Results 11 to 20 of about 1,752 (196)

BYPASS-OMA: Hypoglycemic Hyperinsulinemic Nesidioblastosis after Gastric Bypass Surgery—A Case Report and Review of the Literature

open access: yesCase Reports in Endocrinology, 2022
This rare case vignette describes hypoglycemic, hyperinsulinemic nesidioblastosis in a female patient with prior Roux-en-Y gastric bypass. The patient presented with severe symptomatic hypoglycemia resistant to IV dextrose and diazoxide, requiring ...
Jessica Cao   +6 more
doaj   +2 more sources

Functional Localization of Adult-Onset Idiopathic Nesidioblastosis

open access: yesCase Reports in Endocrinology, 2022
Nesidioblastosis is a rare pancreatic disorder involving enlarged beta cells throughout the pancreas, causing elevated insulin production. We present the case of a 53-year-old woman with the initial symptom of fasting hypoglycemia.
Jess C. Hercus   +6 more
doaj   +2 more sources

Successful treatment of adult‐onset nesidioblastosis by continuous subcutaneous octreotide infusion in a patient on hemodialysis

open access: yesClinical Case Reports, 2021
Octreotide may be useful in noninsulinoma pancreatogenous hypoglycemia syndrome with nesidioblastosis patients who was on hemodialysis. Continuous octreotide subcutaneous infusion can reduce side‐effects and stabilize plasma glucose levels.
Rina Kato   +5 more
doaj   +2 more sources

An unusual cause of hypoglycemia in a middle-aged female after bariatric surgery [PDF]

open access: yesJournal of Community Hospital Internal Medicine Perspectives, 2014
Non-insulinoma pancreatogenous hypoglycemia syndrome (NIPHS) is a disorder characterized by postprandial hypoglycemia and islet cell hypertrophy. It is an uncommon complication of weight-loss surgery.
Ranjan Pathak   +3 more
doaj   +3 more sources

Hyperinsulinaemic hypoglycaemia - a diagnostic challenge. A report of two atypical cases. [PDF]

open access: yesEuropean Journal of Case Reports in Internal Medicine, 2015
Objectives: The authors describe 2 atypical cases of patients with hypoglycaemia, suspected for insulinoma. Methods: The 2 reports are accompanied by a concise review of the literature.
Renata Baronaite Hansen   +4 more
doaj   +5 more sources

Suspected congenital hyperinsulinism in a Shiba Inu dog

open access: yesJournal of Veterinary Internal Medicine, 2020
A 3‐month‐old male intact Shiba Inu dog was evaluated for a seizure disorder initially deemed idiopathic in origin. Seizure frequency remained unchanged despite therapeutic serum phenobarbital concentration and use of levetiracetam.
Simon Cook   +4 more
doaj   +2 more sources

Adult Nesidioblastosis in Chronic Kidney Disease

open access: yesCase Reports in Endocrinology, 2019
Context. Nesidioblastosis is a rare cause of hyperinsulinemic hypoglycemia in adults. The diagnosis is further complicated in patients with kidney failure, since impaired renal function can cause hypoglycemia by itself and diagnostic criteria for this ...
Eduardo Lozano-Melendez   +5 more
doaj   +2 more sources

Clinical Features and Causes of Endogenous Hyperinsulinemic Hypoglycemia in Korea [PDF]

open access: yesDiabetes & Metabolism Journal, 2015
BackgroundEndogenous hyperinsulinemic hypoglycemia (EHH) is characterized by an inappropriately high plasma insulin level, despite a low plasma glucose level. Most of the EHH cases are caused by insulinoma, whereas nesidioblastosis and insulin autoimmune
Chang-Yun Woo   +10 more
doaj   +1 more source

European Neuroendocrine Tumour Society (ENETS) 2023 guidance paper for nonfunctioning pancreatic neuroendocrine tumours

open access: yesJournal of Neuroendocrinology, Volume 35, Issue 12, December 2023., 2023
Abstract This ENETS guidance paper for well‐differentiated nonfunctioning pancreatic neuroendocrine tumours (NF‐Pan‐NET) has been developed by a multidisciplinary working group, and provides up‐to‐date and practical advice on the management of these tumours.
Beata Kos‐Kudła   +11 more
wiley   +1 more source

European Neuroendocrine Tumor Society 2023 guidance paper for functioning pancreatic neuroendocrine tumour syndromes

open access: yesJournal of Neuroendocrinology, Volume 35, Issue 8, August 2023., 2023
Abstract This ENETS guidance paper aims to provide practical advice to clinicians for the diagnosis, treatment and follow‐up of functioning syndromes in pancreatic neuroendocrine tumours (NET). A NET‐associated functioning syndrome is defined by the presence of a clinical syndrome combined with biochemical evidence of inappropriately elevated hormonal ...
Johannes Hofland   +35 more
wiley   +1 more source

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