American Cancer Society
January 1, 2001
Nghiem P, McKee PH, Haynes HA, In Sober AJ (eds), Haluska FG (eds)Download PDF
Merkel cell carcinoma (primary cutaneous neuroendocrine carcinoma, trabecular carcinoma) is a rare but often lethal tumor of uncertain histogenesis. Five cases were originally described by Toker in 1972 as “trabecular carcinoma of the skin.” This name was derived from the most characteristic (but least common) of three distinct histologic patterns for this tumor. Later electron microscopic analysis revealed cytoplasmic neurosecretory granules in the cells of this carcinoma and linked it to its most likely precursor, the Merkel cell. Pathologists suggest that this tumor should be called neuroendocrine carcinoma of the skin because it is highly analogous to such tumors in the lung (small cell carcinoma) and other sites, likely sharing a similar precursor cell.
The authoritative source on Merkel cell carcinoma.
September 22, 2020
- What is a Merkel cell?
- What is Merkel cell carcinoma?
- Symptoms & appearance of Merkel cell carcinoma
- Causes of Merkel cell carcinoma
- Surgical excision
- Mohs micrographic surgery
- Radiation therapy
- Complementary & alternative therapies
- Clinical trials
- Adjuvant Avelumab in Merkel Cell Carcinoma Trial