{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2022,12,31]],"date-time":"2022-12-31T15:29:29Z","timestamp":1672500569977},"reference-count":33,"publisher":"FapUNIFESP (SciELO)","issue":"6","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Rev. Hosp. Clin."],"published-print":{"date-parts":[[2000,12]]},"abstract":"<jats:p>The Peutz-Jeghers syndrome is a hereditary disease that requires frequent endoscopic and surgical intervention, leading to secondary complications such as short bowel syndrome. CASE REPORT: This paper reports on a 15-year-old male patient with a family history of the disease, who underwent surgery for treatment of an intestinal occlusion due to a small intestine intussusception. DISCUSSION: An intra-operative fiberscopic procedure was included for the detection and treatment of numerous polyps distributed along the small intestine. Enterotomy was performed to treat only the larger polyps, therefore limiting the intestinal resection to smaller segments. The postoperative follow-up was uneventful. CONCLUSION: We point out the importance of conservative treatment for patients with this syndrome, especially those who will undergo repeated surgical interventions because of clinical manifestation while they are still young.<\/jats:p>","DOI":"10.1590\/s0041-87812000000600005","type":"journal-article","created":{"date-parts":[[2005,4,27]],"date-time":"2005-04-27T13:21:32Z","timestamp":1114608092000},"page":"219-224","source":"Crossref","is-referenced-by-count":3,"title":["Intestinal intussusception and occlusion caused by small bowel polyps in the Peutz-Jeghers syndrome. Management by combined intraoperative enteroscopy and resection through minimal enterostomy: case report"],"prefix":"10.1590","volume":"55","author":[{"given":"Joaquim J.","family":"Gama-Rodrigues","sequence":"first","affiliation":[{"name":"University of S\u00e3o Paulo"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Jos\u00e9 Hyppolito da","family":"Silva","sequence":"additional","affiliation":[{"name":"University of S\u00e3o Paulo"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Adilson A.","family":"Aisaka","sequence":"additional","affiliation":[{"name":"University of S\u00e3o Paulo"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Ricardo","family":"Jureidini","sequence":"additional","affiliation":[{"name":"University of S\u00e3o Paulo"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Renato","family":"Falci J\u00fanior","sequence":"additional","affiliation":[{"name":"University of S\u00e3o Paulo"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Fauze","family":"Maluf Filho","sequence":"additional","affiliation":[{"name":"University of S\u00e3o Paulo"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"A. Kim","family":"Chong","sequence":"additional","affiliation":[{"name":"University of S\u00e3o Paulo"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Andr\u00e9 Wan Wen","family":"Tsai","sequence":"additional","affiliation":[{"name":"University of S\u00e3o Paulo"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Cl\u00e1udio","family":"Bresciani","sequence":"additional","affiliation":[{"name":"University of S\u00e3o Paulo"}],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"530","reference":[{"issue":"7","key":"ref1","doi-asserted-by":"crossref","first-page":"182","DOI":"10.4314\/cajm.v45i7.8481","article-title":"Sporadic Peutz-Jeghers syndrome in a Nigerian","volume":"45","author":"ANYANWU SN","year":"1999","journal-title":"Cent Afr J Med","ISSN":"http:\/\/id.crossref.org\/issn\/0008-9176","issn-type":"print"},{"key":"ref2","doi-asserted-by":"crossref","first-page":"267","DOI":"10.1055\/s-2007-1005447","article-title":"Carcinoma in situ arising in a gastric hamartomatous polyp in a patient with Peutz-Jeghers syndrome","volume":"28","author":"BEYER AR","year":"1996","journal-title":"Endoscopy","ISSN":"http:\/\/id.crossref.org\/issn\/0013-726X","issn-type":"print"},{"issue":"1","key":"ref3","doi-asserted-by":"crossref","first-page":"1","DOI":"10.1002\/(SICI)1096-9896(199905)188:1<1::AID-PATH327>3.0.CO;2-J","article-title":"The hamartoma-adenoma-carcinoma sequence","volume":"188","author":"BOSMAN FT","year":"1999","journal-title":"J Pathol","ISSN":"http:\/\/id.crossref.org\/issn\/0022-3417","issn-type":"print"},{"issue":"1","key":"ref4","doi-asserted-by":"crossref","first-page":"2","DOI":"10.3346\/jkms.1999.14.1.2","article-title":"Peutz-Jeghers syndrome: a new understanding","volume":"14","author":"CHOI HS","year":"1999","journal-title":"J Korean Med Sci","ISSN":"http:\/\/id.crossref.org\/issn\/1011-8934","issn-type":"print"},{"key":"ref5","first-page":"1330","article-title":"A Case of Peutz-Jeghers syndrome with polyposis, extreme iron deficiency anemia, and hamartoma - adenoma transformation: management by combined surgical and endoscopic approach","volume":"90","author":"DE FACQ L","year":"1995","journal-title":"Am J Gastroenterol","ISSN":"http:\/\/id.crossref.org\/issn\/0002-9270","issn-type":"print"},{"issue":"26","key":"ref6","first-page":"661","article-title":"Molecular and phenotypic markers of hamartomatous polyposis syndrome in the gastrointestinal tract","volume":"46","author":"ENTIUS MM","year":"1999","journal-title":"Hepatogastroenterology","ISSN":"http:\/\/id.crossref.org\/issn\/0172-6390","issn-type":"print"},{"key":"ref7","first-page":"604","article-title":"Traitement des tumeurs du gr\u00eale du syndrome de Peutz-Jeghers: Int\u00e9r\u00eat d'une approche combin\u00e9e, endoscopique et chirurgicale. 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