Salivary gland–type carcinoma of the thyroid, also termed intrathyroidal mammary analog secretory carcinoma, has been reported in 12 cases in the English language. In a review of 11 cases, salivary gland–type carcinomas of the thyroid were diagnosed in adult females (9 cases) and males (2 cases) with an average age 61.5 years (range: 36–74 years). These individuals presented with a thyroid mass with two individuals complaining of
shortness of breath and one individual complaining of hoarseness. Their tumors' microscopic
histopathology resembled that described in
the pathology section of mammary secretory carcinoma and consisted of tumor cells that expressed the
NTRK3-ETV6 fusion gene. All cases were treated by
thyroidectomy (removal of the thyroid gland) plus
radiotherapy in 6 cases and/or
chemotherapy in 3 cases. Six of 10 individuals experienced local recurrences (n = 3) or one or more metastases (n = 3) after initial treatment; their tumors had invaded nearby normal thyroid tissues,
trachea, mediastinum, and/or and cartilage and metastasized to the liver, lung, kidney, bone, and/or soft tissues. Salivary gland-type carcinoma of the thyroid appears to be a more aggressive disease than mammary secretory carcinoma or MASCSG.) ==Secretory carcinomas located in other sites==