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Merkel cell carcinoma (MCC) is a rare and aggressive skin cancer occurring in about three people per million members of the population. [1] It is also known as cutaneous APUDoma, primary neuroendocrine carcinoma of the skin, primary small cell carcinoma of the skin, and trabecular carcinoma of the skin. [2]
Merkel cell carcinoma pictures. The appearance of Merkel cell carcinoma can vary. However, a bump may look like this: BSIP - Getty Images. How is Merkel cell carcinoma diagnosed and treated?
Merkel cell carcinoma accounts for fewer than 1% of all skin cancers — but when it metastasizes it often turns deadly. Merkel cell carcinoma accounts for fewer than 1% of all skin cancers ...
Merkel cell carcinoma is a highly aggressive type of skin cancer that was first described by Cyril Toker in 1972 as "trabecular tumor of the skin". [20] Based on its origin, the cancer cell type is called a neuroectodermal tumor.
Cancer Research UK has recently warned that skin cancer cases are set to rise by half by 2040
Merkel cell carcinoma (cutaneous apudoma, primary neuroendocrine carcinoma of the skin, primary small cell carcinoma of the skin, trabecular carcinoma of the skin) Microcystic adnexal carcinoma (sclerosing sweat duct carcinoma) Micronodular basal cell carcinoma; Milia en plaque; Milium Milium; Mixed tumor (chondroid syringoma) Mucinous carcinoma
Rare and deadly type of skin cancer doesn't look like other types.
Merkel cells, also known as Merkel–Ranvier cells or tactile epithelial cells, are oval-shaped mechanoreceptors essential for light touch sensation and found in the skin of vertebrates. They are abundant in highly sensitive skin like that of the fingertips in humans , and make synaptic contacts with somatosensory afferent nerve fibers .