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LETTER TO THE EDITOR
APSP J Case Rep 2011; Vol. 2 (1)
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Recurrent Intussusception: Management
Options
Bilal
Mirza
Department of
Paediatric Surgery, The Children's Hospital & The Institute of Child Health
Lahore, Pakistan
E-mail
address: blmirza@yahoo.com
APSP J Case Rep 2011; 2: 9
Competing Interest: None Declared
How to cite
Mirza B. Recurrent
intussusception: management options. APSP J Case Rep 2011;2:9
Dear
Sir
Intussusception is referred to as recurrent when after being
spontaneously reduced it is re-diagnosed clinically and on ultrasound, later
confirmed at operation; or it is a post-operative intussusception in a patient
where it was reduced at an open surgery or non-operatively either with
hydrostatic or pneumatic method. [1-3].
Most of the recurrent
intussusceptions present within 6 months of initial episode and have been
observed with almost all the treatment modalities. These are frequently reported
after non-operative reduction (hydrostatic/pneumatic), whereas their incidence
is negligible after operative management. This is especially true where the
resection of the involved part of intestine is performed. The recurrence may
occur once to as many as 8 times or more [1-3].
There is ongoing debate
as to the management of recurrence. The recommended management is non-operative
reduction, however, a significant number of recurrent intussusceptions do have
pathological leads point (PLP); therefore operative management is required in
these cases [1]. The purpose of this letter is to discuss various management
options available for the treatment of recurrent intussusceptions based upon an
experience of three cases of recurrent intussusception.
Case 1:
A 3-month-old male infant presented with abdominal pain, two episodes of
bilious vomiting, irritability, and passage of currant jelly stool for two days.
There was a preceding history of diarrhea. Clinically a sausage shaped mass was
present in the lower abdomen. Ultrasound of the abdomen confirmed it as
intussusception. At operation, no intussusception was found and appeared to be
spontaneously reduced as indicated by hyperemia of a portion of distal ileum and
collapse of the ileum distal to edematous segment.
On the third
post-operative day the infant again developed similar features with toxic
features. Patient underwent re-operation and resection of gangrenous ileum with
primary end to end ileo-ileal anastomosis performed for ileo-ileal
intussusception. This time, the
Post-operative course remained uneventful.
There was no recurrence during a follow up of 15 months.
Case 2: A
6-m-old male infant presented with abdominal pain, vomiting, and passage of
currant jelly stool. The sausage shaped mass was palpable in the right upper
quadrant. Ultrasound abdomen also revealed a positive pseudo-kidney sign. At
operation ileo-colic intussusception found that was reduced manually. No PLP was
detected. On 4th post operative day the clinical features of
intestinal obstruction appeared. A diagnosis of recurrent intussusceptions was
made and hydrostatic reduction with saline enema under ultrasound guidance was
attempted. The intussusception was successfully reduced and the post-operative
course remained uneventful. The patient had no further recurrence and doing well
at 18 months of follow up.
Case 3: A 7-year-old boy presented
with colicky abdominal pain, bilious vomiting, and bleeding per rectum for 3
days. There was no history of any preceding illness. Ultrasound done a day
earlier suggested intussusception as suspected on clinical examination which
revealed a sausage shaped mass in the right iliac and lumbar regions. The mass
was spontaneously reduced within an hour of admission to our hospital. The
symptoms again developed on the next day with the mass detectable clinically and
demonstrated on ultrasound. The patient was planned for exploratory laparotomy
with a strong suspicion of PLP. On operation table under general anesthesia the
mass was not palpable. It was decided to proceed with laparotomy. Operative
signs of spontaneous reduction of ileo-colic intussusception were found but no
PLP demonstrated. Appendectomy was added with a view of probable PLP. The post
operative course was uneventful. The patient remained asymptomatic at 3 months
follow up.
The incidence of recurrent intussusceptions is 8-15% in most
of the big series. The recurrence is higher with hydrostatic and pneumatic
reduction (10-15%) and lower with operative reduction (1-3%). Post operative
adhesions play a vital role in preventing recurrence. The recurrence is almost
nil after resection of the involved portion of intestine which indicates that
the involved part of intestine, even in absence of an obvious PLP, has a key
role in development of recurrence [2].
Niramis et al have reported that
about 70% of patients with recurrent intussusceptions were infants with a
maximum incidence within 6 months of the initial episode. Frequently recurrent
intussusceptions may have PLP as a cause of recurrence. Previously we have
reported a case of recurrent colocolic intussusception in a 10 year old boy
having inflammatory fibroid polyp as a PLP. In contrary to that, Niramis et al
found maximum of 5 recurrences in two of their patients but neither of them had
PLP when explored for it [1,4].
The management of recurrent
intussusception is somewhat tricky. One cannot exactly anticipate the future
episodes of recurrences. Many authors are in favor of operative interventions in
case of more than one episodes of recurrence in patients older than 2 years. As
the recurrence is also reported after operative reduction therefore some authors
recommend ileocolopexy for prevention of recurrence however others do not
recommend it. Some authors suggested resection of involved portion of intestine
in case of multiple recurrences [1,5,6].
In summary, recurrent
intussusceptions may pose difficulties as to the management. The selection of
the treatment modality should be individualized as per case requirement.
Website developed by Bilal Mirza
REFERENCES
1. Niramis R, Watanatittan S, Kruatrachue A,
Anuntkosol M, Buranakitjaroen V, Rattanasuwan T, et al. Management of recurrent
intussusception: nonoperative or operative reduction? J Pediatr Surg
2010;45:2175-80.
2. Ein SH, Daneman A. Intussusception. In: O’Neill JA
Jr, Rowe MI, Grosfeld JL, et al, editors. Pediatric Surgery,
6th ed. Chicago: Year Book; 2006. p.1313-7.
3. Ijaz L, Mirza
B, Sheikh A. Inflammatory fibroid polyp causing recurrent colocolic
intussusception in a ten-year old boy: A case report. Babysurgeon.com [serial
online] 2009 [cited 2010 Dec 19]; 1. Available from: <http://www.babysurgeon.com/documents/cr-8-1-1.html>. (Archived by WebCite® at
http://www.webcitation.org/5lDdDi1X8)
<http://www.webcitation.org/5lDdDi1X8>
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Experience of intussusception in Fatima Memorial Hospital, Lahore- Incidence of
a lead point in intussusception. Pak J Pediatr Surg 1996;3:16-21.
5.
Mansoor H, Yousuf UF. Intussusception: What leads in children beyond infancy?
Ann King Edwards Med Uni 1998;4:31-2.
6. Burrington JD. Surgical
technique for the prevention of recurrent intussusception in childhood. Surg
Gynecol Obstet 1980;150:572-3.