Thymoma (TMA)


Thymoma (TMA): Clinical Overview, Pathology, and Management
Thymoma (TMA) is a rare, thymic epithelial neoplasm arising from the thymus, often linked to autoimmune disorders like myasthenia gravis (MG). Below is a synthesis of its key aspects, supported by current evidence.
Clinical Features
- Demographics:
- Symptoms:
- Asymptomatic: ~30–50% of cases, detected incidentally via imaging26.
- Symptomatic:
- Local compression: Dysphagia, cough, chest pain, or superior vena cava syndrome26.
- Autoimmune associations:
- Myasthenia gravis (MG): Occurs in 30–45% of thymoma patients and 10–15% of MG patients27.
- Other syndromes: Pure red cell aplasia, Good syndrome, lupus, or rheumatoid arthritis23.
Pathology and Classification
Gross Features
- Encapsulation: Most are well-circumscribed with fibrous capsules14.
- Cut surface: Lobulated, gray-white to light brown, with possible cystic changes or hemorrhage18.
Microscopic Features
Thymomas exhibit organotypic thymic features, including lobular architecture, medullary differentiation, and dual epithelial-lymphoid cell populations14.
WHO 2021 Classification | Key Characteristics |
---|---|
Type A | Spindle/oval epithelial cells, rare thymocytes, bland cytology. |
Type AB | Mixed A and B1/B2 components. |
Type B | Polygonal epithelial cells, variable thymocyte density. Subtypes: B1 (medullary islands), B2 (mixed), B3 (epithelial-rich)48. |
Diagnosis
- Imaging:
- CT scan: Assesses tumor size, invasion, and metastasis (e.g., pleural deposits)26.
- Biopsy:
- Laboratory Tests:
- Autoantibodies: Acetylcholine receptor antibodies (for MG)27.
- Staging:
Management
- Surgical Resection:
- Chemotherapy:
- Adjuvant: For invasive or metastatic cases (e.g., cisplatin, doxorubicin)7.
- Autoimmune Management:
- MG: Immunosuppressants (e.g., prednisone) or thymectomy if refractory27.
Prognosis
- Stage-dependent: Early-stage (I–II) thymomas have 5-year survival rates >90%17.
- Autoimmune impact: MG improves post-thymectomy in ~30–50% of cases27.
Conclusion
Thymoma is a heterogeneous neoplasm with variable clinical behavior, often linked to autoimmune syndromes. Early diagnosis and surgical resection are critical for optimizing outcomes.
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References