Clinicopathologic study of epithelioid sarcoma
Dan Li
Abstract
Dan Li
Abstract
Objective:To study the clinicopathologic features、diagnosis and differential diagnosis of epithelioid sarcoma.Methods:Two cases of epithelioid sarcoma were collected according to the classification of soft tissue and bone tumors(WHO,2002) and were studied by hematoxylin-eosin and immunohistochemical staining.Results:One case was proximal type epithelioid sarcoma,and the other distal type epithelioid sarcoma.The case of distal type epithelioid sarcoma was female,twenty eight years old,and the site was the left leg;histological structure was the typical pseudo-granuloma formation,the tumor cells resembled epithelioid cells,with necrosis in the center.The case of proximal type epithelioid sarcoma was female,thirty six years old,and the site was the cervix;nodal formation can be observed,the tumor cells resembled spindle cells,abd the extent of necrosis was bigger.For the immunohistochemical staining,expressions of Vimentin、EMA and CK antigen were observed in the 2 cases,while expressions of Desmin、NSE and S-100 antigen were negative.Moreover,expressions of low CK and CD34 antigen were also observed in the case of distal type epithelioid sarcoma.On the other hand,expressions of Actin、SMA and HMB-45 antigen were not observed in the case of proximal type epithelioid sarcoma.Conclusions:Epithelioid sarcoma is a rare maliglant tumor of soft tissue,It's the key for diagnosis and differential diagnosis to combine clinic、histological structure、immunophenotype and prognosis together.
A significance statement is not available in the OpenAlex record.
A contribution statement is not available in the OpenAlex record.
Method details are not available in the OpenAlex metadata.
Findings are not separately available in the OpenAlex metadata.
Limitations are not available in the OpenAlex metadata.
Application details are not available in the OpenAlex metadata.
Objective:To study the clinicopathologic features、diagnosis and differential diagnosis of epithelioid sarcoma.Methods:Two cases of epithelioid sarcoma were collected according to the classification of soft tissue and bone tumors(WHO,2002) and were studied by hematoxylin-eosin and immunohistochemical staining.Results:One case was proximal type epithelioid sarcoma,and the other distal type epithelioid sarcoma.The case of distal type epithelioid sarcoma was female,twenty eight years old,and the site was the left leg;histological structure was the typical pseudo-granuloma formation,the tumor cells resembled epithelioid cells,with necrosis in the center.The case of proximal type epithelioid sarcoma was female,thirty six years old,and the site was the cervix;nodal formation can be observed,the tumor cells resembled spindle cells,abd the extent of necrosis was bigger.For the immunohistochemical staining,expressions of Vimentin、EMA and CK antigen were observed in the 2 cases,while expressions of Desmin、NSE and S-100 antigen were negative.Moreover,expressions of low CK and CD34 antigen were also observed in the case of distal type epithelioid sarcoma.On the other hand,expressions of Actin、SMA and HMB-45 antigen were not observed in the case of proximal type epithelioid sarcoma.Conclusions:Epithelioid sarcoma is a rare maliglant tumor of soft tissue,It's the key for diagnosis and differential diagnosis to combine clinic、histological structure、immunophenotype and prognosis together.
Key concepts: Epithelioid sarcoma, Pathology, Sarcoma, Differential diagnosis, Epithelioid cell, Vimentin, Medicine, Immunohistochemistry