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A Case of Zollinger-Ellison Syndrome with Gastrinoma Localized by 111In-Pentetreotide Scan

Jeong HJ, Ryu JS, Kim JS, Moon DH, Jung HY, Ha HK, Lee HK

  • KMID: 2038082
  • Korean J Nucl Med.
  • 1999 Dec;33(6):537-542.
In patient with Zollinger-Ellison syndrome, it is difficult to localize gastrinoma because the tumor is frequently small and multiple. However, accurate localization of the tumor is important for the treatment....
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A case of Zollinger-Ellison syndrome: localization of gastrinoma by selective intra-arterial calcium injection

Song HS, Jeong JJ, Song KS, Jeon EJ, Jie BS, Chun YJ, Choi SW

  • KMID: 2256415
  • Korean J Med.
  • 2007 May;72(5):529-535.
Zollinger-Ellison syndrome is a very rare disease that's caused by tumor having gastrin-producing cells, and this is accompanied by hypergastrinemia leading to gastric acid hypersecretion, peptic ulcer and their complications....
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A Case of Metachronous Multiple Endocrine Neoplasia Type I Manifested as Zollinger-Ellison Syndrome

Lee YM, Jung HY, Choi SY, Kang HH, Myung SJ, Yang SK, Hong WS, Kim JH, Min YI

  • KMID: 1606511
  • Korean J Gastroenterol.
  • 2002 Jan;39(1):50-54.
Zollinger-Ellison syndrome (ZES) is characterized by recurrent peptic ulcer and diarrhea caused by gastric acid hypersecretion due to gastrinoma. Approximately, one third of patients with gastrinoma have multiple endocrine neoplasia...
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A Case of Zollinger-Ellison Syndrome Caused by Gastrinoma Found in a Pyloric Region

Oh TH, Jung HY, Lee DH, Song HK, Kang SJ, Myung SJ, Yang SK, Hong WS, Kim JH, Min YI

  • KMID: 1865521
  • Korean J Gastrointest Endosc.
  • 2001 Dec;23(6):483-488.
Zollinger-Ellison syndrome (ZES) is characterized by severe peptic ulcer disease that results from gastrin-secreting tumors (gastrinoma) of the gastrointestinal tract. About 25% of patients have multiple endocrine neoplasia type 1...
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Synchronous Peripancreatic Lymph Node Gastrinoma and Gastric Neuroendocrine Tumor Type 2

Lee HW, Chung JW, Kim YJ, Kwon KA, Kim EJ, Kim KK, Lee WK, Sym SJ

A 34-year-old man was referred to our hospital with gastric polypoid lesions and biopsy-confirmed neuroendocrine tumor (NET). Computed tomography (CT) revealed a 3×3.5×8-cm retroperitoneal mass behind the pancreas, with multiple...
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A case of Zollinger-Ellison syndrome with MEN-1

Kong YH, Kim YD, Han KH, Lee SH, Jung WJ, Jang HJ, Cheon GJ

  • KMID: 2259099
  • Korean J Med.
  • 2010 Sep;79(3):289-294.
Zollinger-Ellison syndrome (ZES) is a clinical syndrome caused by excessive gastric acid secretion by gastrinoma, characteristically causing peptic disease and/or gastroesophageal reflux disease. Approximately one third of patients with gastrinoma...
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A Case of Zollinger-Ellison Syndrome in Multiple Endocrine Neoplasia Type 1 with Urolithiasis as the Initial Presentation

Lee NE, Lee YJ, Yun SH, Lee JU, Park MS, Kim JK, Kim JW, Cho JW

Zollinger-Ellison syndrome (ZES) is characterized by gastrinoma and resultant hypergastrinemia, which leads to recurrent peptic ulcers. Because gastrinoma is the most common pancreatic endocrine tumor seen in multiple endocrine neoplasia...
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Surgical Experiences of Functioning Neuroendocrine Neoplasm of the Pancreas

Kang CM, Park SH, Kim KS, Choi JS, Lee WJ, Kim BR

We present our surgical experiences with functioning neuroendocrine neoplasms of the pancreas to define its natural history, and to suggest its proper management. From June 1990 to June 2005, patients...
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A Case of Multiple Endocrine Neoplasia Type 1 with Papillary Thyroid Carcinoma

Kim HJ, Kim CS, Je HC, Park J, Park JS, Kong JH, Kang ES, Ahn CW, Cha BS, Lim SK, Kim KR, Lee HC, Jang HS, Hong SW

This is the first report of papillary thyroid carcinoma combined with multiple endocrine neoplasia type 1 (MEN 1). It is an hereditary syndrome characterized by neoplastic disorders such as pituitary...
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Refractory Peptic Ulcer Disease

Lim H

The eradication of Helicobacter pylori and the widespread use of effective antisecretory therapies, including proton pump inhibitors, have improved the management of peptic ulcer disease. However, in some patients, peptic...
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A Case of Multiple Endocrine Neoplasia Type 1 in Type 2 Diabetes Mellitus with Poor Glycemic Control

Lee YH, Lee YC, Lee JE, Lee SJ, Jeong SJ, Kim CH

The primary causes of uncontrolled diabetes are poor life-style, infection, ischemic heart disease and inappropriate usage of oral anti-diabetic agents and insulin. Supplementary causes are stroke, acute pancreatitis and endocrine...
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Clinical and Immunohistochemical Characteristics of Pancreatic Neuroendocrine Tumor: Immunohistochemical Analysis of 7 Tumors

Lee SM, Sohn CY, Kang KJ, Lim TJ, Cho SJ

  • KMID: 2095551
  • J Korean Surg Soc.
  • 1999 Jan;56(1):117-125.
BACKGROUND: Neuroendocrine tumors of the pancreas are classified according to the endocrine function as insulinomas gastrinomas somatostatinomas, or nonfunctioning tumors. However, the morphologic features are not different from each other....
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Clinical Manifestation of Multiple Endocrine Neoplasia Type I

Kim YS, Hong SJ

PURPOSE: Multiple endocrine neoplasia type I is rarely reported in Korea. The purpose of this study is to analyze the clinical features and the treatment of MEN1 which had been...
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Islet Cell Tumors of the Pancreas

Jung JP, Kim SC, Kim TH, Jang HJ, Han DJ

  • KMID: 2209292
  • J Korean Surg Soc.
  • 2000 Jun;58(6):840-850.
PURPOSE: Islet cell tumors are a rare disease that can be cured by surgical management if they are early diagnosed. However, diagnosis and localization are difficult due to their small...
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Incidental Detection of Parathyroid Adenoma on Somatostatin Receptor PET/CT and Incremental Role of ¹⁸F-Fluorocholine PET/CT in MEN1 Syndrome

Arora S, Damle NA, Passah A, Yadav MP, Ballal S, Aggarwal V, Gupta Y, Kumar P, Tripathi M, Bal C

Multiple endocrine neoplasia type 1 (MEN1) syndrome is characterized by combined occurrence of tumors of endocrine glands including the parathyroid, the pancreatic islet cells, and the anterior pituitary gland. Parathyroid...
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A Case of Familial Multiple Endocrine Neoplasia Type 1 with a Novel Mutation in the MEN1 Gene

Kim MJ, Kim EH, Shin MS, Kim JH, Na HK, Park SJ, Lee SA, Koh EH, Lee WJ, Song KH, Park JY, Lee KU, Kim GH, Yoo HW, Kim MS

Multiple endocrine neoplasia type 1 (MEN1) is an autosomal dominant disorder characterized by the occurrence of multiple tumors in the parathyroid gland, pancreatic islet, and pituitary gland. This condition is...
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Somatostatinoma of the Ampulla of Vater

Lee HW, Kim HC, Song OP, Lim CW, Shin EJ, Cho GS, Chu CW, Ko ES, Kwon KW, Hong SJ

  • KMID: 2325029
  • J Korean Surg Soc.
  • 2004 Mar;66(3):251-255.
Somatostatinoma is a rare form of neuroendocrine tumor that was first described in 1977. Most tumors have involved the pancreas, and gastrointestinal tract involvement is rare. Somatostatinomas of the ampulla...
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Experiences of Endoscopic Ultrasonography in the 5 cases with Pancreatic Insulinoma

Min YI, Lee SK, Kim MH, Kim HR, Song IH, Koh MS, Choi HS, Park JY, Hong SK, Lee KU, Seo DJ

  • KMID: 1929106
  • Korean J Gastrointest Endosc.
  • 1996 Feb;16(1):103-113.
Of the various endocrine tumors affecting the pancreas, insulinomas and gastrinomas are the most common. In order to facilitate surgery, the localization of tumor is important. However, at the first...
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Recent Update of Radiologic Findings and Interventional Methods of Pancreas Endocrine Tumor

Kim JW, Jeong YY

  • KMID: 2258968
  • Korean J Med.
  • 2011 Apr;80(4):378-385.
Pancreatic endocrine tumors (PET) are rare neoplasms of the pancreas accounting for less than 5% of all primary pancreatic malignancies. Insulinomas, gastrinomas, glucagonomas and somatostatinomas is included in PET. PETs...
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A Case of a Cutaneous Metastasis from an Endocrine Pancreatic Carcinoma

Kwon HB, Lee JH, Choi YS, Lee AY, Lee SH, Choi JS

  • KMID: 2247902
  • Korean J Dermatol.
  • 2009 May;47(5):592-595.
Pancreatic endocrine tumors (PET) are rare neoplasms of the pancreas and account for less than 5% of all primary pancreatic malignancies. Included in this group are insulinomas, gastrinomas, glucagonomas and...
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