Your browser doesn't support javascript.
loading
Rectal neuroendocrine neoplasia: a rare tumour.
de Benito Sanz, Marina; Santos Fernández, Javier; Núñez Rodríguez, Mª Henar.
Affiliation
  • de Benito Sanz M; Aparato digestivo, Hospital Rio Hortega.
  • Santos Fernández J; Aparato Digestivo, Hospital Río Hortega.
  • Núñez Rodríguez MH; Aparato digestivo, Hospital Río Hortega.
Rev Esp Enferm Dig ; 109(1): 79-80, 2017 01 15.
Article in En | MEDLINE | ID: mdl-27822951
ABSTRACT
Colorectal neuroendocrine tumours are rare A 78 year old man with a history of hypertension, heart disease, pacemakers, prostate adenocarcinoma.On examination for rectal bleeding, a colonoscopy was performed and at 5 cm of the anal margin a 28 mm ulcerated neoformation was found.An echo-endoscopy revealed infiltration of the muscular layer with an area of loss in the cleavage plane loss and fraying of the perirectal fat infiltration suggestive of infiltration (T3). They no lymph nodes or metastasis were identified by CAT. Radiotherapy treatment is ruled out due to having had it previously on the prostate and a proctectomy was opted for with mesorectal resection and Hartmann intervention. The pathology report revealed a large cell neuroendocrine carcinoma with numerous implants in perirectal adipose tissue and lymph metastasis in 2 lymph nodes (pT4aN1b), positive for synaptophysin, chromogranin and CD 56 with proliferation index Ki-67 50%.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Rectal Neoplasms / Neuroendocrine Tumors Type of study: Prognostic_studies Limits: Aged / Humans / Male Language: En Journal: Rev Esp Enferm Dig Journal subject: GASTROENTEROLOGIA Year: 2017 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Rectal Neoplasms / Neuroendocrine Tumors Type of study: Prognostic_studies Limits: Aged / Humans / Male Language: En Journal: Rev Esp Enferm Dig Journal subject: GASTROENTEROLOGIA Year: 2017 Document type: Article