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A. W a k h l u • A. P a n d e y • A. P r a s a d • S. N. K u r e e l
R. K. T a n d o n • A. K. W a k h l u
Perineal canal
Abstract Perineal canal (PC) is a rare anomaly constitut- which there is a fistula between the anterior wall of a
ing 4% of all anorectal malformations. Sixty patients (56 normally-formed anus/rectum and the vestibule/perineum
females and 4 males) with PC managed over the past in females or the perineum/anterior urethra in males. Since
27 years are reported. The ages ranged from 2 days to the initial reports by Bryndorf and Madsen [1] and Pegum
13 years. The chief symptom was passage of fecal matter et al. [7], patients with PC have been reported mostly from
through both the anus and the fistula. One girl had under- Asian countries [3]. Although the diagnosis is straightfor-
gone previous, unsuccessful surgery. All our patients were ward, the conventional treatment of this anomaly leaves
treated by anterior sagittal anorectoplasty (ASARP), which much to be desired. The present paper details our experi-
allowed anatomic exposure and accurate repair of the ence with the management of PC over the past 25 years. We
anomaly. In 49 patients without any perineal inflammation also describe a surgical technique that has given consis-
primary A S A R P was undertaken. Surgery was delayed in tently good results.
11 patients with perineal excoriations and/or active inflam-
mation. One patient died post-operatively due to unrelated
causes and 1 developed a recurrence. Anal dilation was
Materials and methods
required in 7 cases. Fifty patients were seen at first follow-
up 12 weeks after surgery. All were continent and had
Of 1600 patients with ARM treated at our hospital between 1969 and
normal defecation without the use of laxatives. Thirty-four 1995, there were 60 with PC (3.8%), who constituted 7.3% (56/776) of
could be followed up to the age of 3 years; they were females with ARM (Table 1).
continent with normal bowel habits. There was no shift in In female patients the chief symptom was defecation through both
the position of the anus and no instance of rectal dilation. the anus and the fistula (Table 2). The parents of one 6-year-old girl
attributed the malformation to a sexual assault. In another girl with
Individualization of the management and operation by the
anterior sagittal approach thus offers good results in this
uncommon anorectal anomaly. Table 1 Age and sex distribution of the patients