These tumours are rare but are the most common type of thymic carcinoma. The frequency is higher in Asia than in the West.
There may be paraneoplastic polymyositis but not myasthenia gravis, unless the carcinoma has arisen by progression from a thymoma, nor red cell aplasia.
The tumour is not encapsulated and lacks fibrous septa. There is often necrosis or haemorrhage. Invasion of lung, pericardium and major vessels is common. Most tumours are Masaoka stage III or IV at the time of presentation.
These tumours consist of epithelial lobules separated by fibrous bands permeated by inflammatory cells. The squamous cells show intercellular bridges and keratinisation. There is definite cytological atypia. Broad bands of fibrohyaline stroma separate the tumour nests. And lymphocytes are mature and admixed with plasma cells.
Cytokeratin |
1/12 |
||
1/12 |
|||
positive0 |
|||
positive0 |
|||
positive0 |
|||
positive alone or in combination in two-thirds of cases0 |
|||
Squamous cell carcinoma metastatic from other sites usually lack the organisation into lobules separated by fibrous bands, as seen in thymic squamous cell carcinoma. Squamous carcinomas of other organs are negative for CD5 and CD700. Nasopharyngeal carcinomas may be positive for CD700.
Thymomas: negative for CD5 (except for some of B3 type) and are infiltrated by immature T-cells.
If associated with a cyst, needs to be differentiated from pseudopapillary growth seen in multilocular thymic cysts.
Metastases occur to lymph nodes, bone, lung, liver and brain. The prognosis, along with that of basaloid carcinoma, is better than for other thymic carcinomas.
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