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adenoma/vomiting

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Brunner's gland adenoma: a rare cause of vomiting.

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Upper gastrointestinal system adenoma is generally seen amongst elderly patients and quite rarely seen during the childhood. A 14-y-old female patient was referred to our hospital with complaints of vomiting and abdominal pain. She had been followed up for 6 y with the diagnosis of familial

A 70-year-old man with diplopia, nausea, and vomiting. Rathke cleft cyst concomitant with pituitary adenoma.

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Daily Cerebral Vomiting of Six Months' Duration Due to a Columnar-Celled Adenoma of the Cerebellum Involving the Fourth Ventricle.

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Ovarian Hyperstimulation Caused by Gonadotroph Pituitary Adenoma--Review.

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Ovarian hyperstimulation syndrome (OHSS) occurs mostly as an iatrogenic complication of assisted reproductive technology. Gonadotroph pituitary adenomas are rarely associated with OHSS. To the authors' knowledge, to date only 30 cases of spontaneous ovarian stimulation associated with gonadotroph

Two-stage liver transplant for ruptured hepatic adenoma: A case report.

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Only one case of liver transplantation for hepatic adenoma has previously been reported for patients with rupture and uncontrolled hemorrhage. We present the case of a massive ruptured hepatic adenoma with persistent hemorrhagic shock and toxic liver syndrome which resulted in a

Xanthogranulomatous pituitary adenoma: A case report and literature review.

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Xanthogranuloma, also referred to as cholesterol granuloma or xanthogranulomatous reaction, is a granulomatous lesion that is infrequently found in the sellar and parasellar regions. Xanthogranulomatous pituitary adenoma is relatively rare and, thus, the etiology, diagnosis, management and prognosis

Spontaneous intracranial hypotension with pituitary adenoma.

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Spontaneous intracranial hypotension (SIH) is an unusual syndrome that is characterised by positional headache, neck rigidity, nausea and vomiting. The characteristic magnetic resonance imaging (MRI) findings are diffuse smooth pachymeningeal thickening and enhancement, downward displacement of

Sudden Headache and Blindness Due to Pituitary (Adenoma) Infarction: A Case Report.

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Pituitary infarction (PI) is a rare medical emergency appearing in patients with pituitary adenoma, presenting with sudden onset of severe headache, and often associated with vomiting, nausea, visual deterioration, and decreased consciousness. We describe an 83-year-old woman who presented with

Spontaneous remission of acromegaly or gigantism due to subclinical apoplexy of pituitary growth hormone adenoma.

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BACKGROUND Subclinical apoplexy of pituitary functional adenoma can cause spontaneous remission of hormone hypersecretion. The typical presence of pituitary growth hormone (GH) adenoma is gigantism and/or acromegaly. We investigated the clinical characteristics of patients with spontaneous partial

Gestational Primary Hyperparathyroidism Due to Ectopic Parathyroid Adenoma: Case Report and Literature Review.

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Gestational primary hyperparathyroidism (GPHPT) is a rare condition with fewer than 200 cases reported. We present the case of a 21-year-old woman who presented at 10 weeks' gestation with severe hypercalcemia. Laboratory investigation was consistent with primary hyperparathyroidism. Neck ultrasound

Cecal perforation and adrenocortical adenoma in a dog.

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Cecal perforation was diagnosed in a dog with a history of acute vomiting. The dog also had an adrenocortical adenoma. Intestinal perforation can be a serious complication of cortico-steroid treatment in the dog, but has not been attributable to hyperadrenocorticism. Fever and an inflammatory CBC

[Quality of life in patients with pituitary adenomas in the pre- and postoperative period].

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To evaluate changes in quality of life in patients before and after the resection of pituitary adenoma.A clinical study involved 42 patients with pituitary adenomas. The diagnosis was based on clinical laboratory data, findings of radiology imaging and

[Adenoma of the Brunner's glands: a case report].

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We present a 84 year old male with a history of chronic diarrhea and megaloblastic anemia. A week before his hospitalization had nausea and vomit. An upper endoscopy showed a submucosa elevated lesion of 40 mm in the duodenum bulb, the biopsy was not contributory. The diarrhea and megaloblastic

[Pituitary apoplexy: retrospective study of 9 patients with hypophyseal adenoma].

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Pituitary apoplexy is an acute hemorrhage or ischemia infarction of the pituitary gland, almost invariably occurring in the presence of an pituitary adenoma. Although intratumoral bleeding occur in about 9.5 to 25% of pituitary adenomas, various series suggest that clinical apoplexy may be diagnosed

Pituitary apoplexy in an adolescent with prolactin-secreting adenoma.

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A 14.8-year-old girl was treated with bromocriptine for a prolactin-secreting adenoma. She suddenly developed headaches, vomiting, fever and meningeal syndrome. This was associated with corticotropin, thyrotropin and gonadotropin deficiencies. Magnetic resonance imaging showed peripheral enhancement
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