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The pouch eventually loses its connection with the pharynx giving rise to the anterior pituitary. The anterior wall of Rathke's pouch proliferates, filling most of the pouch to form pars distalis and pars tuberalis. The posterior wall forms pars intermedia. In some organisms, the proliferating anterior wall does not fully occupy Rathke's pouch ...
A Rathke's cleft cyst is a benign growth on the pituitary gland in the brain, specifically a mucin-filled [1] cyst in the posterior portion of the anterior pituitary gland. [2] [3] It occurs when the Rathke's pouch does not develop properly and ranges in size from 2 to 40 mm in diameter.
The anterior pituitary (also called the adenohypophysis or pars anterior) is a major organ of the endocrine system.The anterior pituitary is the glandular, anterior lobe that together with the (posterior pituitary, or the neurohypophysis) makes up the pituitary gland (hypophysis) which, in humans, is located at the base of the brain, protruding off the bottom of the hypothalamus.
Craniopharyngioma is a rare, usually suprasellar [15] neoplasm, which may be cystic, that develops from nests of epithelium derived from Rathke's pouch. [16] [17] Rathke's pouch is an embryonic precursor of the anterior pituitary. [citation needed] Craniopharyngiomas are typically very slow-growing tumors.
The pituitary gland is formed within the rostral neural plate. The Rathke's pouch, a cavity of ectodermal cells of the oropharynx, forms between the fourth and fifth week of gestation [26] and upon full development, it gives rise to the anterior pituitary gland. [27] By seven weeks of gestation, the anterior pituitary vascular system begins to ...
It develops from a depression in the dorsal wall of the pharynx (stomal part) known as Rathke's pouch. The anterior pituitary contains several different types of cells [9] that synthesize and secrete hormones. Usually there is one type of cell for each major hormone formed in anterior pituitary. With special stains attached to high-affinity ...
Autoimmune hypophysitis can lead to deficiencies in one or more pituitary hormones, causing central diabetes insipidus if the posterior pituitary gland is affected as well as central adrenal insufficiency and central hypothyroidism if the anterior pituitary gland is affected. [1] The symptoms depend on what part of the pituitary is affected.
Most commonly, the initial symptoms are headaches and visual disturbances. Some symptoms are derived from the lesser functioning of the adenohypophyseal hormones. Of the adenohypophyseal hormones, the most frequently affected are corticotropes, lactotropes and gonadotropes, all which are found in the anterior pituitary.