Peutz Jeigher's Syndrome Essay

Peutz-Jeghers Syndrome is described by a Dutch physician named Jan Peutz back in 1921. Jan Peutz noted signs in a Dutch family appearing with intestinal polyps and also had noticed mucocutaneous macules. John McHutchinson, a man who reported signs in the year of 1896, had a case involving a pair of twins that was identical with an ending result leaving one twin that died. An American physician, Harold Jeghers, had published a statement with a definite descriptions of this syndrome. Shortly after that statement got published, it then became introduced as Peutz-Jeghers Syndrome by Andre J. Bruwer. Peutz-Jeghers Syndrome is a noncancerous developmental growth that should get recognized as early as possible to have a physical examination. Peutz-Jeghers Syndrome is also known as Hamartomatous Polyps. The polyps are found in the gastrointestinal tract (GI tract) and also in buccal mucosa. Children that are diagnosed with Peutz-Jeghers Syndrome start to appear with small and dark spots that are noticeable certain areas of the body. These spots are located on the lips, inside the mouth, and around the eyes. They can also appear around the nostril cavity and may even surround the anus. Peutz-Jeghers Syndrome has

Having periodic x-rays or endoscopy’s should start when the individual first becomes an adolescent and monitored throughout as an adult. When having Peutz-Jeghers Syndrome, follow-ups should be considerable by a family physician that is familiar with the individual’s condition and history. The physician should be taking notes and keeping an update on how the health of an individual with Peutz-Jeghers Syndrome is doing. When taking notes, any health concerns, procedure, or discussions with the individual should have be noted in the history of an individual with Peutz-Jeghers