# Ectopic Pleomorphic Adenoma: A Case Study and Scoping Review of the Literature

**Authors:** John Caraway, Alex Yang, Sophia Mckenzie, Noah Meltzer, Michael Noller

PMC · DOI: 10.7759/cureus.102785 · Cureus · 2026-02-01

## TL;DR

This paper presents a case of an ectopic pleomorphic adenoma in the glabellar region and reviews literature on similar tumors in the head and neck.

## Contribution

The study provides the first scoping review of ectopic pleomorphic adenomas in the head and neck region.

## Key findings

- Ectopic pleomorphic adenomas typically present as slow-growing, firm, mobile masses in superficial head or neck regions.
- Forty-six case reports and series were analyzed, with most cases occurring in the 2nd to 6th decades of life.
- Surgical excision was the primary treatment, with only one recurrence following malignant transformation.

## Abstract

We present a case of an ectopic pleomorphic adenoma occurring in the glabellar region of an adult patient and perform the first known scoping review of the literature on ectopic pleomorphic adenomas of the head and neck, seeking to summarize their symptomatology, presentation, and treatment. Two independent reviewers performed searches and qualitative synthesis of relevant literature using PubMed, Embase, and Ovid All EBM Review databases. The authors adhered to the Preferred Reporting Items for Systematic Reviews and Meta-Analyses-Scoping Review (PRISMA-ScR) statement. Included studies reported ectopic pleomorphic adenoma originating above the clavicle. Exclusion criteria included tumors as a result of metastasis or of non-salivary gland origin. Forty-six case series and case reports of ectopic pleomorphic adenomas met the inclusion and exclusion criteria, for a total of 48 tumors. Most cases occurred during the 2nd to 6th decades of life with a male:female ratio of 1:1.2. Ectopic pleomorphic adenomas typically presented as a slow-growing, firm, mobile mass on a superficial region of the head or neck. Pain was reported in 19% of cases. All cases were treated with surgical excision, and there was only one recurrence after a malignant transformation.

## Linked entities

- **Diseases:** pleomorphic adenoma (MONDO:0008401)

## Full-text entities

- **Genes:** VIM (vimentin) [NCBI Gene 7431], PIP (prolactin induced protein) [NCBI Gene 5304] {aka BRST-2, GCDFP-15, GCDFP15, GPIP4}, KRT7 (keratin 7) [NCBI Gene 3855] {aka CK7, K2C7, K7, SCL}, CD34 (CD34 molecule) [NCBI Gene 947], TP53 (tumor protein p53) [NCBI Gene 7157] {aka BCC7, BMFS5, LFS1, P53, TRP53}, S100A1 (S100 calcium binding protein A1) [NCBI Gene 6271] {aka S100, S100-alpha, S100A}, MLANA (melan-A) [NCBI Gene 2315] {aka MART-1, MART1}
- **Diseases:** intracranial lesion (MESH:D020765), ectopic pleomorphic adenomas of the head and neck (MESH:D006258), Tumor (MESH:D009369), Pain (MESH:D010146), headache (MESH:D006261), benign neoplasm of the salivary gland (MESH:D012468), adenomas (MESH:D000236), Warthin tumors (MESH:D000235), heteroplasia (MESH:C562735), benign salivary gland lesions (MESH:D012466), benign mixed skin tumors (MESH:D018198), PCC (OMIM:115700), metastasis (MESH:D009362), facial nerve dysfunction (MESH:D005155), epidermal cysts (MESH:D004814), Ectopic (MESH:C566852), blunt trauma (MESH:D014949), Benign salivary gland tumors (MESH:D008949), pleomorphic (MESH:D008228), PAs (MESH:C535377), myoepithelioma (MESH:D009208)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

7 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12956368/full.md

## References

70 references — full list in the complete paper: https://tomesphere.com/paper/PMC12956368/full.md

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Source: https://tomesphere.com/paper/PMC12956368