These tumours closely resemble thymoma with pseudosarcomatous stroma. However, the epithelial component is described as carcinomatous with variable atypia and mitotic activity. the spindle cell component shows a gradual transition from the epithelial component. Moreover, the spindle cell component is positive for cytokeratins and for EMA. There may be mesenchymal metaplasia with expression of actin, desmin, or neural markers (chromogranin, S-100 or GFAP).
Immunohistochemistry
|
epithelial component |
spindle cell component |
||
cytokeratins |
positive1 |
positive1 |
||
positive1 |
positive1 |
|||
positive1 |
positive1 |
|||
2/41 |
2/41 |
|||
1/4 (minority of cells)1 |
1/4 (minority of cells)1 |
|||
1/4 (minority of cells)1 |
1/4 (minority of cells)1 |
|||
1/4 (minority of cells)1 |
1/4 (minority of cells)1 |
|||
1/4 (minority of cells)1 |
1/4 (minority of cells)1 |
|||
Differential diagnosis
Prognosis
One of four patients developed a recurrence.
References
2Shimosato Y et al. Tumors of the mediastinum. In: Rosai J, Sobin LH, eds. Atlas of Tumor Pathology. 3rd Edn. Armed Forces Institute of Pathology 1997;93-115