Myoepithelioma of parotid: an unusual clinical entity with immunohistochemistry
Sachin Sharma, Jyoti Kashyap, Ankur Sharma
Abstract
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Sachin Sharma, Jyoti Kashyap, Ankur Sharma
Abstract
Open-access reader
Myoepithelioma was recognized as a histological distinct entity by World Health organization (WHO) in 1991. Only 1% of all salivary gland neoplasms are myoepithelioma. Most commonly affect parotid in approximately 40%. Myoepithelioma is usually a benign tumour arising from neoplastic myoepithelial cells which lack ductal differentiation. The salivary gland tumors in which the ducts comprise less than 5% of the section are classified as myoepitheliomas and in contrast to pleomorphic adenoma myoepithelioma does not show chondroid or osteoid formation. Immunohistochemical analysis can aid in the diagnosis with immunoreactivity to S-100, P63, Calponin, GFAP and myogenic markers. In this report we present a case of myoepithelioma in retroauricular region.
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Myoepithelioma was recognized as a histological distinct entity by World Health organization (WHO) in 1991. Only 1% of all salivary gland neoplasms are myoepithelioma. Most commonly affect parotid in approximately 40%. Myoepithelioma is usually a benign tumour arising from neoplastic myoepithelial cells which lack ductal differentiation. The salivary gland tumors in which the ducts comprise less than 5% of the section are classified as myoepitheliomas and in contrast to pleomorphic adenoma myoepithelioma does not show chondroid or osteoid formation. Immunohistochemical analysis can aid in the diagnosis with immunoreactivity to S-100, P63, Calponin, GFAP and myogenic markers. In this report we present a case of myoepithelioma in retroauricular region.
Key concepts: Myoepithelioma, Myoepithelial cell, Calponin, Pleomorphic adenoma, Medicine, Pathology, Immunohistochemistry, Parotid gland