Results 171 to 180 of about 29,157 (205)
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Merkel Cell Carcinoma

The Laryngoscope, 2004
AbstractPurpose: To determine the natural history and treatment outcomes for patients with Merkel cell carcinoma.Methods: Review of the literature.Results: The probability of regional node involvement at presentation exceeds 50%; few patients present with distant metastases.
William M, Mendenhall   +2 more
openaire   +4 more sources

Merkel Cell Carcinoma

Seminars in Oncology, 2007
Merkel cell carcinoma (MCC) is a rare, aggressive cutaneous cancer that predominately affects elderly Caucasians with fair skin and has a propensity for local recurrence and regional lymph node metastases. A variety of terms have been used to describe this tumor, including trabecular cell carcinoma, neuroendocrine or primary small cell carcinoma of the
Michael Howard, Swann, Jaeyoung, Yoon
openaire   +2 more sources

Merkel Cell Carcinomas

Hematology/Oncology Clinics of North America, 2007
Merkel cell carcinoma (MCC) is a rare and extremely aggressive skin cancer that arises from primary neural cells. It presents most commonly in the elderly and immunocompromised patients. Pathologically, MCC should be distinguished from extrapulmonary small cell lung cancer or metastatic small cell lung cancer or a small cell variant of melanoma.
Vy, Dinh   +3 more
openaire   +2 more sources

Merkel cell polyomavirus and Merkel cell carcinoma [PDF]

open access: yesPhilosophical Transactions of the Royal Society B: Biological Sciences, 2017
Merkel cell polyomavirus (MCPyV) causes the highly aggressive and relatively rare skin cancer known as Merkel cell carcinoma (MCC). MCPyV also causes a lifelong yet relatively innocuous infection and is one of 14 distinct human polyomaviruses species.
James A Decaprio
exaly   +3 more sources

MERKEL CELL CARCINOMA

Australian and New Zealand Journal of Surgery, 1998
Merkel cell carcinomas (MCCs) are rare cutaneous neuroendocrine neoplasms that are clinically aggressive due to a relatively high local, regional, and distant metastatic recurrence potential. They are found most commonly in Caucasian (94 %), elderly patients, with an average age at presentation being approximately 72 years.
D S, Cheung, I E, McInnes
openaire   +2 more sources

Merkel cell carcinoma

International Journal of Oral and Maxillofacial Surgery, 1992
A case of Merkel cell carcinoma of the cheek is described, highlighting the clinical behaviour, diagnosis and management of this uncommon tumour.
K, Altman, P J, Mahaffey
openaire   +2 more sources

Merkel cell carcinoma

Journal of the American Academy of Dermatology, 1993
Merkel cell carcinoma is a malignant neuroendocrine tumor with features of epithelial differentiation. Biologically aggressive, it may be difficult to diagnose and, particularly in its late stages, even more difficult to treat effectively. This article addresses what is known and what is still controversial about the histogenesis, diagnosis, and ...
D, Ratner   +3 more
openaire   +2 more sources

Merkel Cell Carcinoma

Dermatologic Surgery, 1996
Merkel cell carcinoma is an aggressive tumor with nonspecific clinical features. The prognosis in general is worse than malignant melanoma. Local recurrence rates are high with one-third of patients having recurrence within one year of excision. The tumor invades blood vessels and lymphatics.
W J, O'Connor, D G, Brodland
openaire   +2 more sources

Merkel cell carcinoma

Journal of Computed Tomography, 1987
Merkel cell carcinoma is a rare malignant neoplasm of the skin which is locally invasive and frequently metastasizes to lymph nodes, liver, lungs, bone, and brain. Computed tomographic and pathologic findings in an elderly woman with Merkel cell carcinoma of the buttock and regional nodal metastasis are reported.
S, Marks, D R, Radin, P, Chandrasoma
openaire   +2 more sources

Merkel Cell Carcinoma

Hematology/Oncology Clinics of North America, 2012
Merkel cell carcinoma (MCC) is a rare but aggressive carcinoma of the skin, arising most commonly in sun-exposed sites of elderly patients. The diagnosis is based on characteristic histopathologic features. In 2008, the discovery of the Merkel cell polyomavirus led to intensified research into the viral pathogenesisis of MCC.
Sandra Y, Han   +4 more
openaire   +2 more sources

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