|Year : 2022 | Volume
| Issue : 1 | Page : 71-76
Congenital pouch colon in girls: An algorithm for preoperative diagnosis
Amit Gupta, Amit Kumar, Rajiv Chadha, Partap Singh Yadav, Vikram Khanna, Subhasis Roy Choudhury
Department of Pediatric Surgery, Lady Hardinge Medical College, Kalawati Saran Children's Hospital, New Delhi, India
|Date of Submission||25-Sep-2020|
|Date of Acceptance||24-Jan-2021|
|Date of Web Publication||11-Jan-2022|
Dr. Amit Gupta
Department of Pediatric Surgery, Room No. 330, 3rd Floor, Kalawati Saran Children's Hospital, Bangla Sahib Road, New Delhi - 110 001
Source of Support: None, Conflict of Interest: None
| Abstract|| |
Aim: The aim of the study was o define the preoperative diagnostic clinical and radiological features in girls with congenital pouch colon (CPC).
Materials and Methods: Records of 47 girls with CPC, managed from 1996 to 2018, were reviewed. There were two age groups: Group A (newborn to 12 months; n = 26) and Group B (>12 months to 20 years; n = 21). The important clinical and radiologic features to help in a preoperative diagnosis were noted.
Results: The most common subtype was Type II (57.4%), followed by Type I (23.4%) and Type III (12.8%). The features common to both the groups were abdominal distension (A = 53.8%; B = 9.52%), severe perineal excoriation (A = 19.2%; B = 23/8%), and urinary incontinence (A = 30.7%; B = 85.7%). In addition, in Group B, fecaloma on abdominal palpation was noted in 28.6% of patients. The characteristic appearance of the perineum including external genitalia and findings on plain abdominal X-ray (AXR) were 100% accurate and hence diagnostic. These unique features helped us formulate an algorithm for preoperative diagnosis of this uncommon form of anorectal malformation in girls seen in North India.
Conclusions: The characteristic features on clinical examination should alert one to the presence of CPC in the outpatient clinic. The AXR was diagnostic in 100% of cases and is mandatory. If any doubt persists, examination of the genitalia under anesthesia with more retraction of the labial folds and endoscopy can be performed for confirmation. These measures should enable a clinician to make an accurate preoperative diagnosis in every girl with CPC.
Keywords: Anorectal malformation, congenital pouch colon, double vagina, urinary incontinence
|How to cite this article:|
Gupta A, Kumar A, Chadha R, Yadav PS, Khanna V, Choudhury SR. Congenital pouch colon in girls: An algorithm for preoperative diagnosis. J Indian Assoc Pediatr Surg 2022;27:71-6
|How to cite this URL:|
Gupta A, Kumar A, Chadha R, Yadav PS, Khanna V, Choudhury SR. Congenital pouch colon in girls: An algorithm for preoperative diagnosis. J Indian Assoc Pediatr Surg [serial online] 2022 [cited 2022 Jan 17];27:71-6. Available from: https://www.jiaps.com/text.asp?2022/27/1/71/335574
| Introduction|| |
Congenital pouch colon (CPC) is an unusual abnormality in which a pouch-like dilatation of a varying length of the shortened colon is associated with an anorectal malformation (ARM)., This condition has most frequently been reported from centers in northern India. CPC has been classified into four subtypes (Types I–IV) based on the length of normal colon proximal to the colonic pouch.
The anomalous anatomies in girls with CPC have described the colonic pouch fistula opening either into the vagina or in a persistent cloaca,,,,,,,,,, as a colovestibular fistula (colo-VF),,,,,,, a colovesical fistula,,,,,,, or even a colouterine fistula. A clearly discernible pattern in the abnormal anatomy was never described. However, two detailed studies reported from our center suggested that these girls did not have a “persistent cloaca” in the accepted sense of the term, as the external genitalia were essentially normal with a wide posterior margin of the vestibule and association with spinal or other major malformations was rare., All patients had double vagina with monocornuate uterus on each side of the pelvis and a high incidence of urinary incontinence (UI) (75%–81%) due to a widely open bladder neck, a small urinary bladder, and a short, wide urethra., The terminal fistula of the colonic pouch was closely apposed to the trigone and urethra and opened into the urethra or the vestibule in either a “high” or a “low” (more distal) intervaginal position., Similar findings have been described in a few other reports.,,,,,,,, Although there is a spectrum, the findings in our previous studies appeared to be constant and invariable., In addition, a preliminary abdominal X-ray (AXR) including the pelvis strongly indicates toward the presence of CPC.
The presence of a single perineal opening on preliminary examination on light labial retraction in those with a “high” confluence of the urethral and vaginal openings can however still lead to a misdiagnosis of persistent cloaca. Girls with CPC and a colo-VF can also mistakenly be diagnosed as having ARM with rectovestibular fistula (recto-VF). Another important feature is that a large number of girls with CPC may present beyond infancy if evacuation is fairly effective through the fistula.,,,,
As the management protocol of CPC is vastly different, it is essential to diagnose the anomaly preoperatively. The aim of the present study is to define the important predictive findings and formulate an algorithm to diagnose this anomaly with high accuracy preoperatively.
| Materials and Methods|| |
In this retrospective study, the records of 47 girls with CPC managed at our center over a 22-year period (1996–2018) were reviewed. The patients were divided into two groups according to the age at presentation or availability of records: Group A (newborn to 12 months; n = 26) and Group B (>12 months to 20 years; n = 21). The subtypes of CPC were Type I (n = 11; 23.4%), Type II (n = 27; 57.44%), and Type III CPC (n = 6; 12.76%). In three patients, the subtype of CPC had not been recorded as they left the hospital before surgery, but the clinical and radiologic features were diagnostic of CPC. Examination in the outpatient department (OPD) supplemented by an examination under anesthesia (EUA) allowed for comprehensive evaluation. We analyzed the occurrence of various features which appeared vital for diagnosis and formulated an algorithm for accurate diagnosis preoperatively.
| Results|| |
In Group A patients (n = 26) [Table 1], important clinical findings were abdominal distension, often marked (n = 14; 53.8%), frequent passage of small amounts of stools and gas from the perineal opening, partial or complete UI (n = 6; 23%), a suspicion of UI (n = 2; 7.7%), and severe perineal excoriations (n = 5; 19.2%). Three “characteristic” features were noted on preliminary examination of the external genitalia and perineum in OPD: (1) a wide posterior margin of the vestibule in all (100%) [Figure 1], in combination with either of these two, (2) separate openings of the urethra and double (often “tilted”) vagina with a wide intervaginal bridge; usually showing vaginal mucosa clearly on gentle retraction of the labial folds [Figure 2]a; this was seen in OPD in only 9 (34.6%) patients, or (3) the urethra and double vagina were confluent cranially in 17 patients (65.4%) through a “single opening” seen on gentle retraction in OPD examination, with folds radiating inward from the margins of the vulval vestibule to the point of confluence also described as the “clover leaf” appearance [Figure 2]b; this confluence could be appreciated very well with greater retraction of the labial folds possible on EUA, without any need for genitoscopy. The urethral and vaginal confluence was at a more cranial level in 12 patients (46.2%) [Figure 2], while an intermediate picture was present in the remaining 5 girls (19.2%). The colonic pouch ended in a “low” colo-VF (n = 5) [Figure 3], an anterior perineal fistula just posterior to the double vaginas (n = 1), while in 20 patients, the opening of the fistula could not be identified. A fourth peculiar feature noted in 4/7 (57.1%) where photographs were available in records was stretched-out perineum receding inward just posterior to the vestibule [Figure 2]a. AXR was available in 21 patients (81%); it showed either of the two findings in all cases (100%) – a large gas shadow or an air–fluid level (AFL) in the left side of the abdomen (n = 16; 76.2%) [Figure 4]a or a large gas shadow with inspissated fecal matter on the left side abdomen (n = 5; 23.8%). In one patient, in addition to the large AFL, pneumoperitoneum due to perforation of the colonic pouch was also present. Sacrum was normal in 20/21 (95.2%) patients [Figure 4]a and partial sacral agenesis was seen in one patient.
|Table 1: Summary of our findings in Group A (newborn to 12 months) and Group B: >12 months to 20 years|
Click here to view
|Figure 1: Normal appearance of external genitalia with “wide posterior margin of vestibule”|
Click here to view
|Figure 2: (a) “Low” confluence of openings of the urethra and the two vaginas (fine arrows) in a 3-month old girl with Type II congenital pouch colon. Note the recession in area of perineum posterior to vestibule (broad arrow). (b) External genitalia in a 2-day-old girl with Type I congenital pouch colon showing “clover-leaf” appearance of folds radiating inward and cranially from the margins of the wide vestibule (arrows) suggesting high confluence of urethral and vaginal openings|
Click here to view
|Figure 3: External genitalia in a 6-month-old girl with Type III congenital pouch colon and a “low” colovestibular fistula (catheter). Note the two vaginas (V) with wide intervaginal bridge|
Click here to view
|Figure 4: (a) Abdominal X-ray in a newborn girl with Type II congenital pouch colon showing a large left-sided abdominal gas shadow. Note the normal sacrum. (b) Abdominal X-ray in a 2-year-old girl with Type I congenital pouch colon showing a large radio-opacity on the left side of a distended abdomen due to inspissated, accumulated fecal matter (arrow)|
Click here to view
In Group B patients (n = 21) [Table 1], at presentation, abdominal distension was present in two patients (9.5%); and extensive peri-vulval excoriations were noted in five patients (23.8%) [Figure 5]a. In six patients (28.6%), the abdomen had a doughy feel on palpation, perhaps due to the fecaloma in the distended colonic pouch. UI was present in 18 patients (85.7%); of these, partial UI in 5 (23.8%) and complete UI in 13 patients (61.9%) were seen. Examination showed characteristic features of the external genitalia described above in Group A in all 21 patients (100%). OPD examination showed only a single, though wide, perineal opening in 8 of these 21 patients (38.1%) [Figure 5]a; the confluent urethral and vaginal orifices could be appreciated well with greater retraction of the labia on EUA without any need for genitoscopy [Figure 5]b. In older patients, a wide intervaginal bridge was more apparent between the two vaginal openings [Figure 6]a and [Figure 6]b. The fistulous opening of the colonic pouch could be seen in ten patients (47.6%); it was closely apposed to the trigone and urethra and opened posterior to the urethral opening in seven patients – “low” (intervaginal) vestibular fistula (VF) in five [Figure 6]a and “high” or more cranially placed VF in two. The fistula opened into the distal urethra just within the wide urethral meatus in three patients [Figure 6]b and into the proximal urethra in another three patients on cystourethrogenitoscopy. The opening of the fistula was not identified in the records of 8 patients (38.1%). In addition, stretched-out perineum receding inward just posterior to the vestibule was noted in 6/11 patients (55.55%) in the available photographic records [Figure 5]b. AXR was available in 18 patients; all showed either a gas shadow or AFL mostly in young patients or a large radio-opacity on the left side of a distended abdomen due to fecaloma, especially in older girls and a normal sacrum [Figure 4]b. With these features, a preoperative diagnosis of CPC had been made in 17/24 (70.83%) girls with CPC in the last 10-year period from 2009 to 2018. An algorithm to maximize chances of preoperative diagnosis is shown in [Table 2].
|Table 2: Algorithm for preoperative diagnosis of congenital pouch colon in girls|
Click here to view
|Figure 5: (a) A 15-month–old girl with Type II congenital pouch colon showing a single perineal opening. (b) On retraction of labial fold, the openings of the urethra and vaginas. Arrow points to inwardly receded perineum|
Click here to view
|Figure 6: (a) External genitalia in a 10-year-old girl with Type II congenital pouch colon and distal colo-urethral fistula (arrow). Note wide urethral meatus, wide inter-vaginal bridge, and extensive “peri-vulval excoriations.”Reproduced with permission from [Figure 7] in Chadha and Khan. (b) External genitalia in a 12-year-old girl with Type II congenital pouch colon and a “low” colo-vestibular fistula. Note the wide intervaginal bridge|
Click here to view
| Discussion|| |
Although clinical features like marked abdominal distension in newborns and infants and poorly managed constipation with overflow incontinence in older girls are important findings suggesting the possibility of CPC in girls with ARM, the characteristic features on examination of the external genitalia are quite unique., A history of UI is an additional feature pointing to the diagnosis. Often, in the newborn or infant in diapers, the presence of UI may be missed initially, especially as UI may be partial and the child would also be passing urine intermittently in a stream. However, as in 2 infants (7.7%) from the present study, careful questioning may elicit that the parents have noticed leakage of urine when the child strains or sometimes even in the standing posture. UI is more clearly apparent in older girls, and in the present study, a history suggestive of UI was present in 18/21 (85.7%) older girls and only in 8/26 (30.6%) newborns or infants. Apart from the characteristic features of the external genitalia, peri-vulval excoriations due to UI may also be present., In older girls, the underlying inspissated fecal matter in the large colonic pouch gave a doughy feel to the abdomen on palpation.
As shown by the algorithm for diagnosis [Table 2], AXR findings are usually conclusive, even in older girls in whom a large radio-opacity on the left side of a distended abdomen due to inspissated accumulated fecal matter in the colonic pouch is often a very characteristic finding. As described earlier, at least in reports from the Indian subcontinent, despite behaving as a high type of ARM, CPC is infrequently associated with sacral anomalies or major malformations involving other organ systems., In the present study, a normal sacrum was present in 38/39 patients (97.4%) and this finding is also an important pointer toward the diagnosis.
A colo-VF is often present in girls with CPC and may be visible on initial examination or at EUA as in 19/47 (40.4%) patients in this series. In cases of CPC with a low confluence of the perineal openings, an erroneous diagnosis of ARM with recto-VF is therefore very much possible, especially as recto-VF is also associated with a septate vagina in as many as 6% cases. In addition to the important differentiating features described earlier, in 55.55% (Group A = 4/7, Group B = 6/11) girls in our series, the whole perineum appeared receded inward, and the area of the anal dimple appeared wide and stretched out. Similar findings reported earlier, is an additional diagnostic feature.
The differentiation of CPC from persistent cloaca is also important as the management protocol for both conditions is vastly different. The external genitalia are hypoplastic in cloaca, contrary to grossly normal appearance with wide posterior margin of vestibule in CPC. Cloacal anomalies are often associated with major GU anomalies including hydrocolpos, sacral anomalies, and major malformations involving other major organ systems;, these are characteristically absent in CPC. In addition to the preliminary colostomy for the ARM, associated urologic anomalies in cloaca require detailed assessment and may need emergent management.
The importance of distinguishing CPC with a colo-VF from recto-VF cannot be overemphasized. Recto-VF is usually managed by a single-stage procedure, limited PSARP, in infancy, although a preliminary colostomy is recommended for certain specific indications. If the presence of CPC is undiagnosed preoperatively, the procedure performed would be fraught with complication as the colo-VF tract is closely apposed to the urethra and trigone in an intervaginal position, and the consequences of damaging these structures and/or the two vaginas may be serious. In addition, management of the colonic pouch is in itself an additional necessity. Agarwal et al. reported a case of CPC with a VF misdiagnosed as a recto-VF in whom initial limited PSARP for the VF was followed by wound disruption. Type I CPC was detected only during a diverting colostomy and the child ultimately required a three-stage reconstruction for the anomaly.
It has been suggested that in girls with a VF who do not decompress well despite a wide fistula orifice, a barium enema should routinely be performed to rule out CPC., In our view, a contrast enema through a VF, if present, should rarely be required as the diagnostic protocol described here [Table 2] should enable preoperative diagnosis of CPC. Perhaps, the only indication should be the rare older girl with a colo-VF in whom the typical features of the external genitalia, perineum, anal dimple, and AXR findings are inconclusive.
Declaration of patient consent
The authors certify that they have obtained all appropriate patient consent forms. In the form the patient (s) has/have given his/her/their consent for his/her/their images and other clinical information to be reported in the journal. The patients understand that their names and initial s will not be published and due efforts will be made to conceal their identity, but anonymity cannot be guaranteed.
Financial support and sponsorship
Conflicts of interest
There are no conflicts of interest.
| References|| |
Narasimharao KL, Yadav K, Mitra SK, Pathak IC. Congenital short colon with imperforate anus (pouch colon syndrome). Ann Pediatr Surg 1984;1:159-67.
Chadha R, Bagga D, Malhotra CJ, Mohta A, Dhar A, Kumar A. The embryology and management of congenital pouch colon associated with anorectal agenesis. J Pediatr Surg 1994;29:439-46.
Rao KL, Menon P. Congenital pouch colon associated with anorectal agenesis (pouch colon syndrome). Pediatr Surg Int 2005;21:125-6.
Singh A, Singh R, Singh A. Short colon malformation with imperforate anus. Acta Paediatr Scand 1977;66:589-94.
Trusler GA, Mestel AL, Stephens CA. Colon malformation with imperforate anus. Surgery 1959;45:328-34.
Sarin YK, Nagdeve NG, Sengar M. Congenital pouch colon in female subjects. J Indian Assoc Pediatr Surg 2007;12:17-21. [Full text]
Wakhlu AK, Tandon RK, Kalra R. Short colon with anorectal malformation. Indian J Surg 1982;44:621-9.
Wakhlu AK, Wakhlu A, Pandey A, Agarwal R, Tandon RK, Kureel SN. Congenital short colon. World J Surg 1996;20:107-14.
Mathur P, Saxena AK, Simlot A. Management of congenital pouch colon based on the Saxena-Mathur classification. J Pediatr Surg 2009;44:962-6.
Ghritlaharey RK, Budhwani KS, Shrivastava DK, Gupta G, Kushwaha AS, Chanchalani R, et al
. Experience with 40 cases of congenital pouch colon. J Indian Assoc Pediatr Surg 2007;12:13-6. [Full text]
Chadha R, Gupta S, Mahajan JK, Bagga D, Kumar A. Congenital pouch colon in females. Pediatr Surg Int 1999;15:336-42.
Patil RT, Gupta RK, Sanghvi B. Unusual variants of cloaca- six cases. J Indian Assoc Pediatr Surg 2009;14:156.
Wester T, Läckgren G, Christofferson R, Rintala RJ. The congenital pouch colon can be used for vaginal reconstruction by longitudinal splitting. J Pediatr Surg 2006;41:e25-8.
Boleken ME, Yildiz E, Kaya M, Deniz M. Appendix duplication in association with persistent cloaca and type 2 pouch colon. Int J Anat Var 2010;3:12-4.
Chadha R, Choudhury SR, Pant N, Jain V, Puri A, Acharya H, et al
. The anomalous clinical anatomy of congenital pouch colon in girls. J Pediatr Surg 2011;46:1593-602.
Chadha R, Khan NA, Shah S, Pant N, Gupta A, Choudhury SR, et al
. Congenital pouch colon in girls: Genitourinary abnormalities and their management. J Indian Assoc Pediatr Surg 2015;20:105-15.
] [Full text]
Demirogullari B, Ozen IO, Afsarlar C, Moralioglu S, Poyraz A, Sonmez K, et al
. Congenital pouch colon associated with anorectal malformation: Report of 2 cases. J Pediatr Surg 2007;42:E13-6.
Gharpure V. Is progressive pneumoperitoneum useful in delayed repair of large omphaloceles? J Indian Assoc Pediatr Surg 2008;13:109-10.
] [Full text]
Kurt G, Celayir AC, Sarica K. The Importance of Stoma Leveling of Pouch Colon in Cases with Persistent Cloaca. Paper Presented at the 25th
Annual Congress of the EPSA (Egyptian Pediatric Surgical Association) & TAPS (Turkish Association of Pediatric Surgeons) & SECI (South Egypt Cancer Institute), Luxor, Egypt, 2009. (OP 47).
Uotani C, Ishimaru T, Konishi K, Fujishiro J, Sugiyama M, Komuro H, et al
. A case of a girl with congenital pouch colon. Jpn J Pediatr Surg 2014;50:808-13. [doi: 10.11164/jjps. 50.4_808].
De La Torre-Mondragón L, Santos-Jasso KA, Palestina-Carro O, Ruiz-Montañez A. Colonic pouch syndrome (colon pouch) in the spectrum of anorectal malformations. Acta Pediatr Mex 2013;34:132-40.
Levitt MA, Bischoff A, Breech L, Peña A. Rectovestibular fistula – Rarely recognized associated gynecologic anomalies. J Pediatr Surg 2009;44:1261-7.
Mirza B, Ahmad S, Sheikh A. Congenital pouch colon: A preliminary report from pakistan. J Neonatal Surg 2012;1:37.
Chadha R, Khan NA. Congenital pouch colon. J Indian Assoc Pediatr Surg 2017;22:69-78.
] [Full text]
Patel JN, Kumar A, Yadav PS, Chadha R, Datta V, Roy Choudhury S. The position of the anal dimple in newborns and infants with anorectal malformations and its correlation with the normal anal position. J Pediatr Surg 2018;53:1560-5.
Tanwani R, Maheshwari M, Maheshwari M. Study of congenital pouch colon anomaly in Ahmedabad region. IJDR 2015;5:4455-60.
Levitt MA, Peña A. Anorectal malformations. In: Coran AG, Adzick NS, Krummel TM, Laberge JM, Shamberger RC, Caldamone AA, editors. Pediatric Surgery. 7th
ed. Philadelphia, PA: Elsevier, Saunders; 2012. p. 1289-310.
Agarwal G, Bhagwat A, Bhusare D. Pitfall in the one-stage management of rectovestibular fistula: A rare variant of congenital pouch colon. MGM J Med Sci 2016;3:154-5.
Menon P, Rao KL. Primary anorectoplasty in females with common anorectal malformations without colostomy. J Pediatr Surg 2007;42:1103-6.
[Figure 1], [Figure 2], [Figure 3], [Figure 4], [Figure 5], [Figure 6]
[Table 1], [Table 2]