Mucoepidermoid carcinoma

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(Redirected from Mucoepidermoid tumor)

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Mucoepidermoid carcinoma
Micrograph of mucoepidermoid carcinoma
Synonyms
Pronounce N/A
Specialty N/A
Symptoms Lump in the salivary gland, pain, difficulty swallowing
Complications Metastasis, nerve damage
Onset
Duration
Types Low-grade, intermediate-grade, high-grade
Causes
Risks Radiation exposure, genetic predisposition
Diagnosis Biopsy, imaging studies
Differential diagnosis Adenoid cystic carcinoma, pleomorphic adenoma
Prevention
Treatment Surgery, radiation therapy, chemotherapy
Medication
Prognosis Depends on grade and stage
Frequency Most common salivary gland malignancy
Deaths N/A


File:Mucoepidermoid carcinoma (2) HE stain.jpg
Mucoepidermoid carcinoma with H&E stain
File:Mucoepidermoid carcinoma (3) HE stain.jpg
Mucoepidermoid carcinoma with H&E stain
File:Mucoepidermoid carcinoma (1) AB-PAS stain.jpg
Mucoepidermoid carcinoma with AB-PAS stain
File:Relative incidence of parotid tumors.png
Relative incidence of parotid tumors
File:Relative incidence of submandibular tumors.png
Relative incidence of submandibular tumors

Mucoepidermoid carcinoma (MEC) is a type of cancer that originates from the salivary glands. It is the most common type of malignancy found in the salivary glands.

Epidemiology[edit]

MEC is most commonly found in adults between the ages of 30 and 50, but it can also occur in children. It is slightly more common in women than in men.

Pathophysiology[edit]

MEC arises from the exocrine glands, which are glands that secrete substances onto an epithelial surface by way of a duct. The tumor is composed of a mixture of cell types, including mucous-secreting cells and squamous cells.

Clinical Presentation[edit]

Patients with MEC often present with a painless mass in the parotid gland, which is the largest of the salivary glands. Other symptoms can include facial nerve paralysis, pain, and skin involvement.

Diagnosis[edit]

The diagnosis of MEC is typically made through a combination of physical examination, imaging studies, and biopsy. Histopathology is used to confirm the diagnosis and to determine the grade of the tumor.

Treatment[edit]

The primary treatment for MEC is surgical removal of the tumor. Radiation therapy may also be used, particularly in cases where the tumor is high-grade or if it has spread to the lymph nodes.

Prognosis[edit]

The prognosis for MEC varies depending on the grade of the tumor and the extent of disease at the time of diagnosis. Low-grade tumors have a good prognosis, with a 5-year survival rate of over 90%. High-grade tumors have a poorer prognosis, with a 5-year survival rate of less than 50%.

See Also[edit]

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