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Published on: December 19, 2019
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Primary cutaneous apocrine carcinoma: A challenging case report
Nayssem Khessairi1, Yasmine Fertani1, Saida Sakhri1
1Surgical Oncology Department, Salah Azaïz Institute, Tunis, Tunisia; University of Tunis El-Manar, Faculty of medicine of Tunis, Tunisia.
International Journal of Surgery Case Reports
|March 22, 2024
Summary
This case report details a rare primary cutaneous apocrine adenocarcinoma of the axilla in a male patient. Accurate diagnosis requires careful clinico-pathological correlation to differentiate from breast cancer metastases.
Area of Science:
- Dermatology
- Oncology
- Pathology
Background:
- Primary cutaneous apocrine carcinomas are rare adnexal tumors.
- Distinguishing them from breast cancer metastases is diagnostically challenging.
- Fewer than 200 cases have been reported in the literature.
Observation:
- A 58-year-old man presented with a large axillary mass.
- Initial biopsy suggested metastatic breast cancer, but imaging and tumor markers were negative.
- Histopathology and immunohistochemistry confirmed primary cutaneous apocrine adenocarcinoma.
Findings:
- The axillary tumor exhibited high CK7 expression and negative expression for TTF1, RH, PSA, and CK20.
- This immunoprofile aided in differentiating it from metastatic disease.
- The patient underwent surgical excision and axillary lymph node dissection.
Implications:
- This case highlights the importance of clinico-pathological correlation in diagnosing rare skin cancers.
- Careful histological analysis and clinical presentation are crucial for accurate diagnosis.
- Standard treatment involves wide local excision, potentially with lymph node dissection.

