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Pyloric Obstruction01:11

Pyloric Obstruction

Pyloric obstruction, also referred to as gastric outlet obstruction, is a condition characterized by narrowing or blockage at the pylorus—the muscular valve regulating the flow of stomach contents into the duodenum. When this passage becomes impaired, the stomach cannot effectively empty its contents into the small intestine. This disruption leads to a range of gastrointestinal symptoms, including early satiety, bloating, epigastric pain, postprandial nausea, persistent vomiting, and...
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Oxytocin, produced in the hypothalamus and released by the pituitary gland, plays a role in social bonding, childbirth, and lactation.
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Cushing Syndrome II: Pathophysiology

Cortisol production is normally governed by the hypothalamic–pituitary–adrenal (HPA) axis, which maintains hormonal balance through tightly regulated feedback mechanisms. Disruption of this regulatory system is central to the development of Cushing syndrome, whether the excess cortisol originates from external medications or internal pathology. Persistent cortisol elevation alters metabolism, immune function, and endocrine signaling, producing the characteristic clinical features of the...
The Pituitary Gland01:17

The Pituitary Gland

The pituitary is a small endocrine organ in the sphenoid bone under the hypothalamus. Primarily, the pituitary in adults has two distinct anatomical and functional regions— the anterior and posterior lobes. During human fetal development, a third pituitary gland region called the pars intermedia atrophies and disappears. However, some of its cells migrate and exist adjacent to the anterior pituitary in adults.
Hypothyroidism II: Pathophysiology01:23

Hypothyroidism II: Pathophysiology

Hypothyroidism is a disorder characterized by insufficient production of thyroid hormones, which regulate metabolism, energy balance, and multiple organ systems.TypesHypothyroidism is classified based on the level of dysfunction. Primary hypothyroidism results from intrinsic thyroid gland dysfunction, causing reduced hormone production despite normal or increased stimulation. Secondary hypothyroidism arises from inadequate thyroid-stimulating hormone (TSH) secretion by the pituitary. Tertiary...
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The small, pea-sized pituitary gland is located at the base of the brain. It is crucial in regulating various bodily functions, from growth to reproduction. The gland is divided into the anterior lobe and the posterior lobe. The secretory cell clusters in the pars distalis of the anterior pituitary lobe are controlled by hypothalamic regulators and synthesize six primary hormones.
The most abundantly secreted hormone from the anterior lobe is the growth hormone, which controls overall growth by...

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Endoscopic Endonasal Trans-sphenoidal Approach: Minimally Invasive Surgery for Pituitary Adenomas
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Hyperprolactinaemia and the empty sella.

M Thwin1, B P Brophy

  • 1Department of Neurosurgery, Royal Adelaide Hospital, North Terrace, Adelaide, South Australia 5000, Australia. mthwin86@gmail.com

Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia
|January 17, 2012
PubMed
Summary
This summary is machine-generated.

Empty sella syndrome, a condition affecting the sella turcica, may be linked to hyperprolactinemia. This case report highlights a patient with elevated prolactin levels and empty sella diagnosed via MRI.

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Area of Science:

  • Endocrinology
  • Neuroimaging
  • Radiology

Background:

  • Hyperprolactinemia is an endocrine disorder characterized by elevated serum prolactin levels.
  • Empty sella is a radiological diagnosis of a deformed and enlarged sella turcica, often without intrinsic pituitary pathology.
  • The relationship between empty sella syndrome and hyperprolactinemia remains incompletely understood.

Observation:

  • A patient presented with symptoms of meningeal irritation and a history of galactorrhea.
  • The patient exhibited elevated serum prolactin levels.
  • Magnetic Resonance Imaging (MRI) confirmed the diagnosis of empty sella.

Findings:

  • The patient was diagnosed with hyperprolactinemia.
  • Empty sella syndrome was identified as a concurrent radiological finding.
  • The case suggests a potential association between these two conditions.

Implications:

  • Further research is warranted to elucidate the role of empty sella syndrome in the pathogenesis of hyperprolactinemia.
  • This case underscores the importance of considering endocrine evaluation in patients with empty sella.
  • Understanding this association may improve diagnostic and therapeutic strategies for patients with unexplained hyperprolactinemia.