A thymic carcinoma resembling the mucoepidermoid tumour of salivary glands.
Only about 20 cases have been reported in the English language literature3. There are no reports of an association with type A or B thymoma.
Patients cover a wide age range, with a mean of about 503. Patients do not have paraneoplastic syndromes3.
Most tumours show a combination of solid and cystic areas3. Mucoid material fills the cysts3. The solid areas appear nodular with fibrous bands.
The tumour consists of a variable mix of epidermoid and mucinous (goblet) cells, along with intermediate cells. Both the squamous and the mucinous component are well-differentiated. Clear cells and oxyphil cells may also be present3. Mucin is often present within the stroma, accompanied by a lymphoplasmacytic infiltrate, foamy macrophages, cholesterol clefts and fibrosis3. There may be focal calcification or ossification3. Non-neoplastic thymic tissue adjacent to the tumour may show cystic change or mucinous metaplasia3. Grading has been applied as for the equivalent salivary gland tumours3.
Cytokeratin |
1/12 |
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1/53 |
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3/53 |
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1/12 |
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0/12, 0/103 |
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0/12 |
|||
0/12 |
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0/12 |
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2/5 (positive in goblet and intermediate cells)3 |
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Tumours with poorly differentiated squamous and mucinous components should be called adenosquamous carcinomas.
High grade adenosquamous carcinoma is more aggressive than is low grade mucoepidermoid carcinoma.
0 Tumours of the Lung, Pleura, Thymus and Heart. WHO Classification of Tumours. IARC Press 2004.
1 J Rosai et al. Histological typing of tumours of the thymus. WHO International histological classification of tumours. Springer-Verlag, second edition, 1999.
This page last revised 6.1.2006.
©SMUHT/PW Bishop