Báo cáo y học: "Fast-growing pancreatic neuroendocrine carcinoma in a patient with multiple endocrine neoplasia type 1: a case report"

Tuyển tập báo cáo các nghiên cứu khoa học quốc tế ngành y học dành cho các bạn tham khảo đề tài: Fast-growing pancreatic neuroendocrine carcinoma in a patient with multiple endocrine neoplasia type 1: a case report | Journal of Medical Case Reports BioMed Central Open Access Fast-growing pancreatic neuroendocrine carcinoma in a patient with multiple endocrine neoplasia type 1 a case report Jens Waldmann 1 Nils Habbe1 Volker Fendrich1 Emily P Slater1 Peter H Kann2 Matthias Rothmund1 and Peter Langer1 Address Department of General Surgery University Hospital Giessen and Marburg Marburg Baldingerstrasse 35037 Marburg Germany and department of Internal Medicine Division of Endocrinology and Diabetology University Hospital Giessen and Marburg Baldingerstrasse 35037 Marburg Germany Email Jens Waldmann - jwaldman@ Nils Habbe - habbe@ Volker Fendrich - fendrich@ Emily P Slater - slater@ Peter H Kann - kannp@ Matthias Rothmund - rothmund@ Peter Langer - langerp@ Corresponding author Published 18 November 2008 Received 3 December 2007 _ __n inno Ajmrj Accepted 18 November 2008 Journal of Medical Case Reports 2008 2 354 doi l752-l947-2-354 This article is available from http content 2 l 354 2008 Waldmann et al licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License http licenses by which permits unrestricted use distribution and reproduction in any medium provided the original work is properly cited. Abstract Introduction Predictive genetic screening and regular screening programs in patients with multiple endocrine neoplasia type l are intended to detect and treat malignant tumors at the earliest stage possible. Malignant neuroendocrine pancreatic tumors are the most frequent cause of death in these patients. However the extent and intervals of screening in patients with multiple endocrine neoplasia type l are controversial as neuroendocrine tumors are usually slow growing. Here we report the case of a patient who developed a .

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