Pharyngeal pouch: Difference between revisions
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Latest revision as of 22:36, 17 March 2025
Pharyngeal pouch
A pharyngeal pouch is a congenital anomaly that occurs in the pharynx, the part of the throat situated immediately behind the nasal cavity, behind the mouth, and above the esophagus and larynx. Pharyngeal pouches are outpouchings of the pharyngeal wall that can lead to various clinical symptoms depending on their size and location.
Anatomy and Development[edit]
Pharyngeal pouches are part of the pharyngeal apparatus, which also includes the pharyngeal arches and pharyngeal clefts. During embryonic development, the pharyngeal apparatus plays a crucial role in the formation of the head and neck structures. There are typically four pairs of pharyngeal pouches in humans, each contributing to different anatomical structures.
- The first pharyngeal pouch forms the middle ear cavity and the Eustachian tube.
- The second pharyngeal pouch gives rise to the palatine tonsils.
- The third pharyngeal pouch develops into the inferior parathyroid glands and the thymus.
- The fourth pharyngeal pouch forms the superior parathyroid glands and the ultimobranchial body, which contributes to the thyroid gland.
Clinical Significance[edit]
Pharyngeal pouches can sometimes persist abnormally, leading to conditions such as Zenker's diverticulum, which is a pouch that forms at the junction of the pharynx and the esophagus. Symptoms of a pharyngeal pouch may include dysphagia (difficulty swallowing), regurgitation of undigested food, chronic cough, and aspiration.
Diagnosis and Treatment[edit]
Diagnosis of a pharyngeal pouch typically involves imaging studies such as a barium swallow X-ray, which can reveal the presence of the pouch. Endoscopy may also be used to visualize the pouch directly. Treatment often involves surgical intervention to remove or reduce the size of the pouch, thereby alleviating symptoms.
Related Pages[edit]
Categories[edit]
| Congenital malformations and deformations of digestive system | ||||||||||||||
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