rntro Cystom. (lntestin;.il Duplications and , or intes-, SUtinal Cysts). These are . congenital cysts who contain wall has a same histologie pattern as intestinal wall, and they are common in ab- dominal cavity and 70% of them are located in ileocecal region. Twenty percent (20%)oi these cysts have a entrance to intestinal lumen and the rest of them are closed cysts. With duplications in thorax there are other abnormalities in vertebra1es of column which together make KlipelFeil. Syndrome, or we can discuss about other abnormality such as malrotation with these duplications. There are different hypothesis about the origin and development of these cysts that need further investigations.
In synptomatolo1ic section, different and a typical symptoms of duplications were discussed, and in addit io 11 of symptoms was their treatment which is always surgery.
Then there are reports about ten patients who have gastrointestinal duplicaton, which we discuss only three cases of them.
Th ese cases are:
1 · A woman with 28 year-a Id w h o ha s a Enterogenous cyst in terminal ileum.
2. An infant with 11 month of age (female) who has duodenum duplication.
3. A child with 2½ year-old (female) who has entero- genous cyst.
4. A child with 2 year-old (female) with small intestine duplication which has a entrance to main intestine (small intestine).
5. An infant with 5 month of age (male) who has enterogenous cyst.
6. A child with 13 year old ( male) who has a stomach duplication and within his stomach he has a ulcer which was perforated.
7. An infant with 3 month of age (female) who has a stomach duplication which again there was perforation of ulcer, and in additionsubphrenicabscesstlad formed.
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بین رشته ای ( مدیریت آموزشی، تحقیقات آموزشی، آموزش پزشکی ) دریافت: 1398/12/26 | پذیرش: 1398/12/26 | انتشار: 1398/12/26