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Published on: October 2, 2014
Metachronous multiple thymoma with different clinical behavior and pathological findings
Tomonari Oki1, Toru Nakamura1, Yoshifumi Arai2
11Department of General Thoracic Surgery, Seirei Hamamatsu General Hospital, Sumiyoshi 2-12-12, Naka-ku, Hamamatsu, Shizuoka 430-8558 Japan.
This study presents a rare case of multicentric thymoma in a 70-year-old woman. Two distinct thymomas, a stage 1 type B2 and a stage 3 type B3, were found, suggesting independent origins.
Area of Science:
- Thoracic oncology
- Pathology
- Surgical oncology
Background:
- Thymoma is a rare tumor originating from the thymus.
- Multicentric thymoma, with multiple distinct primary tumors, is exceptionally rare.
Observation:
- A 70-year-old woman presented with sequential development of two distinct masses in the left hilum.
- Initial nodule identified on chest radiograph 3 years prior, followed by a second mass.
- Surgical resection revealed an encapsulated rostral nodule and a caudal mass invading the left lung.
Findings:
- Histological examination identified the rostral nodule as a stage 1 type B2 thymoma.
- The caudal mass was diagnosed as a stage 3 type B3 thymoma.
- Significant differences in tumor encapsulation, invasiveness, and histological subtype were noted.
Implications:
- The distinct characteristics suggest a multicentric origin rather than intrapulmonary metastasis.
- This case highlights the importance of thorough pathological evaluation for thymic neoplasms.
- Understanding multicentric thymoma origins can inform future diagnostic and treatment strategies.
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