scholarly journals SMALL BOWEL DIVERTICULOSIS WITH JEJUNAL ATRESIA

2015 ◽  
Vol 4 (56) ◽  
pp. 9849-9851
Author(s):  
Srinivas S ◽  
Ramesh Reddy K ◽  
Lavanya K
Keyword(s):  
2013 ◽  
Vol 79 (8) ◽  
pp. 826-828 ◽  
Author(s):  
Varun K. Bhalla ◽  
Walter L. Pipkin ◽  
Robyn M. Hatley ◽  
Charles G. Howell

The serial transverse enteroplasty procedure (STEP) was introduced as a bowel-lengthening procedure to reduce complications related to short bowel syndrome (SBS). Although some have described it as a useful adjunct to the Bianci procedure, others have acknowledged it as a primary procedure. We present a case of jejunal atresia in which two STEP procedures were performed 7 months apart to increase small bowel length. A 1-day-old, term girl presented with a known bowel obstruction diagnosed in utero. A laparotomy revealed a Type IIIb jejunal atresia with no remaining small bowel or cecum. A STEP procedure with an end jejunostomy and ascending colon mucous fistula lengthened the small bowel from 35 to 50 cm. A repeat procedure 7 months later lengthened it to 89 cm. The STEP procedure results in slower intestinal transit time and increases enterocytes contact with oral intake. We performed it during our initial exploration to increase small bowel size by 30 per cent. A repeat procedure 7 months later increased length to 89 cm. The use of multiple, staged STEP procedures avoided the need for bowel transplantation and long-term total parenteral nutrition dependence, demonstrating its effectiveness as a primary procedure for the surgical management of SBS.


PEDIATRICS ◽  
1960 ◽  
Vol 26 (1) ◽  
pp. 122-125
Author(s):  
L. R. Schultz ◽  
G. H. Lawrence

A report of a premature infant with multiple congenital diaphragms of jejunum, ileum, and rectum has been presented. The etiology and treatment have been reviewed. Barium enema preoperatively to establish patency of the colon in cases of congenital obstruction of the small bowel is recommended.


2013 ◽  
Vol 17 (1) ◽  
pp. 16-18 ◽  
Author(s):  
Anith Chacko ◽  
Farzanah Ismail ◽  
Sirajudeen Ellemdin

Agenesis of the dorsal mesentery is a rare occurrence that usually presents in children. It is associated with proximal small bowel malrotation as well as high jejunal atresia with discontinuity of the small bowel. We present a case report of an adolescent presenting with clinical features of proximal small bowel obstruction (confirmed on imaging) as well as acute pancreatitis. At laparotomy, he was found to have no dorsal mesentery, without small bowel atresia, and the duodenum was fixed to the posterior abdominal wall. The patient recovered well and remained symptom-free.


1972 ◽  
Vol 7 (4) ◽  
pp. 414-419 ◽  
Author(s):  
Gerald T. Zwiren ◽  
H. Gibbs Andrews ◽  
Peter Ahmann

2016 ◽  
Vol 5 (4) ◽  
pp. 65 ◽  
Author(s):  
R S Sisodiya ◽  
S S Panda ◽  
C K Gupta ◽  
S K Sinha
Keyword(s):  

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