کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
9244272 | 1209908 | 2005 | 17 صفحه PDF | دانلود رایگان |
عنوان انگلیسی مقاله ISI
Enteroendocrine Tumors Other Than Carcinoid: A Review of Clinically Significant Advances
دانلود مقاله + سفارش ترجمه
دانلود مقاله ISI انگلیسی
رایگان برای ایرانیان
کلمات کلیدی
CGASSTSRSAPUDChromogranin-ASSTRGEPMEN-1Pancreatic endocrine tumor - تومور غدد درون ریز پانکراسNeuroendocrine tumor - تومور نورو اندوکرینamine precursor uptake and decarboxylation - جذب پیشگیر آمین و دکربوکسیلیک کردنNET - خالصZollinger-Ellison syndrome - سندرم Zollinger-EllisonSomatostatin - سوماتواستاتینSomatostatin receptor scintigraphy - سینتیگرافی گیرنده سموتوستاتینZES - ششPET - پتGastroenteropancreatic - گاستروانترپانکراسیSomatostatin receptor - گیرنده سوماتوستاتین
موضوعات مرتبط
علوم پزشکی و سلامت
پزشکی و دندانپزشکی
بیماریهای گوارشی
پیش نمایش صفحه اول مقاله

چکیده انگلیسی
Only relatively recently has there been an increased clinical recognition and characterization of the heterogenous group of rare gastroenteropancreatic neuroendocrine neoplasms. Most have endocrine function and exhibit varying degrees of malignancy. This review summarizes the derivation of these tumors and the advances in their diagnosis and treatment over the past decade and a half. They are varied in their biological behavior and clinical courses and, depending on their cell type, can produce different hormones causing distinct clinical endocrine syndromes (insulinoma [hypoglycemia], gastrinoma [Zollinger-Ellison syndrome (ZES)], vasoactive intestinal peptideoma [VIPoma], watery diarrhea, hypokalemia-achlorhydria [WDHA], glucagonoma [glucagonoma syndrome], and so forth). In addition to surgery for cure or palliation (by excision and a variety of other cytoreductive techniques), they each are treated with antihormonal agents or drugs targeted to each tumor's specific product or its effects. The majority have benefited from the gut hormone-inhibiting action of somatostatin analogs. Because of their usual slow rate of growth it is recommended that, even when they are advanced and incurable, unlike in patients with common and more malignant cancers, patients with neuroendocrine tumors often can be palliated and appear to survive longer when managed with an active approach using sequential multimodality treatment. Advances in these various therapies are reviewed and the beneficial emergence of global self-help patient support groups is noted.
ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Gastroenterology - Volume 128, Issue 6, May 2005, Pages 1668-1684
Journal: Gastroenterology - Volume 128, Issue 6, May 2005, Pages 1668-1684
نویسندگان
Richard R.P. Warner,