Abstract
Purpose: No single surgical procedure for total colonic aganglionosis has clearly been proven
to be superior. We present our experience and the long-term results of a standard
Duhamel's pull-through procedure in the management of this rare form of Hirschsprung's
disease. Material and Methods: A retrospective study of all cases with Hirschsprung's disease diagnosed in our institute
from November 1983 to December 2004 was conducted. All operated patients with total
colonic aganglionosis (TCA) had a diversion in the first week of life. Duhamel's pull-through
was the definitive procedure for all operated patients and was performed between 6
months and 1 year of age. All patients and their parents were contacted for an extended
follow-up, ranging between 30 months and 21 years. Incontinence was assessed on the
basis of soiling in the diaper between two consecutive defecations in the younger
group of patients and the need for a diaper in the older age group. Hirschsprung's
enteritis was regarded as severe if the patient's condition did not improve on conservative
management and the patient needed an ileostomy post-pull-through. Results: Thirty-six cases with Hirschsprung's disease were diagnosed during the study period.
Twelve patients (31.4 %) had total colonic aganglionosis, confirmed at laparotomy,
and underwent a diversion. Eight underwent definitive surgery during the first year
of life. All operated patients had a standard Duhamel's pull-through as the definitive
procedure. Four cases were not operated: two had Waardenburg syndrome with lethal
total aganglionosis, one had multiple anomalies, and the last patient with mid-jejunal
involvement died while awaiting a definitive procedure. Familial incidence was apparent
in two sets of siblings. Leakage followed by stricture occurred in one patient. Hirschsprung's
enteritis was diagnosed in three patients. In two, the enteritis was mild, while one
patient required an ileostomy which was performed elsewhere. Half of our patients
have an almost normal number of daily bowel movements (1 – 2 times). Conclusions: The long-term results of a standard Duhamel's pull-through for TCA are good in terms
of continence, bowel motion, and physical development.
Key words
TCA - aganglionosis - Duhamel's procedure - pull‐through
References
- 1
Applebaum H, Richardson R J, Wilkinson G A, Warden M J.
Alternative operative procedure for total colonic aganglionosis.
J Pediatr Surg.
1988;
23
49-51
- 2
Emslie J, Krishnamoorthy M, Applebaum H.
Long-term follow-up of patients treated with ileoendorectal pull-through and right
colon onlay patch for total colonic aganglionosis.
J Pediatr Surg.
1997;
32
1542-1544
- 3
Endo M, Masuyama H, Watanabe K, Ikawa H, Yokoyama J, Kitajima M.
Motor activity of refashioned colo-recto-anus in patients with total colonic aganglionosis.
J Pediatr Surg.
1996;
31
283-290
- 4
Endo M, Watanabe K, Fuchimoto Y, Ikawa H, Yokoyama J.
Long-term results of surgical treatment in infants with total colonic aganglionosis.
J Pediatr Surg.
1994;
29
1310-1314
- 5
Fouquet V, De Lagausie P, Faure C, Bloch J, Malbezin S, Ferkhadji L, Bauman C, Aigrain Y.
Do prognostic factors exist for total colonic aganglionosis with ileal involvement?.
J Pediatr Surg.
2002;
37
71-75
- 6
Hoehner J C, Ein S H, Shandling B, Kim P C.
Long-term morbidity in total colonic aganglionosis.
J Pediatr Surg.
1998;
33
961-965
965-966
- 7
Ikawa H, Masuyama H, Hirabayashi T, Endo M, Yokoyama J.
More than 10 years' follow-up to total colonic aganglionosis – severe iron deficiency
anemia and growth retardation.
J Pediatr Surg.
1997;
32
25-27
- 8
Ikeda K, Goto S.
Total colonic aganglionosis with or without small bowel involvement: an analysis of
137 patients.
J Pediatr Surg.
1986;
21
319-322
- 9
Inoue K, Shimotake T, Iwai N.
Mutational analysis of RET/GDNF/NTN genes in children with total colonic aganglionosis
with small bowel involvement.
Am J Med Genet.
2000;
93
278-284
- 10
Ludman L, Spitz L, Tsuji H, Pierro A.
Hirschsprung's disease: functional and psychological follow up comparing total colonic
and rectosigmoid aganglionosis.
Arch Dis Child.
2002;
86
348-351
- 11
Nichol P F, Harms B A, Go L L, Lund D P.
Ileo-anal S-pouch reconstruction in patients with total colonic aganglionosis after
failed pull-through procedure.
J Pediatr Surg.
2004;
39
e7-e9
- 12
Ross M N, Chang J H, Burrington J D, Janik J S, Wayne E R, Clevenger P.
Complications of the Martin procedure for total colonic aganglionosis.
J Pediatr Surg.
1988;
23
725-727
- 13
Solari V, Piotrowska A P, Puri P.
Histopathological differences between recto-sigmoid Hirschsprung's disease and total
colonic aganglionosis.
Pediatr Surg Int.
2003;
19
349-354
- 14
Suita S, Taguchi T, Kamimura T, Yanai K.
Total colonic aganglionosis with or without small bowel involvement: a changing profile.
J Pediatr Surg.
1997;
32
1537-1541
- 15
Tomiyama H, Shimotake T, Ono S, Kimura O, Tokiwa K, Iwai N.
Relationship between the type of RET/GDNF/NTN or SOX10 gene mutations and long-term
results after surgery for total colonic aganglionosis with small bowel involvement.
J Pediatr Surg.
2001;
36
1685-1688
- 16
Tsuji H, Spitz L, Kiely E M, Drake D P, Pierro A.
Management and long-term follow-up of infants with total colonic aganglionosis.
J Pediatr Surg.
1999;
34
158-161
162
Dr. Enaam H. Raboei
Department of Pediatric Surgery
King Fahd Armed Forces Hospital
P. O. Box 9862
21159 Jeddah
Saudi Arabia
Email: enaamraboei@yahoo.fr