Publication:
Merkel Cell Carcinoma

dc.contributor.authorSönmez Ergün, Selma
dc.contributor.authorKirazoğlu, Ahmet
dc.contributor.authorAkdemir, Osman Cemil
dc.contributor.authorSu Küçük, Özlem
dc.contributor.authorAltınok, Pelin
dc.contributor.authorYıldız, Pelin
dc.contributor.institutionauthorERGÜN, SELMA
dc.contributor.institutionauthorAKDEMİR, OSMAN CEMİL
dc.contributor.institutionauthorKİRAZOĞLU, AHMET
dc.contributor.institutionauthorYILDIZ, PELİN
dc.contributor.institutionauthorSU KÜÇÜK, ÖZLEM
dc.contributor.institutionauthorALTINOK SÜT, PELİN
dc.date.accessioned2023-03-01T21:30:43Z
dc.date.available2023-03-01T21:30:43Z
dc.date.issued2023-01-01
dc.description.abstractMerkel cell carcinoma (MCC) is a rare tumor that arises from mechanoreceptor Merkel cells. Ultraviolet exposure, immunosuppression and Merkel cell polyoma virus play a significant role in tumor pathogenesis. Although it typically presents as an initially indolent growing, painless solitary lesion, the course of MCC may be aggressive due to the nodal invasion, distant metastasis and high recurrence rates. We presented a case of MCC with a background history of rheumatoid arthritis treated with immunosuppressive therapy for many years who had necrotizing granulomatous lymphadenitis.
dc.identifier.citationSönmez Ergün S, Kirazoğlu A, Akdemir OC, Küçük ÖS, Altınok P, Yıldız P. Merkel Cell Carcinoma. Bezmialem Science 2023;11(1):128-31
dc.identifier.doi10.14235/bas.galenos.2022.08760
dc.identifier.endpage131
dc.identifier.issn2148-2373
dc.identifier.issue1
dc.identifier.startpage128
dc.identifier.urihttps://hdl.handle.net/20.500.12645/37708
dc.identifier.volume11
dc.relation.ispartofBEZMIALEM SCIENCE
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectMerkel cell carcinoma
dc.subjectimmunosuppression
dc.subjecttherapy
dc.titleMerkel Cell Carcinoma
dc.typearticle
dspace.entity.typePublication
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