Perineal Fistula With High Dilated Colon: One of a Special Type of Anorectal Malformations

Background The perineal stula with high dilated colon is a rare anomalous in the spectrum of anorectal malformations. The aim of this study is to explore the diagnosis and treatment of this special type of perineal stula (SPF), and to avoid the severe consequence due to misdiagnosis. Methods From March 2012 to January 2019, 7 patients who suffered from perineal stula with high dilated colon were retrospectively reviewed. Three were operated on primarily by our department, and 4 cases were re-operated after a perineal anoplasty repair performed elsewhere. Four were operated by laparoscopic anorectoplasty (LARP), and 3 cases were repaired by posterior sagittal anorectoplasty (PSARP). The follow-up outcomes were compared with 71 cases of normal perineal stula (NPF) in the same period. Results 7 cases have been followed up for 0.5-4 years (M=2.57±1.26) after denitive surgery. Their bowel function score (BFS) was lower than normal perineal stula (SPF=12, rang:5-18; NPF=18.5, rang:18-20). Four cases underwent anorectomanometry. The incidence of rectoanal inhibitory reex (RAIR) was lower in the special type group. (p=0.14). Three cases of barium enema angiography: 2 cases of colorectal dilatation and thickening changes, 1 case showed no obvious abnormalities. Conclusions Anorectal perineal stula should be examined by distal colostogram at preoperation. Select appropriate surgical approach is essential for children’s defecation function, and blind surgery can seriously affect long-term defecation function.

Conclusions Anorectal perineal stula should be examined by distal colostogram at preoperation. Select appropriate surgical approach is essential for children's defecation function, and blind surgery can seriously affect long-term defecation function.

Background
Perineal stula is one of the most common types of anorectal malformation in pediatric surgery. Most pediatric surgeons agree that this well recognized malformation can be repaired by perineal anoplasty. [1][2][3].
However, we experienced a rare case of a perineal stula associated with dilatation of the bowel found at a high position. This special type of malformation (SPF) is characterized by a perineal stula as the principal clinical manifestation but the stula tube is slender and the proximal bowel is found at a high position. Therefore, if a full preoperative assessment is not performed, the diagnosis may be delayed leading to abnormal bowel function. As Peña's paper in 2017 emphasized, a distal colostogram is the single most important diagnostic study indicated in children with an imperforate anus prior to de nitive repair [4]. The aim of this article is to explore the diagnosis and treatment of this special type of perineal stula, and to improve its treatment outcomes.

Methods
From March 2012 to January 2019, seven patients who had a anorectal malformation with a special type of perineal stula were either admitted or transferred to Department of Pediatric Surgery, Xinhua Hospital A liated to Shanghai Jiao Tong University School of Medicine. There are six boys and one girl. The time of diagnosis ranged from 2 days to 10 months after birth (mean [M] = 8.57 ± 107.70). The age at operation ranged from 2.7 to 12.6 months (M = 6.01 ± 2.88). The weight of the patients ranged from 6.2 to 11 kg (M = 7.46 ± 1.59). More than 50% of the SPF patients had a demonstrable cardiac defect (patent foramen ovale, PFO). Additionally, three patients had spine syndrome and two had some degree of urological anomaly (Table 1). Among these patients, four were diagnosed with low rectal perineal stula and had perineal anoplasty without undergoing a distal colostogram at a local hospital after birth. However, during the surgery, it was di cult to nd the blind end of the rectum, and therefore, the operation was terminated. After the perineal gland was sutured, a colostomy was performed. Thus, these patients only underwent colostomy before they were transferred to our institute after a period of three months. We performed a preoperative distal colostogram, which revealed that the stula tube was slender, and the dilated proximal colon was located in front of the iliac crest. (Fig. 1).
One patient was diagnosed with a rectal perineal stula at the local hospital, and was treated with daily anal sphincter treatment. When she was 10 months old, she developed anal bleeding after anal sphincter treatment, and was subsequently transferred to our hospital. On the basis of a preoperative distal colostogram and magnetic resonance imaging (MRI), the patient was diagnosed with SPF, and initially underwent transverse colostomy.
The two other patients who came to our hospital after birth were diagnosed with SPF by a preoperative distal colostogram similar to the above case. Subsequently, colostomy was performed in our hospital.
A standard statistical software package (Windows version 23.0; SPSS Inc., Armonk [NY], US) was used to analyze the data. Continuous variables are expressed as medians (ranges) and compared using Mann-Whitney U test. Use the chi-square test to compare categorical variables. P value less than or equal to 0.05 is considered statistically signi cant.

Results
All seven children underwent anal anorectoplasty at our hospital. Four patients underwent laparoscopic anorectoplasty (LAARP), and three cases were repaired using modi ed posterior sagittal anorectoplasty (PSARP). In all seven cases, the proximal dilatation of the bowel was found to be at a high position during the operation. Moreover, we found that the four children who underwent re-operation had serious scars at the original perineal surgery site and surrounding tissues. It was di cult to locate the external sphincter center point by electrical stimulation, and we nally completed the reconstruction surgery after combining with anatomical positioning (Table 2).
Clinical evaluation was carried out by using the seven-item bowel function score (BFS) by Rintala [5].
Refer to the previous scale study, the maximum total score is 20, the reference value of normal children is 19 with 18 being the 10th percentile [6,7]. Therefore, in this study, a value of 18 (over 90% of the control group) was used as the lower limit of normality. In addition, the manometric evaluation was performed simultaneously with the high-resolution anorectal manometry. The parameters measured in this study were the sphincter resting pressure, squeeze pressure, and the presence of rectal inhibitory re ex (RAIR).
The reference values for the normal sphincter resting pressure were 30 mmHg to 60 mmHg, and for the extrusion pressure were 50 mmHg to 120 mmHg. The follow-up outcomes were compared with 71 cases of normal perineal stula (NPF) in the same period.
Finally, anorectoplasty was performed successfully in all seven cases. All seven cases were followed up for 0.5-4.0 years (M = 2.57 ± 1.26) after the de nitive surgery. Six patients underwent regular outpatient follow-up, while one patient was followed up by telephone. During the follow-up, all seven patients had a seven-item bowel function score (BFS) and high-resolution anorectomanometry. Three cases also underwent barium enema angiography.
There was no signi cant difference in the BFS between the different surgical approaches. Three patients who underwent only one operation had no obvious symptoms such as incontinence and constipation. However, the four patients who underwent more than two repair operations demonstrated a lower BFS. Among them, one patient had constipation, while the remaining two exhibited fecal incontinence. Their BFS values were only 8, 10, 8, and 14, which are far below the normal range (Table 2).  Table 3).

Discussion
The de nition of perineal stula is undisputed and it is one of the most common anorectal malformations in pediatric surgery. However, the special type of perineal stula (SPF) with a highly dilated colon is very rare and the number of cases reported in the literature is limited to date. In our patients with SPF, the dilated proximal colon was located in front of the iliac crest, which undoubtedly contributed to the complexity of the operation.
In this study, incidence of the special type of perineal stula with high dilated colon was 8.97% (7/78). This incidence may re ect that surgeons often ignore to raise the importance of SPF. About 42.8% of all patients with SPF had spine syndrome of tethered cord which is far higher than NPF.
The diagnosis of perineal stula is well recognized, and almost all neonates can be diagnosed at birth. A true perineal stula is a narrow perineal foramen with no visible anal canal, and is located in the center of the anal sphincter but is not completely surrounded by the sphincter mechanism [9][10][11]. In boys, the stula is often found in the normal anal area and root of the scrotum. The stula in girls is mostly located between the normal anal area and posterior labia. The clinical presentation of SPF is similar to that of a perineal stula, but the position of the dilated colon is unlikely to be the same as in a normal perineal stula. However, some surgeons do not perform a preoperative examination to get a correct understanding of the anatomical structure of these anorectal malformations, including the related stula communication between the rectum and genitourinary tract. In our neonatal unit, all newborns with the anorectal malformation of a perineal stula were screened by a distal colostogram to con rm the position of the distal rectum. We found that there was a special type of perineal stula associated with a highly dilated colon. This special type of perineal stula, if unrecognized preoperatively, may complicate surgical operations to repair anorectal deformities. Therefore, it is imperative that a thorough evaluation (e.g., ddistal colostogram) be performed to identify an SPF so that it can be correctly treated. There is a lack of consensus in the literature on the best imaging method for accurate anatomical diagnosis at birth. Some authors believe that perineal ultrasound is the best option, while others prefer MRI [12,13]. We believe that no matter which investigation is used to assess the anatomy of the anorectal malformation, preoperative evaluation is essential in children diagnosed with a perineal stula to identify the possibility of a highly dilated colon. Therefore, we suggest a ddistal colostogram in the newborn period as well as a pelvic MRI to thoroughly evaluate the anatomy of the anorectal malformation.
Another important decision before surgery is to determine whether to transfer the patient to a center with extensive experience in pediatric surgery. Although there is no consensus on this point, there is strong evidence from adult studies that the surgeon's technique is independently associated with better outcomes [14][15][16]. In some local hospitals, surgeons may lack awareness of anorectal malformations. Therefore, we recommend that if there is no pediatric surgeon available at a local hospital, patients should be transferred to a center with extensive pediatric surgery experience.
In most patients born with a SPF, management includes a diverting colostomy. Colostomy is valuable because it can avoid the complications of secondary colon dilation and pseudo-incontinence [17]. In our case series, all patients were managed with a diverting colostomy before the de nitive repair.
Although it is the most straightforward anorectal malformation to repair [18,19], perineal stula remains a constant point of confusion. With regard to radical surgery, it is essential to select an appropriate surgical approach that ensures optimal defecation function, as blind surgery can seriously affect the long-term defecation function. In this study, we introduced the procedure of correcting this abnormality using a posterior sagittal approach and laparoscopic approach, which can accurately expose the position of the distal rectum. These two approaches can avoid potential complications of a stula, urethral injury, or intrasphincter anal dislocation.
Our routine is to calibrate the anus 3 weeks after surgery and continue to expand it for several months every day. With regard to the postoperative outcome of anorectal malformation treatment, particularly regarding continence, it has been reported that 100% of the patients have bowel control in recto-perineal stulas and the postoperative pain was also minimal [3]. In our study, 86% of the followed-up NPF patients were continent after the correction surgery at the end of the follow-up period. However, 57.1% of the SPF patients had abnormal bowel function, including constipation and fecal incontinence. Inadequate surgery, coupled with a natural propensity for constipation, can lead to severe fecal impaction that can cause substantial rectal dilation. This dilation can hamper rectal mobility and ultimately affect fecal control. In particular, when surgeons do not perform an adequate preoperative evaluation to accurately understand the anatomy of the anorectal malformation, including an associated stulous communication between the rectum and the urogenital tract, it may affect the optimal surgical management. Due to this, patients may have to undergo multiple operations and may develop a defecation dysfunction. In our study, children who underwent more than two repair operations had lower BFS than those who had only one operation. In addition, the BFS in SPF patients was lower than that in NPF patients, although the difference was not statistically signi cant. Therefore, repeated operations and a highly dilated colon may be risk factors for abnormal defecation function in these patients. Although the majority of these patients can be managed with drugs, careful follow-up is vital (as with all patients who have anorectal malformations), so that the patients who need early management of their bowel function can be identi ed [20].

Conclusions
In conclusion, this study reported a special type of perineal stula. Compared with NPF patients, the measurements of BFS and sphincter resting pressure on anorectal manometry were lower in SPF patients. To avoid a misdiagnosis, an anorectal perineal stula should be examined by a distal colostogram before repair. Selecting an appropriate surgical approach is essential for ensuring optimal defecation function in these children as blind surgery can seriously affect the long-term defecation function. The study was approved by the ethical committee of the Institutional Review Board of Shanghai Jiao Tong University. Informed written consent was obtained from the parents of each participant. Study procedure was carried out in accordance with the approved guidelines.

Consent for publication
Written informed consent for publication was obtained from all participants. All parents of the study participants gave written consent for their clinical details along with identifying images to be published in