Myoepithelioma
Myoepithelioma is a rare benign tumor that arises from myoepithelial cells, which are a type of cell found in glands such as the salivary glands, sweat glands, and mammary glands. These tumors are most commonly found in the salivary glands, particularly the parotid gland.
Characteristics[edit | edit source]
Myoepitheliomas are characterized by the proliferation of myoepithelial cells without ductal or acinar differentiation. These tumors can vary in appearance, from solid, cystic, to mixed types, and are generally encapsulated, making them distinct from surrounding tissues. Histologically, they can present a variety of cell types, including spindle-shaped, plasmacytoid, and clear cells. The cells are typically arranged in nests, sheets, or trabeculae, and are often surrounded by a fibrous stroma.
Symptoms[edit | edit source]
The symptoms of myoepithelioma depend on the tumor's location but typically include a painless mass. In cases where the tumor grows large enough, it may cause pain or dysfunction of the affected gland. For instance, if the tumor is in the salivary gland, it might lead to difficulties in swallowing or facial nerve palsy.
Diagnosis[edit | edit source]
Diagnosis of myoepithelioma generally involves a combination of imaging studies and histopathological examination. Imaging techniques such as ultrasound, MRI, and CT scans are used to assess the size, shape, and extent of the tumor. Definitive diagnosis is made through a biopsy, where a sample of the tumor is examined under a microscope to identify the characteristic myoepithelial cells.
Treatment[edit | edit source]
The primary treatment for myoepithelioma is surgical removal. Complete excision of the tumor is typically curative, and due to its benign nature, myoepithelioma generally has an excellent prognosis post-surgery. In cases where the tumor is located in a sensitive area, such as near facial nerves, careful surgical techniques are employed to minimize damage to surrounding tissues.
Epidemiology[edit | edit source]
Myoepithelioma is a rare condition, and its exact incidence is not well-documented. It can occur at any age but is most commonly diagnosed in adults. There is no known gender or racial predilection for this tumor.
See Also[edit | edit source]
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Contributors: Prab R. Tumpati, MD