Nuestro grupo organiza más de 3000 Series de conferencias Eventos cada año en EE. UU., Europa y América. Asia con el apoyo de 1.000 sociedades científicas más y publica más de 700 Acceso abierto Revistas que contienen más de 50.000 personalidades eminentes, científicos de renombre como miembros del consejo editorial.

Revistas de acceso abierto que ganan más lectores y citas
700 revistas y 15 000 000 de lectores Cada revista obtiene más de 25 000 lectores

Indexado en
  • Índice Copérnico
  • Google Académico
  • Abrir puerta J
  • Revista GenámicaBuscar
  • InvestigaciónBiblia
  • Biblioteca de revistas electrónicas
  • Búsqueda de referencia
  • Universidad Hamdard
  • EBSCO AZ
  • OCLC-WorldCat
  • Catálogo en línea SWB
  • Biblioteca Virtual de Biología (vifabio)
  • publones
  • Fundación de Ginebra para la educación y la investigación médicas
  • ICMJE
Comparte esta página

Abstracto

Pancreatic Squamous Cell Carcinoma: A Case Report and Review of the Literature

Fadwa Oudad, Nezha Tawfiq, Zineb Bouchbika, Nadia Benchakroun, Hassan Jouhadi, Souha Sahraoui, Abdellatif Benider

Background: Pancreatic squamous cell carcinoma is an exceptional disease. The pancreas is completely devoid of squamous cells, the development of squamous cell carcinoma at its level is controversial and of unknown origin. Squamous metaplasia of ductal cells has been observed in inflammatory episodes of pancreatic tissue. However, transformation to a squamous cell carcinoma remains exceptional. It is a very aggressive disease, most often locally advanced or metastatic at the time of diagnosis, and not very sensitive to the treatments offered.

Case Presentation: We describe here a case of a 64-year-old woman treated for a locally advanced pancreatic squamous cell carcinoma revealed by just diffuse abdominal pain. The diagnosis was confirmed by a peritoneal biopsy. She underwent palliative chemotherapy according to the protocol Capecitabine-Cisplatin, but the outcome was pejorative since she showed after 4 cures an enormous progression, preventing her from trying out another drug.

Conclusion: Due to the rarity of primary breast neuroendocrine tumors, no standard therapy exists.

We want to show through this case the pejorative prognosis of this rare tumor, and to motivate further prospective works in order to finally establish a better protocol to enhance our patients’ outcomes.