Intrauterine intussusception: a rare cause of intestinal atresia

2009 ◽  
Vol 44 (10) ◽  
pp. 2028-2030 ◽  
Author(s):  
Carlos Pueyo ◽  
Joaquín Maldonado ◽  
Yolanda Royo ◽  
Robert Skrabski ◽  
Ida Di Crosta ◽  
...  
Author(s):  
Khalilah Alhuda Binti Kamilen ◽  
Mohd Yusran Othman

Intussusception is a well-known cause of intestinal obstruction in children. Its occurrence in fetus as an intrauterine incidence is extremely rare and poses a diagnostic difficulty. Intrauterine intussusception may result in intestinal atresia once the gangrenous segment resorbed. However, a very late occurrence of intussusception just prior to delivery may present as meconium peritonitis. We are reporting a case of premature baby who was born at 35 weeks gestation via emergency caesarean for breech in labour. Routine scan 4 days prior to the delivery showed evidence of fetal ascites. She was born with good Apgar Score and weighed 2.5kg. Subsequently she developed respiratory distress syndrome requiring mechanical ventilation. She passed minimal meconium once after birth then developed progressive abdominal distension and vomiting. Abdominal radiograph on day 4 of life revealed gross pneumoperitoneum and bedside percutaneous drain was inserted to ease the ventilation. Upon exploratory laparotomy, a single ileal perforation was seen 20cm from ileocecal junction with an intussusceptum was seen in the distal bowel. Gross meconium contamination and bowel edema did not favour the option of primary anastomosis, thus stoma was created. Reversal of stoma was performed a month later and she recovered well. Fetus with a complicated intrauterine intussusception may present with fetal ascites and their postnatal clinical and radiological findings need to be carefully assessed for evidence of meconium peritonitis; in which a timely surgical intervention is required to prevent the sequelae of prolonged intraabdominal sepsis in this premature baby.International Journal of Human and Health Sciences Supplementary Issue-2: 2021 Page: S18


1999 ◽  
Vol 49 (11) ◽  
pp. 962-967 ◽  
Author(s):  
Yukihiro Imai ◽  
Eiji Nishijima ◽  
Toshihiro Muraji ◽  
Kimio Hashimoto ◽  
Yoshitake Hayashi ◽  
...  

1990 ◽  
Vol 25 (5) ◽  
pp. 562-563 ◽  
Author(s):  
O. Adejuyigbe ◽  
W.O. Odesanmi

2014 ◽  
Vol 2 (4) ◽  
pp. 203-205
Author(s):  
Taieb Chouikh ◽  
Awatef Charieg ◽  
Chaima Mrad ◽  
Sofiene Ghorbel ◽  
Sofiene Saada ◽  
...  

1975 ◽  
Vol 10 (4) ◽  
pp. 445-451 ◽  
Author(s):  
Takuji Todani ◽  
Katsusuke Tabuchi ◽  
Sanae Tanaka

2019 ◽  
Vol 15 (02) ◽  
pp. 81-82
Author(s):  
Madan Pal ◽  
Kashi Ram ◽  
Chander Pal Garhwal ◽  
Virender .

Atresia ani is a congenital defect that describes the absence of a normal anal opening. It is fatal unless a surgical correction is carried out to provide an anal opening. In female, the rectum may break through the vagina, forming a rectovaginal fistula permitting defecation via the vulva. Surgical treatment of atresia ani is indicated to save the animal’s life and to improve body weight gain. Intestinal atresia has been reported as a congenital defect in all species of domestic animals (Gass and Tibboel, 1980). Atresia ani may be caused by genetic disorders (chromosomes or transgenesis), environmental factors, or a combination of both (Cassini et al., 2005). Monsang et al. (2011) reported a case of double vulva with atresia ani in a crossbred calf. Atresia ani should be treated by a surgical operation to solve the problem, improve body weight gain, and reduce economic loss. The present report records a case of atresia ani in a crossbred cow-calf and its successful surgical correction.


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