Type C thymoma
Type C Thymoma is a rare type of thymoma, a tumor originating from the thymus. It is also known as thymic carcinoma. This type of thymoma is characterized by its aggressive behavior and poor prognosis compared to other types of thymomas.
Classification[edit | edit source]
Type C Thymoma is classified under the World Health Organization's (WHO) histological classification of thymomas. The WHO classification divides thymomas into five categories: Type A, AB, B1, B2, and B3. Type C is a separate category, representing thymic carcinomas.
Symptoms[edit | edit source]
Patients with Type C Thymoma may present with symptoms such as cough, chest pain, and shortness of breath. Some patients may also have myasthenia gravis, a neuromuscular disorder that causes weakness in the skeletal muscles.
Diagnosis[edit | edit source]
The diagnosis of Type C Thymoma is made based on the histological examination of the tumor. Immunohistochemistry is often used to differentiate Type C Thymoma from other types of thymomas.
Treatment[edit | edit source]
The primary treatment for Type C Thymoma is surgical resection of the tumor. Chemotherapy and radiation therapy may also be used in some cases.
Prognosis[edit | edit source]
The prognosis for patients with Type C Thymoma is generally poor due to the aggressive nature of the tumor. The 5-year survival rate is significantly lower than for other types of thymomas.
See also[edit | edit source]
Type C thymoma Resources | |
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Contributors: Prab R. Tumpati, MD