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Appendiceal neuroendocrine neoplasia: analysis of 50 patients.
Cir Cir
December 2022
Department of General Surgery, Ankara City Hospital, Ankara. Turkey.
Objective: The objective of this study was to investigate the clinical, surgical, and pathological findings of appendiceal neuroendocrine neoplasms (ANNs).
Materials And Methods: The demographic, clinical, surgical, and pathological characteristics of 50 patients with ANN were analyzed. The patients were also classified as Group 1 (< 40 years, n = 37) and Group 2 (≥ 40 years, n = 13), and compared each other in terms of all parameters.
Surgical options for the treatment of neuroendocrine neoplasms of the ampulla of Vater: a reference centre experience.
Cir Esp (Engl Ed)
July 2023
Servicio de Cirugia General y del Aparato Digestivo, Unidad de Cirugía Hepatobiliopancreática y Trasplante Hepático, Hospital Universitari de Bellvitge, Spain; Departamento de Ciencias Clínicas, Facultat de Medicina i Ciències de la Salut, Universitat de Barcelona, Spain; Research Group of Hepato-biliary and Pancreatic Diseases, Institut d'Investigació Biomèdica de Bellvitge - IDIBELL, Spain.
Introduction: The main objective of this study was to analyse the results of the surgical treatment of ampullary neuroendocrine tumours (NET) based on transduodenal ampullectomy and pancreatoduodenectomy, in a reference centre in hepatobiliopancreatic pathology.
Method: Retrospective, observational study, including all patients operated on for pancreatic and/or duodenal NET in a reference unit of hepatobiliopancreatic pathology and prospectively registered between January 1st, 1993 and September 30th, 2021. For those parameters not present, retrospective research was performed.
Sclerosing pneumocytoma with carcinoid tumorlets and neuroendocrine cell hyperplasia.
Rev Esp Patol
September 2022
Patología, Hospital General Universitario de Alicante, Spain. Electronic address:
Sclerosing pneumocytoma is an uncommon pulmonary tumor which generally behaves benignly and occurs predominately in women. Rarely, it is associated with neuroendocrine proliferations such as hyperplasia, tumorlets and carcinoid tumors, which may be observed in relation to the tumor or in the distant lung parenchyma; the mechanism underlying this neuroendocrine differentiation is not clear. We present a case of a 33 year-old male with sclerosing pnemocytoma with coexistent neuroendocrine hyperplasia and combined carcinoid tumorlets.
View Article and Find Full Text PDFNeoplasia neuroendocrina metastásica de origen desconocido: de la incertidumbre en el diagnóstico por imagen a la precisión de la cirugía radioguiada laparoscópica.
Rev Esp Med Nucl Imagen Mol (Engl Ed)
July 2022
Unidad de Cirugía HBP, Servicio de Cirugía General y del Aparato Digestivo, Hospital Universitario Virgen de la Victoria, Málaga, Spain.
[Small bowel obstruction caused by lymph nodes of a neuroendocrine tumor. A clinical case report].
Rev Med Chil
March 2021
Servicio de Anatomía Patológica, Hospital Militar de Santiago, Santiago, Chile.
Small intestine neuroendocrine tumors (NET-SI) are relatively rare neoplasms. If encountered, the most common location is the ileum. Symptoms are usually non-specific, delaying the tumors diagnosis.
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