2000•Japanese Journal of Oral & Maxillofacial SurgeryOpen access

Myoepithelioma of the submandibular gland: Report of a case.

Michiko Yoshizawa, Keiko Shibata, Masahito Takada, Kenji Izumi, Susumu Shingaki, 周三 平

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Abstract

A rare case of myoepithelioma originating from the submandibular gland is reported. A 28-yearold woman was referred for treatment of an asymptomatic mass in the left submandibular region. On clinical examination, a 30×15mm hard, mobile, non-tender mass was noted. Ultrasonography and computed tomography demonstrated a large, well-demarcated mass that was not distinct from the submandibular gland. The tumor was removed surgically in March 1998. Histopathologically, the tumor consisted of both spindle-shaped cells and plasmacytoid cells with proliferation of many vessels in the stroma. The neoplastic cells expressed S-100 protein, DF-3, and EMA immunohistochemically. The histopathological diagnosis was myoepithelioma. There was no evidence of recurrence 2 years postoperatively.

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A rare case of myoepithelioma originating from the submandibular gland is reported. A 28-yearold woman was referred for treatment of an asymptomatic mass in the left submandibular region. On clinical examination, a 30×15mm hard, mobile, non-tender mass was noted. Ultrasonography and computed tomography demonstrated a large, well-demarcated mass that was not distinct from the submandibular gland. The tumor was removed surgically in March 1998. Histopathologically, the tumor consisted of both spindle-shaped cells and plasmacytoid cells with proliferation of many vessels in the stroma. The neoplastic cells expressed S-100 protein, DF-3, and EMA immunohistochemically. The histopathological diagnosis was myoepithelioma. There was no evidence of recurrence 2 years postoperatively.

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Available abstract

A rare case of myoepithelioma originating from the submandibular gland is reported. A 28-yearold woman was referred for treatment of an asymptomatic mass in the left submandibular region. On clinical examination, a 30×15mm hard, mobile, non-tender mass was noted. Ultrasonography and computed tomography demonstrated a large, well-demarcated mass that was not distinct from the submandibular gland. The tumor was removed surgically in March 1998. Histopathologically, the tumor consisted of both spindle-shaped cells and plasmacytoid cells with proliferation of many vessels in the stroma. The neoplastic cells expressed S-100 protein, DF-3, and EMA immunohistochemically. The histopathological diagnosis was myoepithelioma. There was no evidence of recurrence 2 years postoperatively.

Key concepts: Myoepithelioma, Submandibular gland, Medicine, Asymptomatic, Stroma, Pathology, Immunohistochemistry, Salivary gland

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