首页 文献索引 SCI期刊 AI助手
期刊目录筛选

期刊名:Surgical clinics of north america

缩写:SURG CLIN N AM

ISSN:0039-6109

e-ISSN:1558-3171

IF/分区:2.8/Q1

文章目录 更多期刊信息

共收录本刊相关文章索引1596
Clinical Trial Case Reports Meta-Analysis RCT Review Systematic Review
Classical Article Case Reports Clinical Study Clinical Trial Clinical Trial Protocol Comment Comparative Study Editorial Guideline Letter Meta-Analysis Multicenter Study Observational Study Randomized Controlled Trial Review Systematic Review
Kailey M Oppat,Frances J Bennett,Shishir K Maithel Kailey M Oppat
With improvements in surgical technique and advances in pancreatic endocrine and exocrine replacement therapy, the indications for, and threshold to perform, total or completion pancreatectomy in the modern surgical era are ever evolving. T...
Justin Drake,Daniel A Anaya,Jason B Fleming et al. Justin Drake et al.
Pancreaticoduodenectomy, first described in 1935, has subsequently been refined over decades into the operation performed today for tumors of the pancreatic head and periampullary region. For years following Whipple's first publication, tum...
Brittany C Fields,Ching-Wei D Tzeng Brittany C Fields
Locally advanced pancreatic cancer (LAPC) represents a unique clinical scenario in which the tumor is considered localized but unresectable due to anatomic factors. Despite a consensus against upfront surgery, no standard approach to induct...
Samuel Keltner,Bailey Nelson,Jordan Kharofa Samuel Keltner
Pancreatic adenocarcinoma remains a deadly disease with 5 year overall survival of 10% among all stages. Standard of care for resectable disease remains surgical resection and adjuvant systemic therapy, but paradigms for borderline resectab...
Adriana Ramirez,Fiemu Nwariaku,Tricia Moo-Young et al. Adriana Ramirez et al.
While there has been great progress in the past few decades in the management of endocrine surgery disorders, with adoption of new technologies and approaches, standardization of practice patterns, and guideline recommendations, unequal imp...
C Corbin Frye,Taylor C Brown,John A Olson Jr C Corbin Frye
Multiple endocrine neoplasia (MEN) syndromes are rare autosomal dominant diseases that are associated with a mixture of both endocrine and non-endocrine tumors. Traditionally, there are 2 types of MEN that have unique clinical associations:...
Shadin Ghabra,Bhavishya Ramamoorthy,Stephen G Andrews et al. Shadin Ghabra et al.
Pancreatic neuroendocrine tumors (PNETs) arise from neuroendocrine cells and are a rare class of heterogenous tumors with increasing incidence. The diagnosis, staging, treatment, and prognosis of PNETs depend heavily on identifying the hist...
Joseph Tobias,Xavier M Keutgen Joseph Tobias
Pancreatic neuroendocrine tumors originate from hormone-producing islet cells and have a propensity to metastasize to the liver once they reach 2 cm in size. Their diagnosis relies upon a combination of computed tomography, MRI, DOTATATE PE...