Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 4 de 4
Filtrar
Mais filtros

Base de dados
Tipo de documento
Intervalo de ano de publicação
4.
Ophthalmic Plast Reconstr Surg ; 34(3): e86-e88, 2018.
Artigo em Inglês | MEDLINE | ID: mdl-29505467

RESUMO

Merkel cell carcinoma is a rare neuroendocrine tumor of subspecialized dermal mechanoreceptors, associated with immunosuppression. The usual ophthalmic presentation is an eyelid lesion. The authors present a case of biopsy-proven orbital metastatic Merkel cell carcinoma in the absence of any eyelid lesion, in an immunosuppressed patient with a history of multiple cancers. There are to the authors' knowledge only 2 other case reports of presumed metastatic Merkel cell carcinoma to the orbit, though neither were biopsied. Despite its rarity, metastatic Merkel cell carcinoma should be included in the differential of a metastatic orbital lesion, in the patient with a known or suspected cutaneous primary. The patient has had an excellent response to combined radiotherapy and programmed death-1 inhibitor pembrolizumab, and this case highlights the potential benefit of an exciting new biologic therapy.


Assuntos
Carcinoma de Célula de Merkel/secundário , Neoplasias Orbitárias/secundário , Carcinoma de Célula de Merkel/patologia , Humanos , Masculino , Pessoa de Meia-Idade , Neoplasias Orbitárias/patologia
SELEÇÃO DE REFERÊNCIAS
DETALHE DA PESQUISA