Table 5 Criteria for differential diagnosis of sarcomatoid pleural tumors

From: Sarcomatoid mesothelioma: a clinical–pathologic correlation of 326 cases

 

Sarcomatoid mesothelioma

Sarcomatoid carcinoma

Monophasic synovial sarcoma

Malignant solitary fibrous tumor

Gross distribution, clinical

Pleural-based tumor, confluent, diffusely infiltrating. Very rarely localized. Usually in males of >50 years

Usually more localized deposits, rarely generalized. Frequently peripheral (often apical) lung mass

Any site but usually relatively circumscribed. Rarely more generalized, often in younger age (40–50 years)

Usually fairly localized, in younger age (30–50 years)

Immunohistochemistry

CK+ (usually)

CK+, other carcinoma-related markers may also be positive

CK+ (focal) CD99+ BCL2+ (rarely calretinin+)

CK, C34+ Bcl2+ CD99+

Other

Electron microscopy rarely contributory

Electron microscopy rarely contributory

t(X;18)

Characteristic histological appearances in benign areas