosis is crucial for appropriate management, potentially avoiding unnecessary aggressive treatments.
Observation:
- A 24-year-old woman presented with a three-year history of left parotid gland swelling, which recently became painful and rapidly enlarged.
- Imaging revealed a complex heterogeneous mass in the superficial left parotid gland.
- Ultrasound-guided biopsy diagnosed a cellular pleomorphic adenoma with mucinous and squamous metaplasia.
Findings:
- Cellular pleomorphic adenoma exhibits increased cellularity and mitotic activity, but is benign.
- Mucinous and squamous metaplasia can mimic mucoepidermoid carcinoma on fine-needle aspiration (FNA), posing a diagnostic challenge.
- Histopathological evaluation of the gross specimen with immunohistochemistry confirmed the diagnosis, differentiating it from mucoepidermoid carcinoma.
Implications:
- Misdiagnosis as mucoepidermoid carcinoma could lead to unnecessary neck dissection and adjuvant therapy, increasing morbidity.
- This case underscores the critical role of adequate tissue biopsy for precise parotid gland tumor diagnosis.
- Optimizing patient care relies on accurate histopathological appraisal to guide treatment strategies and improve outcomes.

