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Int J Surg Pathol ; 28(3): 325-329, 2020 May.
Artigo em Inglês | MEDLINE | ID: mdl-31601140

RESUMO

Merkel cell carcinoma (MCC) is a rare entity that most commonly arises from the skin. Angiosarcoma (AS) is a rare malignancy with a predilection for elderly males, has endothelial differentiation and a notoriously poor prognosis despite aggressive therapy. Herein, we report an angiosarcoma colliding with a MCC, in a patient with a past medical history of squamous cell carcinoma, status-post radiation therapy. More specifically, our case represents a collision tumor, a rare entity composed of two histologically distinct neoplasms which coincide together at the same location. This case represents the first documented report of such a presentation. With that being said, its clinical course, prognosis, pathogenesis, and molecular profile, currently remains unclear. Importantly, neoplasms are increasingly being found to be associated with radiation therapy, of which our patient had received. Ultimately, however, with the lack of c-MYC immunohistochemical staining, and a short duration between radiation exposure and presentation, the AS in our case was likely coincidental.


Assuntos
Carcinoma de Célula de Merkel/patologia , Hemangiossarcoma/patologia , Neoplasias Primárias Múltiplas/patologia , Neoplasias de Tecidos Moles/patologia , Idoso de 80 Anos ou mais , Humanos , Masculino , Neoplasias Induzidas por Radiação/patologia , Neoplasias Cutâneas/radioterapia , Neoplasias Cutâneas/cirurgia , Carcinoma de Células Escamosas de Cabeça e Pescoço/radioterapia , Carcinoma de Células Escamosas de Cabeça e Pescoço/cirurgia
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