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Blake's pouch cyst (BPC), or persistent Blake's pouch, is a condition that arises when Blake's pouch, an invagination in the fourth ventricle that ruptures at around 4 months of gestation to form the foramen of Magendie (medial aperture), fails to rupture. This can lead to a dilated fourth ventricle and subsequent hydrocephalus of all four ...
The cyst wall is composed of squamous epithelium (90%), columnar cells with or without cilia, or a mixture of both, with lymphoid infiltrate, often with prominent germinal centers and few subcapsular lymph sinuses. The cyst is typically surrounded by lymphoid tissue that has attenuated or absent overlying epithelium due to inflammatory changes.
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.
Rathke's pouch is a sac-like structure that gives rise to the pars distalis, pars intermedia, and pars tuberalis of the pituitary gland. The cells of Rathke's pouch proliferate and differentiate into various hormone-producing cells, including Somatotrophs, Lactotrophs, Corticotrophs, Thyrotrophs, and Gonadotrophs.
A thyroglossal cyst or thyroglossal duct cyst is a fibrous cyst that forms from a persistent thyroglossal duct. Thyroglossal cysts can be defined as an irregular neck mass or a lump which develops from cells and tissues left over after the formation of the thyroid gland during developmental stages.
Tornwaldt's disease is a rare benign disorder caused by persistent notochord remnants. [3] This disease almost remains asymptomatic. [citation needed] At about the 10th week of embryonic development, the pharyngeal pouch forms by adhesion of the pharyngeal ectoderm to the cranial end of the notochord.
[2]: 1062 About 10-15% of gastrointestinal stromal tumors (GISTs) carry wild-type sequences in all hot spots of KIT and platelet-derived growth factor receptor alpha (PDGFRA) (wt-GISTs). These tumors are currently defined by having no mutations in exons 9, 11, 13, and 17 of the KIT gene and exons 12, 14, and 18 of the PDGFRA gene.
Fundic gland polyposis is a medical syndrome where the fundus and the body of the stomach develop many fundic gland polyps.The condition has been described both in patients with familial adenomatous polyposis (FAP) and attenuated variants (AFAP), and in patients in whom it occurs sporadically.