The impact of failure to achieve symptom control after resection of functional neuroendocrine tumors: An 8‐institution study from the US Neuroendocrine Tumor Study Group-Reference-Cited by-同舟云学术

The impact of failure to achieve symptom control after resection of functional neuroendocrine tumors: An 8‐institution study from the US Neuroendocrine Tumor Study Group

Published:2018-11-27 Issue:1 Volume:119 Page:5-11
ISSN:0022-4790
Container-title:Journal of Surgical Oncology
language:en
Short-container-title:J Surg Oncol

Author:

Zaidi Mohammad Y.¹^ORCID,Lopez‐Aguiar Alexandra G.¹^ORCID,Poultsides George A.²,Dillhoff Mary³,Rocha Flavio G.⁴,Idrees Kamran⁵,Nathan Hari⁶,Winslow Emily R.⁷,Fields Ryan C.⁸,Cardona Kenneth¹^ORCID,Maithel Shishir K.¹,

Affiliation:

1. Division of Surgical OncologyDepartment of Surgery, Winship Cancer Institute, Emory UniversityAtlanta Georgia

2. Department of SurgeryStanford University Medical CenterStanford California

3. Division of Surgical OncologyThe Ohio State University Comprehensive Cancer CenterColumbus Ohio

4. Department of SurgeryVirginia Mason Medical CenterSeattle Washington

5. Division of Surgical OncologyDepartment of Surgery, Vanderbilt University Medical CenterNashville Tennessee

6. Division of Hepatopancreatobiliary and Advanced Gastrointestinal SurgeryDepartment of Surgery, University of MichiganAnn Arbor Michigan

7. Department of SurgeryUniversity of Wisconsin School of Medicine and Public HealthMadison Wisconsin

8. Department of SurgeryWashington University School of MedicineSt Louis Missouri

Publisher

Wiley

Subject

Oncology,General Medicine,Surgery

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/jso.25306

Reference28 articles.

1. Management of Pancreatic Neuroendocrine Tumors

2. Pancreatic neuroendocrine tumors: contemporary diagnosis and management

3. Clinical Presentation and Diagnosis of Pancreatic Neuroendocrine Tumors

4. Les insulinomes dans les néoplasies endocriniennes multiples de type 1 (NEM1). À propos d'une série de 44 cas du groupe d'étude des néoplasies endocriniennes multiples (GENEM)

5. Inherited pancreatic endocrine tumor syndromes: Advances in molecular pathogenesis, diagnosis, management, and controversies

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