Gastroschisis with multiple atresia and impending rupture of small intestine

We herein report an unusual case of multiple atresia and impending rupture of the small intestine in a patient with gastroschisis. Gradual bowel dilatation and thinning of the bowel wall were confirmed at our institution by fetal imaging, which led to the suspicion of intestinal atresia. The patient...

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Main Authors: Tsubasa Shironomae, Yutaka Hirayama, Yasushi Iinuma, Kyoko Morikawa, Hirotomo Nakahara, Koko Yoshida, Takumi Kurabayashi
Format: Article
Language:English
Published: Elsevier 2019-05-01
Series:Journal of Pediatric Surgery Case Reports
Online Access:http://www.sciencedirect.com/science/article/pii/S2213576619300387
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spelling doaj-583083b1794e4a8f9ebf58c635e50aca2020-11-25T00:52:54ZengElsevierJournal of Pediatric Surgery Case Reports2213-57662019-05-0144Gastroschisis with multiple atresia and impending rupture of small intestineTsubasa Shironomae0Yutaka Hirayama1Yasushi Iinuma2Kyoko Morikawa3Hirotomo Nakahara4Koko Yoshida5Takumi Kurabayashi6Departments of Pediatric Surgery, Niigata City General Hospital, 463-7 Shumoku, Chuo-ku, Niigata, Niigata 950-1197, Japan; Corresponding author. Department of Urology, Miyagi Children's Hospital, 4-3-17 Ochiai, Aoba-ku, Sendai, Miyagi 989-3126, Japan. Tel.: +81 22 391 5111; fax: +81 22 391 5116.Departments of Pediatric Surgery, Niigata City General Hospital, 463-7 Shumoku, Chuo-ku, Niigata, Niigata 950-1197, JapanDepartments of Pediatric Surgery, Niigata City General Hospital, 463-7 Shumoku, Chuo-ku, Niigata, Niigata 950-1197, JapanDepartment of Obstetrics and Gynecology, Niigata City General Hospital, 463-7 Shumoku, Chuo-ku, Niigata, Niigata 950-1197, JapanDepartments of Pediatric Surgery, Niigata City General Hospital, 463-7 Shumoku, Chuo-ku, Niigata, Niigata 950-1197, JapanDepartment of Diagnostic Pathology, Niigata City General Hospital, 463-7 Shumoku, Chuo-ku, Niigata, Niigata 950-1197, JapanDepartment of Obstetrics and Gynecology, Niigata City General Hospital, 463-7 Shumoku, Chuo-ku, Niigata, Niigata 950-1197, JapanWe herein report an unusual case of multiple atresia and impending rupture of the small intestine in a patient with gastroschisis. Gradual bowel dilatation and thinning of the bowel wall were confirmed at our institution by fetal imaging, which led to the suspicion of intestinal atresia. The patient underwent repair of the perforation and small intestinal resection, formation of a separate stoma, and primary closure of the abdominal wall defect. The specimen from the impending rupture of the small intestine showed partial absence of the mucosal and muscular layers on the antimesenteric side and irregular thickness of the lamina and tunica muscularis, including the non-dilated intestine. The vascular density was lower in the area with absence of the mucosal and muscular layers than in the area with normal layers. We speculate that the multiple small intestinal lesions resulted from chronic vascular stress and high intestinal internal pressure. Intestinal lesions in patients with gastroschisis cannot be excluded even when dramatic bowel distention and thickening are absent on prenatal ultrasonography. In cases of prenatally diagnosed gastroschisis, cesarean delivery should be performed as soon as possible to minimize the damage caused by intestinal lesions. Keywords: Gastroschisis, Intestinal atresia, Intestinal impending rupturehttp://www.sciencedirect.com/science/article/pii/S2213576619300387
collection DOAJ
language English
format Article
sources DOAJ
author Tsubasa Shironomae
Yutaka Hirayama
Yasushi Iinuma
Kyoko Morikawa
Hirotomo Nakahara
Koko Yoshida
Takumi Kurabayashi
spellingShingle Tsubasa Shironomae
Yutaka Hirayama
Yasushi Iinuma
Kyoko Morikawa
Hirotomo Nakahara
Koko Yoshida
Takumi Kurabayashi
Gastroschisis with multiple atresia and impending rupture of small intestine
Journal of Pediatric Surgery Case Reports
author_facet Tsubasa Shironomae
Yutaka Hirayama
Yasushi Iinuma
Kyoko Morikawa
Hirotomo Nakahara
Koko Yoshida
Takumi Kurabayashi
author_sort Tsubasa Shironomae
title Gastroschisis with multiple atresia and impending rupture of small intestine
title_short Gastroschisis with multiple atresia and impending rupture of small intestine
title_full Gastroschisis with multiple atresia and impending rupture of small intestine
title_fullStr Gastroschisis with multiple atresia and impending rupture of small intestine
title_full_unstemmed Gastroschisis with multiple atresia and impending rupture of small intestine
title_sort gastroschisis with multiple atresia and impending rupture of small intestine
publisher Elsevier
series Journal of Pediatric Surgery Case Reports
issn 2213-5766
publishDate 2019-05-01
description We herein report an unusual case of multiple atresia and impending rupture of the small intestine in a patient with gastroschisis. Gradual bowel dilatation and thinning of the bowel wall were confirmed at our institution by fetal imaging, which led to the suspicion of intestinal atresia. The patient underwent repair of the perforation and small intestinal resection, formation of a separate stoma, and primary closure of the abdominal wall defect. The specimen from the impending rupture of the small intestine showed partial absence of the mucosal and muscular layers on the antimesenteric side and irregular thickness of the lamina and tunica muscularis, including the non-dilated intestine. The vascular density was lower in the area with absence of the mucosal and muscular layers than in the area with normal layers. We speculate that the multiple small intestinal lesions resulted from chronic vascular stress and high intestinal internal pressure. Intestinal lesions in patients with gastroschisis cannot be excluded even when dramatic bowel distention and thickening are absent on prenatal ultrasonography. In cases of prenatally diagnosed gastroschisis, cesarean delivery should be performed as soon as possible to minimize the damage caused by intestinal lesions. Keywords: Gastroschisis, Intestinal atresia, Intestinal impending rupture
url http://www.sciencedirect.com/science/article/pii/S2213576619300387
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