An 80-year-old Japanese man presented with a 10-year history of a slowly growing solitary tumor on his right parasternal region. A dermatological examination revealed a reddish erosive tumor, 20×19×5 mm in size, with oozing. No regional lymph node metastasis or other distant metastasis was detected. Under the clinical impression of sweat gland malignancy or amelanotic melanoma, the tumor was resected with a wide margin, and grafting was performed. Histopathological examination showed an asymmetric and elevated tumor with the main lesion located in the dermis. The tumor cells were arranged in a solid-nesting, trabecular, or ribbon-like appearance, which had comparatively regular oval nuclei and eosinophilic cytoplasm. Decapitation secretion was seen in part. Immunohistochemically, the tumor cells were positive for CAM5.2, EMA, gross cystic disease fluid protein-15, cytokeratin (CK)7, synaptophysin, chromogranin A, CD56, estrogen receptor, and progesterone receptor, and negative for CK20 and HER2. Further examination ruled out the existence of breast carcinoma. The patient was finally diagnosed with primary apocrine carcinoma with neuroendocrine differentiation. Sentinel node biopsy was not performed in accordance with the patient's wishes, and he took an anti-estrogen agent, tamoxifen, at 20 mg/day, after the diagnosis was made. No recurrence or metastasis of the tumor has been noted for 1 year and 8 months.[
Skin Cancer (Japan) 2014 ; 29 : 165-170]
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