Home
About Journal
Current Issue
Archive
Instructions
Editorial Board
Contact Us

        FULL TEXT
Submission
ToC     Instructions for Authors
APSP WEBSITE
IMAGES                                           APSP J Case Rep 2011; Vol. 2 (1)                             OPEN ACCESS



     Cecal Duplication Cyst Presenting as Acute Intestinal Obstruction in an Infant


                                                            Lubna Ijaz, Muhammad Husnain, Shahid Iqbal Malik, Bilal Mirza*

          Department of Paediatric Surgery, The Children's Hospital & The Institute of Child Health Lahore, Pakistan

                                                     *Corresponding Author's E-mail address:
blmirza@yahoo.com

                                                                                      
APSP J Case Rep 2011; 2: 11

                                                                           Competing Interest: None Declared



How to cite   

Ijaz L, Husnain M, Malik SI, Mirza B. Cecal duplication cyst presenting as acute intestinal obstruction in an infant. APSP J Case Rep 2011;2:11


A 45-day-old male infant presented with signs of acute intestinal obstruction for two days. Abdominal examination revealed a mass in the right lower abdomen. Ultrasound showed a cystic mass measuring 4x3 cm, in the right lower quadrant at the level of lower pole of right kidney. The plain abdominal radiograph showed haziness in the middle and lower third with bowel loops pushed to upper third of the abdomen (Fig. 1).

At operation, a cystic mass on the mesenteric side of the cecum was found. The small intestine was distended whereas large gut was collapsed (Fig. 2).  There was complete intestinal obstruction at the level of the cyst as appreciated by a failure of passage of the intestinal contents distally. The cystic mass was opened and about 50cc mucous drained. This resulted in sudden passage of intestinal contents into the ascending colon. The posterior wall of the cyst was being shared with the cecum. Mucosal stripping was performed after eversion.  Patient made an uneventful recovery and discharged home on 4th post-operative day. Histopathology confirmed it as cecal duplication.






PDF VERSION

H O M E  / I N S T R U C T I O N S  /  S U B M I S S I O N  /  C O N T A C T
Creative Commons License
DOAJ
Website developed by Bilal Mirza
search tips advanced search
site search by freefind
DISCUSSION

Duplications of the alimentary tract are rare anomalies. They may be of cystic or tubular variety with an intimate contact with the adjacent gut; smooth muscles in their wall and mucosa resemble that of intestine. Most common duplications occur along the ileum. Colonic duplications are rare (13%); cecal duplications are even rarer as only less than 20 cases have been reported in English literature [1-3].

They usually present within first two years of life in 80% of cases but has been reported in adults as well. Cecal duplications usually present with acute intestinal obstruction. They communicate with gut in less than 20% of cases where the presentation may be with bleeding per rectum if an ectopic gastric mucosa is present in it. Cecum is also a site where some colonic tubular duplications are intimately attached [1,2,3,5,6].

Ultrasound, CT scan, contrast bowel studies, technetium 99m radionuclide scan, and diagnostic laparoscopy are important tools for preoperative diagnosis; however, cecal duplications are diagnosed at operation in most of the cases. Our preoperative diagnosis was mesenteric cyst with a differential of alimentary tract duplication, not specifically of cecal origin.    

The mechanism of obstruction in case of cecal duplication depends upon the amount of mucous in its lumen. Fully loaded cecal duplication can obstruct the lumen of the normal cecum and may result in acute intestinal obstruction as in our case. Simple drainage of the mucus relieved obstruction in the index case.

Various surgical procedures have been employed to deal with such lesions. Cecal duplications are commonly managed by limited right hemicolectomy and ileocolic anastomosis [1-5]. In our case drainage of the mucous relieved obstruction therefore anterior wall was completely excised and mucosal stripping was performed on the common wall. The common wall appeared thin and redundant thus plicated along with the margins of the residual anterior wall of the duplication. 


REFERENCES

1. Keum S, Hwang M, Na J, Yu S, Kang D, Oh Y. Intestinal obstruction caused by duplication cyst of the cecum in a neonate. Korean J Pediatr 2009;52:261-4.

2. Lund DP. Alimentary tract duplications. In: O’Neill JA, Rowe MI, Grosfeld JL, Fonkalsrud WE, Coran AG. Editors. Pediatric Surgery, 6th ed, Philadelphia: Mosby, 2006:1389-99.

3. Oudshoorn JH, Heij HA. Intestinal obstruction caused by duplication of the cecum. Eur J Pediatr 1996; 155:338-40.

4. Shah A, Shah A. Diagnostic dilemma of cecal duplication. Indian Pediatrics 2004;41:749-50.

5. Martins JL, Cury ED, Petrilli AS, Martins ECS, Neto G. Cecal duplication causing disappearing abdominal mass in an infant. J Pediatr Surg 2001;36:1581-3.

6. Sharif M, Iqbal S, Mirza B, Ijaz L, Saleem M, Sheikh A. Atresia of colonic tubular duplication: a case report. [Online]. 2009 July 01 [cited 01-03-2011]; Available from: http://www.babysurgeon.com/pdf/Atresia-of-colonic-tubular-duplication.pdf

IMAGES