A rare case of chordoma cutis.
Dayeon JungSeung Min KoJinwon SeoEun Joo ParkKwang Joong KimKwang Ho KimPublished in: Journal of cutaneous pathology (2023)
Chordoma is a rare locally aggressive bone malignancy that originates from the notochord. It typically involves the sacrococcygeal area, spheno-occipital region of the skull, and spine. Cutaneous involvement of chordoma, termed as chordoma cutis, is uncommon and usually occurs via direct invasion or local recurrence. Distant metastasis to the skin is very rare. We report a case of chordoma cutis on the scalp, which lacked characteristic physaliferous cells but tested positive for brachyury, thus supporting the diagnosis of chordoma cutis. The patient, who presented with a solitary translucent nodule on the scalp, was previously diagnosed with chordoma on the vertebral column and skull 8 months prior. Microscopic examination showed a cord-like arrangement of plasmacytoid cells within a myxoid stroma. Physaliferous cells were not observed, and cytokeratin AE1/AE3 staining was negative; however, brachyury and epithelial membrane antigen staining was positive, leading to the diagnosis of chordoma cutis. Therefore, clinicians must include chordoma cutis in the differential diagnosis of translucent nodular lesions on the skin of patients formerly diagnosed with chordoma.
Keyphrases
- induced apoptosis
- cell cycle arrest
- rare case
- dendritic cells
- end stage renal disease
- chronic kidney disease
- newly diagnosed
- oxidative stress
- lymph node
- bone mineral density
- endoplasmic reticulum stress
- cell death
- immune response
- mass spectrometry
- cell proliferation
- peritoneal dialysis
- case report
- wound healing
- body composition
- free survival
- simultaneous determination
- liquid chromatography