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- W2937641383 abstract "<br>A unique case of eyelid metastasis from nasopharyngeal chondroid chordoma in a 63-year-old woman was reported. Chordomas are rare tumors of the bone deriving from remnants of the embryonic notochord. Histologically, the tumor showed lobulated structure and concludes two types of cells: liquid drop cell and small round/cubic cell. Immunohistochemically, AE1/AE3, epithelial membrane antigene (EMA), and S100 showed a uniform and strong positivity. It has a great capacity for recurrence and malignant transformation, despite their slow-growing nature. The most common sites of metastases are liver, lungs, and bones. The eyelid metastasis from chordoma is an extremely rare finding, which may suggest a poor prognosis for the patient. Its significant clinicopathological characteristic could prompt us to take it into consideration when assessing the patient's prognosis.<br>" @default.
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- W2937641383 date "2019-01-01" @default.
- W2937641383 modified "2023-10-18" @default.
- W2937641383 title "A unique case of eyelid metastasis from chondroid chordoma" @default.
- W2937641383 doi "https://doi.org/10.4103/ijpm.ijpm_387_18" @default.
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