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. Author manuscript; available in PMC: 2016 Oct 1.
Published in final edited form as: J Thorac Oncol. 2015 Oct;10(10):1383–1395. doi: 10.1097/JTO.0000000000000654

Table 3.

Markers considered to be useful for the routine immunohistochemical characterization of otherwise difficult to classify thymomas and thymic carcinomas.3

Marker Cellular and subcellular targets of mediastinal tumors
Cytokeratins Epithelial cells of normal thymus, thymomasa, thymic carcinomas, neuroendocrine tumors, many germ cell tumors, rare sarcomas and dendritic cell tumors; metatases to the mediastinum
Cytokeratin 19 Epithelial cells of normal thymus, thymomasa and thymic carcinomas
Cytokeratin 20 Negative in normal thymus and thymomas. May be positive in rare thymic adenocarcinomas, teratomas or metastases
P63 Nuclei of normal and neoplastic thymic epithelial cells, squamous epithelial cells (e.g. in teratoma, metastasis), primary mediastinal large B-cell lymphoma
P40 Nuclei of normal and neoplastic thymic epithelial cells, squamous epithelial cells (e.g. in teratoma; metastasis)
TdT Immature T cells of normal thymus, >90% of thymomas and neoplastic T cells of T lymphoblastic lymphoma
CD5 Immature and mature T cells of thymus and >90% of thymomas
Neoplastic T cells of many T lymphoblastic lymphomas
Epithelial cells in70% of thymic carcinomasb
CD20 Normal and neoplastic B cells
Epithelial cells in 50% of cases of type A and AB thymoma
CD117 Epithelial cells in 80% of thymic carcinomas
Neoplastic cells in most seminomas
a

Beware of rare cytokeratin-negative thymomas (that typically maintain expression of p63/p40)21;

b

beware of adenocarcinoma metastases to the mediastinum that can be CD5+ as well