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      Blowhole tangential cecostomy and transanal tube insertion for neonatal cecal perforation in a patient with Hirschsprung’s disease in the earlier definitive operation era

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          Abstract

          Background

          Although uncommon and seldom experienced, intestinal perforation is a well-known complication of Hirschsprung’s disease (HD). A literature review revealed that the cecum, including the appendiceal base, is a site of perforation. The cecum is not suitable for making an ordinary loop colostomy, and the optimal operative strategy remains to be established.

          Case presentation

          We present a combination technique composed of tangential cecostomy at the perforated portion and postoperative care with a transanal indwelling tube, which was used in the treatment of a 3-day-old boy with cecal perforation with long-segment Hirschsprung’s disease. A temporary simple blowhole stoma and continuous decompression with daily irrigation via a transanal indwelling tube in the distal colon achieved a secure recovery and was followed by a definitive operation in the early period. The combination of tangential cecostomy and transanal indwelling catheter management led to the preservation of the ileocecal valve.

          Conclusions

          We review the Japanese literature and emphasize the usefulness of this combination technique by blowhole tangential cecostomy and transanal tube insertion for neonatal cecal perforation in patients with HD in today’s early definitive operation era.

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          Most cited references11

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          Transanal endorectal pull-through for Hirschsprung's disease.

          A new endorectal pull-through technique using a transanal approach is presented in this report. Mucosectomy, colectomy, and pull-through are performed transanally, and neither laparotomy or laparoscopy are required. Five patients affected with Hirschsprung's disease have been operated on with this technique. During the 6- to 15-month follow-up period, all of them have had postoperative normal bowel movements.
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            Primary laparoscopic pull-through for Hirschsprung's disease in infants and children.

            Between November 1993 and September 1994, 12 primary laparoscopic colon pull-through procedures were performed in infants and children. The patients' ages ranged from 3 days to 6 years. The primary diagnosis in all 12 patients was Hirschsprung's disease. All children had their operations without construction of preoperative or postoperative colostomy. Three 5-mm abdominal wall ports were used for access to the peritoneal cavity. The sigmoid colon and proximal rectum were mobilized laparoscopically. A submucosal sleeve was developed transanally to meet the dissection from above. The colon was then pulled down in continuity, divided above the transition zone, and secured to the anal mucosa 5 to 10 mm above the pectinate line. Mean postoperative stay was 4 days. Laparoscopic visualization provides clear delineation of pelvic structures even in small infants. Laparoscopic pull-through requires no more time than similar open procedures, averaging just over 2 hours. The morbidities associated with colostomy formation and closure and the inconvenience of colostomy care are avoided with a one-stage technique. These benefits combined with the advantages of minimally invasive surgery make primary laparoscopic pull-through a potential advance in the surgical treatment of Hirschsprung's disease.
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              • Article: not found

              Diagnosis of congenital megacolon: an analysis of 501 patients.

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                Author and article information

                Contributors
                +81-92-801-1011 , shiraitk@fukuoka-u.ac.jp
                rhirose@fukuoka-u.ac.jp
                wispcloud@yahoo.co.jp
                inatomikaori@gmail.com
                y-yanag@pedsurg.med.kyushu-u.ac.jp
                iwanaka@pedsurg.med.kyushu-u.ac.jp
                akinori@fukuoka-u.ac.jp
                Journal
                Surg Case Rep
                Surg Case Rep
                Surgical Case Reports
                Springer Berlin Heidelberg (Berlin/Heidelberg )
                2198-7793
                10 July 2019
                10 July 2019
                December 2019
                : 5
                : 111
                Affiliations
                [1 ]ISNI 0000 0001 0672 2176, GRID grid.411497.e, Department of General Thoracic, Breast and Pediatric Surgery, Faculty of Medicine, , Fukuoka University, ; 7-45-1 Nanakuma, Jonan-ku, Fukuoka, Fukuoka 814-0180 Japan
                [2 ]GRID grid.415613.4, Department of Pediatric surgery, , National Kyushu Medical Center, ; 1-8-1 Jigyohama, Chuo-ku, Fukuoka, Fukuoka 810-8563 Japan
                Author information
                http://orcid.org/0000-0002-4418-6498
                Article
                667
                10.1186/s40792-019-0667-9
                6620225
                31292778
                948e4f51-0657-4b5a-ac3f-7fc15332f47f
                © The Author(s). 2019

                Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License ( http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.

                History
                : 28 May 2019
                : 1 July 2019
                Categories
                Case Report
                Custom metadata
                © The Author(s) 2019

                tangential cecostomy,neonatal intestinal perforation,hirschsprung’s disease,transanal indwelling tube

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