Intestinal intussusception in Peutz Jeghers syndrome: A case report
نویسندگان
چکیده
منابع مشابه
Peutz-Jeghers syndrome, case report.
Peutz-Jeghers syndrome (PJS) is an unusual hamartomatous polyposis of the gastro intestinal (GI) tract, with pigmentation around lips and macules on the buccal mucosa. The case of a 10-year-old girl who presented with intussusception is reported. A polyp was found to be the cause of an invagination. Histologically it was a hamartoma. PJS is a rare syndrome inherited in an autosomal dominant pat...
متن کاملLaparoscopic treatment of intestinal intussusception in Peutz-Jeghers syndrome: case report and review of literature.
A 47-year-old woman presented with an abdominal mass and nausea. Abdominal ultrasound and computed tomography (CT) showed a sausage-shaped mass with invagination. One polyp that appeared to exceed 3 cm was found in the sigmoid colon. Laparoscopy confirmed an intussusception mass, and the intussusception was dissected by hand-assisted laparoscopy (HALS). The sigmoid colon was also mobilized to t...
متن کاملThe Peutz Jeghers Syndrome: A Case Report
Peutz Jeghers syndrome ( PJ S ) is an autosomal dominant disease that combines hamartomatous polyposis ,a periorificial lentiginose and a high risk of associated cancers. We report the observation of a girl 07 years old of personal historyof acute intestinal intussusception occurred a year ago who consults for signs of early puberty and the onset of vaginal bleeding up to 06 months . The child ...
متن کاملPeutz-Jeghers' Syndrome. A case report.
Peutz-Jeghers syndrome (PJS) is an unusual hamartomatous polyposis of the gastro intestinal (GI) tract, with pigmentation around lips and macules on the buccal mucosa. The case of a 10-year-old girl who presented with intussusception is reported. A polyp was found to be the cause of an invagination. Histologically it was a hamartoma. PJS is a rare syndrome inherited in an autosomal dominant pat...
متن کاملIntussusception secundary to Peutz-Jeghers syndrome
El síndrome de Peutz-Jeghers es una condición familiar caracterizada por la presencia de manchas cutáneas hiperpigmentadas y poliposis intestinal. La invaginación intestinal es la complicación abdominal más frecuente, pero es muy rara. Éste es el segundo reporte que se comunica en nuestro país. En este artículo presentamos cuatro pacientes que sufrieron el síndrome, que se complicó con invagina...
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ژورنال
عنوان ژورنال: Annals of Medicine and Surgery
سال: 2020
ISSN: 2049-0801
DOI: 10.1016/j.amsu.2020.04.013