Results 21 to 30 of about 5,234,907 (203)

Merkel Cell Carcinoma [PDF]

open access: yesJournal of the National Comprehensive Cancer Network, 2009
Merkel cell carcinoma (MCC), also known as primary neuroendocrine skin carcinoma or Merkel cell tumor, is a cutaneous malignancy of neuroendocrine origin, first described by Toker in 1972. Although MCC is rare, it has been shown to have a higher mortality rate than malignant melanoma with a 5-year disease-specific survival rate of 64% [1].
Stanley J, Miller   +25 more
  +7 more sources

Merkel cell carcinoma

open access: yesDermatologic Therapy, 2008
Merkel cell carcinoma is a rare cutaneous malignancy that occurs mainly in the ultraviolet-exposed areas of the head and neck region and has a mortality rate higher than that of melanoma (33%) with a tendency to recur. The clinical features, diagnosis, work up, and current recommendations for treatment of Merkel cell carcinoma are discussed.
Viola, G.   +4 more
  +7 more sources

Promoter activity of Merkel cell Polyomavirus variants in human dermal fibroblasts and a Merkel cell carcinoma cell line. [PDF]

open access: yes, 2020
Background - Merkel cell polyomavirus (MCPyV) is a human polyomavirus that establishes a life-long harmless infection in most individuals, with dermal fibroblasts believed to be the natural host cell. However, this virus is the major cause of Merkel cell
Moens, Ugo   +5 more
core   +1 more source

Merkel cell carcinoma

open access: yesTidsskrift for Den norske legeforening, 2022
Merkel cell carcinoma is an uncommon but aggressive tumour with a high metastatic potential. A rapidly growing, non-tender cutaneous tumour on sun-exposed areas of the body in older patients should raise suspicion of the condition. It may be necessary to combine the patient history with clinical, radiological and pathological findings in order to make ...
Morten Kristoffer, Nyrud   +6 more
openaire   +2 more sources

CCL17/TARC and CCR4 expression in Merkel cell carcinoma [PDF]

open access: yes, 2018
Merkel cell carcinoma (MCC) is a rare, highly aggressive neuroendocrine skin cancer. In more than 80% of the cases, Merkel cell polyomavirus (MCPyV) is a causal factor.
Grimstad, Øystein   +5 more
core   +1 more source

Primary Merkel cell carcinoma of the salivary gland: a clinicopathologic study of four cases with a review of literature [PDF]

open access: yesJournal of Pathology and Translational Medicine
Background Primary Merkel cell carcinoma of the salivary gland is currently not listed in the World Health Organization classification. However, cases of Merkel cell type neuroendocrine carcinomas of the salivary gland with perinuclear cytokeratin 20 ...
Gyuheon Choi   +6 more
doaj   +1 more source

Extensive central nervous system involvement in Merkel cell carcinoma: a case report and review of the literature

open access: yesJournal of Medical Case Reports, 2011
Introduction Merkel cell carcinoma is a rare malignant cutaneous neoplasm that is locally invasive and frequently metastasizes to lymph nodes, liver, lungs, bone and brain.
Söderström Kristina   +2 more
doaj   +1 more source

Kidney metastasis in a case of Merkel cell carcinoma

open access: yesUrology Case Reports, 2021
Merkel cell carcinoma is a rare neuroendocrine skin tumor with a poor prognosis. Metastasis is frequent and is seen in the first few years after diagnosis.
Abdessamade Motaouakil   +5 more
doaj   +1 more source

Merkel cell carcinoma metastasis and dermatofibrosarcoma protuberans presenting as a collision tumour: a case report and review of the literature

open access: yesJournal of Medical Case Reports, 2009
Introduction Merkel cell carcinoma and dermatofibrosarcoma protuberans are two very rare neoplasms. The simultaneous occurrence of two different tumour entities at the same anatomical site, collision tumours, is a rare phenomenon.
Tilkorn Daniel-Johannes   +6 more
doaj   +1 more source

Merkel Cell Carcinoma

open access: yesArchives of Pathology and Laboratory Medicine, 2010
Abstract Merkel cell carcinoma is a rare, highly aggressive neuroendocrine cutaneous neoplasm with a variable clinical presentation. Histologically, it is a predominantly dermal-based lesion composed of monotonous small round cells with scanty cytoplasm, often difficult to differentiate from small round cell tumors, metastatic small ...
Hannah H, Wong, Jun, Wang
openaire   +4 more sources

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