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비전형적인 임상양상을 보이는 Merkel 세포암 1예A case of merkel cell carcinoma with unusual clinical manifestation

Authors
Cho, W.I.Seo, S.J.Hong, C.K.Song, K.Y.
Issue Date
Jan-2006
Publisher
대한피부과학회
Keywords
Merkel cell carcinoma; Pain; Unusual clinical manifestation
Citation
Korean Journal of Dermatology, v.44, no.1, pp 106 - 108
Pages
3
Journal Title
Korean Journal of Dermatology
Volume
44
Number
1
Start Page
106
End Page
108
URI
https://scholarworks.bwise.kr/cau/handle/2019.sw.cau/25540
ISSN
0494-4739
Abstract
Merkel cell carcinoma is a rare, aggressive skin cancer that occurs most frequently in the elderly on sun-exposed areas. However, any possible cutaneous or mucosal sites may also be involved. It usually presents as a rapidly-growing, painless, single red or purple colored cutaneous papule, nodule or indurated plaque that may elude diagnosis until histopathologic examination. We report a case of an 83-year old female patient who presented with a 3 × 3.5 cm sized, skin-colored, painful nodule on the left mandibular angle area. A new red nodule had combined on the original lesion after 6 months, and showed unusual clinical manifestation. Microscopically, the tumor cells were uniform with round to oval-shaped nuclei and scanty cytoplasm, and they showed a trabecular arrangement. In immunohistochemical studies, the patient was reactive to cytokeratin-20, and focally reactive to NSE and synaptophysin.
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