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gastrinoma/proljev
Veza se sprema u međuspremnik
Stranica 1 iz 117 rezultatima
Acute kidney injury following vomiting and diarrhea after endoscopy in a duodenal gastrinoma patient.
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A 51-year-old woman complaining of weakness in the limbs was diagnosed as having a duodenal gastrinoma on performing a further evaluation. Surgical resection was performed with selective arterial calcium injection for localization. During preoperative hospitalization, she experienced recurrent
An uncommon cause of abdominal pain and diarrhea-gastrinoma in an adolescent.
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Gastrinoma is a hormone-secreting tumor associated with the Zollinger-Ellison syndrome. It is quite rare among children, and it is also uncommon in locations other than the pancreas and the duodenum in the pediatric group. Here, we describe an adolescent male, presenting with recurrent secretory
[PPI-sensitive diarrhea - unusual case of an adolescent with sporadic gastrinoma].
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METHODS
A 14-year-old boy was admitted to hospital because of chronic episodic diarrhea lasting for 4 years. Previous investigations in the past had not revealed the cause of the symptoms.
METHODS
The 13C-triglyceride breathing test showed a diminished intestinal lipolysis. Endoscopic examination
[Diarrhea as clinical expression of gastrinoma. A case report].
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We present a case of Zollinger Ellison Syndrome (ZES), that manifested itself as chronic diarrhea, without the presence of peptic ulcer disease. The purpose of this work in to report a case of ZES with and unusual clinical manifestation and to review the diagnostic methods (gastrin, secretin
Brief report: a duodenal gastrinoma in a patient with diarrhea and normal serum gastrin concentrations.
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[Case of Zollinger-Ellison syndrome caused by duodenal gastrinoma presenting as refractory diarrhea and originally diagnosed by endoscopy].
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[A case of Zollinger-Ellison syndrome due to duodenal gastrinoma with incurable diarrhea which was led to diagnosis by endoscopic examination].
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[A young man with chronic diarrhea and epigastric pain].
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METHODS
A 26-year-old man was admitted to hospital with a 6-month history of diarrhea and abdominal pain. Before admission, upper and lower gastrointestinal endoscopy had shown a mild erosive duodenitis and the patient was started on a proton pump inhibitor. Physical examination and laboratory tests
Diagnosis and treatment of gastrinoma in the era of proton pump inhibitors.
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The Zollinger-Ellison syndrome is characterized pathophysiologically by a significant hypergastrinemia derived from a gastrin-secreting neuroendocrine tumor with a primary location in the pancreas or duodenum. Chronic hypergastrinemia in turn triggers gastric acid hypersecretion yielding in chronic
The early diagnosis of gastrinoma.
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Despite the increasing awareness of gastrinoma and its lethal peptic ulcer sequelae, the diagnosis is often initially missed or made as a terminal event. The authors screened all patients with peptic ulcer symptoms serious enough to warrant hospital admission or those associated with diarrhea,
Hepatic gastrinoma.
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A solitary hepatic tumor in a 50-year-old woman, which was observed as a hemangioma, ultimately was resected because it increased in size. The tumor volume doubling time was 28.8 months over the observed period of 30 months. The histologic diagnosis was carcinoid tumor. Immunohistochemical staining
Clinical treatment of gastrinoma: A case report and review of the literature.
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Gastrinoma is a gastrin-secreting tumor that is associated with Zollinger-Ellison syndrome. The majority of cases occur in the pancreas, followed by the duodenum. Early diagnosis is difficult due to the relative rarity of the tumor and the lack of specific symptoms. In the current study, a
Gastrinoma and neurofibromatosis type 2: the first case report and review of the literature.
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BACKGROUND
Gastroenteropancreatic neuroendocrine tumors have occasionally been described in association with neurofibromatosis type 1, whereas an association with neurofibromatosis type 2 has never been reported.
METHODS
This report refers to an Italian 69 year old woman with neurofibromatosis type
Insulinoma and gastrinoma syndromes from a single intrapancreatic neuroendocrine tumor.
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BACKGROUND
The insulinoma syndrome is marked by fasting hypoglycemia and inappropriate elevations of insulin. The gastrinoma syndrome is characterized by hypergastrinemia, ulcer disease, and/or diarrhea. Rarely, insulinoma and gastrinoma coexist in the same patient simultaneously.
OBJECTIVE
Our
Lansoprazole: a cause of secretory diarrhea.
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A case of severe diarrhea and hypergastrinemia after 6 wk of lansoprazole therapy is presented. This represents the only fully evaluated report of severe diarrhea due to lansoprazole and comes to the interesting conclusion that it was a secretory diarrhea likely due to lansoprazole and not a
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