Abstract
Thymoliposarcoma is an exceedingly rare thymic neoplasm with only five reports in English literature to date. We report another patient, a 36-year-old male, who developed local recurrences 4-years after initial resection. The clinicopathologic features of the present and previously reports were compared with particular emphasis on their morphologic spectrum and differential diagnosis.
| Original language | English |
|---|---|
| Pages (from-to) | 2082-2085 |
| Number of pages | 4 |
| Journal | Annals of Thoracic Surgery |
| Volume | 76 |
| Issue number | 6 |
| DOIs | |
| State | Published - 12 2003 |
| Externally published | Yes |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 3 Good Health and Well-being
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