Salivary Gland Tumors: Types, Symptoms, and Diagnosis

Salivary Gland Tumors: Types, Symptoms, and Diagnosis

Salivary gland tumors are growths that form in the glands that produce saliva. Most occur in the parotid gland near the ear. About 75 to 80 percent are benign, but every lump needs evaluation to rule out cancer.

7 min readMedically reviewed contentLast updated April 28, 2026

Key Takeaways

  • Most salivary gland tumors are benign, but only biopsy and microscopic review can confirm whether a growth is cancerous.
  • The parotid gland (in front of the ear) is the most common site, followed by the submandibular gland under the jaw.
  • A painless lump is the most common early sign. Pain, facial weakness, or rapid growth raise concern for malignancy.
  • Fine-needle aspiration (FNA) cytology is the standard first diagnostic test, often paired with MRI or ultrasound imaging.
  • Surgery is the primary treatment for most tumors. Radiation may be added for malignant or high-risk cases.
  • An oral pathologist reviews tissue under the microscope to classify the tumor and guide treatment decisions.

What Are Salivary Gland Tumors?

Salivary gland tumors are abnormal growths that develop in the glands producing saliva, including the parotid, submandibular, sublingual, and minor glands lining the mouth and throat.

There are three pairs of major salivary glands. The parotid glands sit in front of each ear. The submandibular glands lie under the jaw. The sublingual glands rest beneath the tongue. Hundreds of minor salivary glands also line the lips, cheeks, palate, and upper airway.

Salivary gland tumors are uncommon overall. They make up roughly 3 to 6 percent of head and neck tumors.[8] The parotid gland is the most frequent site, but the proportion of malignant tumors rises in smaller glands. Tumors in the sublingual or minor glands carry a higher cancer risk than those in the parotid.[8]

More than 20 distinct tumor types are recognized. Pleomorphic adenoma is the most common benign type. Mucoepidermoid carcinoma is the most common malignant type.[2] Children can develop salivary gland tumors as well, though much less often than adults.[5][9]

Causes and Risk Factors

The exact cause of most salivary gland tumors is unknown. Research points to a mix of genetic changes, environmental exposures, and prior radiation as the main contributors.

Genetic Changes

Many salivary gland tumors carry specific gene rearrangements that drive tumor growth. A 2024 systematic review identified recurring fusions such as MYB-NFIB in adenoid cystic carcinoma, MAML2 rearrangements in mucoepidermoid carcinoma, and PLAG1 or HMGA2 alterations in pleomorphic adenoma.[2] These molecular fingerprints help pathologists classify tumors accurately and inform prognosis.

Prior Radiation Exposure

Radiation therapy to the head and neck, especially in childhood, increases the long-term risk of salivary gland tumors. The risk applies to both benign and malignant types and may surface decades after treatment.

Other Risk Factors

Age is the strongest demographic factor. Most adult cases occur after age 50. Smoking is linked to Warthin tumor, a benign parotid lesion. Workplace exposures to silica dust, nickel, and certain rubber-industry chemicals have been associated with higher risk in some studies, though the evidence is limited.[8]

Symptoms and Diagnosis

The most common symptom is a painless lump near the ear, jaw, or inside the mouth. Pain, numbness, facial weakness, or rapid growth suggest the tumor may be malignant.

Benign tumors often grow slowly over months or years. Patients may notice a small, firm, mobile bump that does not hurt. Malignant tumors are more likely to grow quickly, feel fixed to surrounding tissue, cause pain, or lead to weakness on one side of the face when the parotid gland is involved.[1] Skin changes, ulceration, or trouble swallowing are late warning signs.

Diagnosis usually starts with a physical exam and imaging. Ultrasound is often the first imaging test. MRI gives detailed soft-tissue views and is preferred for deeper or larger lesions. CT scans help when bone involvement is suspected.[1]

Fine-needle aspiration (FNA) cytology is the standard sampling technique. A thin needle removes cells from the lump for microscopic review. FNA is safe and accurate in most cases, but salivary gland cytology is technically demanding and certain tumor types overlap, leading to occasional misclassification.[4] When FNA results are uncertain, surgical biopsy or excision provides definitive tissue diagnosis.

  • Painless lump near the ear, jaw, or inside the mouth
  • Persistent swelling that does not resolve over several weeks
  • Pain or numbness in the face or jaw area
  • Weakness or drooping on one side of the face
  • Difficulty swallowing or opening the mouth fully
  • A growth that bleeds or ulcerates

Treatment Options

Surgery to remove the tumor is the primary treatment for nearly all salivary gland tumors. Radiation, and sometimes chemotherapy, may be added for malignant or aggressive cases.

Surgical Removal

For parotid tumors, the surgeon typically performs a partial or total parotidectomy while protecting the facial nerve, which runs through the gland. Submandibular and sublingual tumors are removed by excising the entire affected gland. Minor salivary gland tumors are removed with a margin of surrounding tissue.

Complete removal with clear margins is the goal. Incomplete removal of pleomorphic adenoma, the most common benign tumor, is associated with recurrence and a small risk of malignant transformation over time.

Radiation Therapy

Radiation may follow surgery for high-grade malignancies, large tumors, positive surgical margins, perineural invasion, or lymph node involvement.[6] Radiation alone is sometimes used when surgery is not possible due to tumor location or patient health. A 2023 systematic review of minor salivary gland cancers in the larynx and trachea reported that combined surgery and radiation produced better local control than surgery alone for advanced cases.[6]

Chemotherapy and Targeted Therapy

Chemotherapy plays a smaller role in salivary gland cancer than in other head and neck cancers. It is used mainly for metastatic disease or when surgery and radiation are not options. Targeted therapies based on tumor genetics are an evolving area. Drugs that target HER2, androgen receptor, or NTRK fusions show promise in selected tumor subtypes.[2]

Recovery and Aftercare

Most patients return to normal eating and speaking within two to four weeks after parotid or submandibular surgery, though full nerve recovery can take longer.

Initial recovery involves swelling, mild pain, and a surgical drain that is usually removed within a few days. Patients can typically resume light activity within a week. Stitches are removed at one to two weeks. Numbness near the incision is common and often improves over months.

Facial nerve weakness can occur after parotid surgery, especially with large or deep tumors. Most weakness is temporary and resolves within six months. Permanent weakness is uncommon when the nerve is preserved during surgery. Frey syndrome, in which sweating occurs on the cheek during eating, develops in some parotidectomy patients and can be managed with topical treatments or injections.

Follow-up after malignant tumors typically includes physical exams every three to six months for the first two years, then less frequently. Imaging is added based on tumor type and risk. Patients with adenoid cystic carcinoma need long-term surveillance because recurrence can occur many years after initial treatment.

Cost Factors

Costs for diagnosis and treatment of salivary gland tumors vary widely based on tumor type, location, and the procedures involved. In many cases, total costs span from a few thousand to tens of thousands of dollars.

Diagnostic costs typically include imaging (ultrasound, MRI, or CT), fine-needle aspiration, and pathology review. Imaging alone often runs from a few hundred to several thousand dollars depending on modality and facility. Surgical costs depend on whether the procedure is outpatient or inpatient, the gland involved, and whether nerve monitoring is used. Radiation therapy adds further cost when needed.

Insurance generally covers medically necessary diagnosis and treatment, including surgery, pathology, imaging, and radiation. Coverage details vary by plan. Patients should confirm in-network status for the surgeon, hospital, and pathology lab. Hospitals and academic centers often have financial counselors who can outline payment plans or financial assistance.

Costs vary by location, provider, and case complexity. Getting a written estimate before treatment helps avoid surprises.

Specialist vs. General Dentist for Salivary Gland Tumors

Any persistent lump in or around the mouth, jaw, or neck should be evaluated by a specialist. General dentists often spot these growths first, but diagnosis and treatment require specialized expertise.

An oral pathologist reviews tissue samples under the microscope to identify the specific tumor type. This step is critical because more than 20 salivary gland tumor types exist, and treatment differs sharply between them.[2][7] Immunohistochemical and molecular testing are often needed to reach a precise diagnosis.[7]

Treatment is performed by a head and neck surgeon, oral and maxillofacial surgeon, or otolaryngologist with experience in salivary gland surgery. Radiation oncology and medical oncology may be involved in malignant cases. A coordinated team approach produces the best outcomes for complex tumors. You can learn more about the role of these clinicians on the oral-pathology page.

Find an Oral Pathologist Near You

If your dentist or doctor has identified a lump in or around your salivary glands, an oral pathologist can help determine whether it is benign or malignant. Use our directory to find a board-certified oral pathologist in your area for accurate diagnosis and clear next steps.

Search Oral Pathologists in Your Area

Frequently Asked Questions

Are salivary gland tumors usually cancerous?

No. Most salivary gland tumors are benign, especially those in the parotid gland. The proportion of malignant tumors is higher in the smaller submandibular, sublingual, and minor glands.[8] Only biopsy and microscopic evaluation can confirm whether a specific tumor is benign or malignant.

What does a salivary gland tumor feel like?

Most patients first notice a painless, firm lump near the ear, under the jaw, or inside the mouth. Benign tumors are often slow-growing and movable. Pain, rapid growth, fixation to nearby tissue, or facial weakness are warning signs that the tumor may be malignant.[1]

How is a salivary gland tumor diagnosed?

Diagnosis usually combines a physical exam, imaging (ultrasound, MRI, or CT), and a tissue sample. Fine-needle aspiration is the standard sampling method, but salivary gland cytology has well-known pitfalls and may need confirmation by surgical biopsy.[4] An oral pathologist reviews the cells or tissue to determine the tumor type.

Can salivary gland tumors come back after surgery?

Yes, recurrence is possible, particularly with pleomorphic adenoma if the tumor is not fully removed. Some malignant tumors, such as adenoid cystic carcinoma, can recur many years after initial treatment, which is why long-term follow-up matters. Recurrence rates vary by tumor type and surgical margins.

Do children get salivary gland tumors?

Salivary gland tumors are uncommon in children but do occur. A 2023 international study found that mucoepidermoid carcinoma was the most frequent malignant type in pediatric patients, while pleomorphic adenoma was the most frequent benign type.[5] A separate systematic review reported generally favorable survival outcomes when these tumors are treated appropriately.

Will I have facial nerve damage after parotid surgery?

Temporary facial weakness occurs in some patients after parotid surgery and usually improves over weeks to months. Permanent weakness is uncommon when the facial nerve is identified and preserved during surgery. The risk is higher with larger tumors, malignant tumors, or repeat surgeries. Results vary by case complexity and surgeon experience.

Sources

  1. 1.American Cancer Society. Signs and Symptoms of Salivary Gland Cancer.
  2. 2.Albalawi E. Genetic Rearrangements in Different Salivary Gland Tumors: A Systematic Review. Cureus. 2024;16(6):e61639.
  3. 3.Bishop JA. Mucin-rich salivary gland tumors. Semin Diagn Pathol. 2024;41(4):165-172.
  4. 4.Saoud C et al. Pitfalls in Salivary Gland Cytology. Acta Cytol. 2024;68(3):194-205.
  5. 5.Quixabeira Oliveira GA et al. Epithelial salivary gland tumors in pediatric patients: An international collaborative study. Int J Pediatr Otorhinolaryngol. 2023;168:111519.
  6. 6.Montenegro C et al. Treatment and outcomes of minor salivary gland cancers of the larynx and trachea: a systematic review. Acta Otorhinolaryngol Ital. 2023;43(6):365-374.
  7. 7.Swid MA et al. Updated Salivary Gland Immunohistochemistry: A Review. Arch Pathol Lab Med. 2023;147(12):1383-1389.
  8. 8.Cunha JLS et al. Salivary Gland Tumors: A Retrospective Study of 164 Cases from a Single Private Practice Service in Mexico and Literature Review. Head Neck Pathol. 2021;15(2):523-531.
  9. 9.Louredo BVR et al. Clinicopathological analysis and survival outcomes of primary salivary gland tumors in pediatric patients: A systematic review. J Oral Pathol Med. 2021;50(5):435-443.
  10. 10.American Academy of Oral and Maxillofacial Pathology.

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