scholarly journals Varied Presentation of Congenital Segmental Dilatation of the Intestine in Neonates: Report of Three Cases

2016 ◽  
Vol 5 (4) ◽  
pp. 55 ◽  
Author(s):  
Binod Kumar Rai ◽  
Bilal Mirza ◽  
Imran Hashim ◽  
Muhammad Saleem

Congenital segmental dilatation (CSD) of the intestine is a rare developmental anomaly characterized by sharply demarcated dilatation of a gastrointestinal segment and may present with intestinal obstruction. We report three cases of CSD of the intestine in neonates with varied presentation. First patient was mistaken as pneumoperitoneum on abdominal radiograph, which led to initial abdominal drain placement. The 2nd patient was a case of anorectal malformation associated with congenital pouch colon (CPC) and CSD of ileum; and the third case presented as neonatal intestinal obstruction and found to have CSD of ileum. All the patients were successfully managed in our department.

2015 ◽  
Vol 4 (1) ◽  
Author(s):  
Bilal Mirza ◽  
Muhammad Saleem

Postoperative neonatal intestinal obstruction has a myriad of etiology. An operated case of imperforate anus developed intestinal obstruction early postoperatively. At re-operation, missed complete congenital pouch colon with a small perforation and displacement of small bowel into the lesser sac were found. The patient was managed by adhesionolysis, excision of pouch colon, and end ileostomy. The patient did well postoperatively.


2017 ◽  
Vol 6 (2) ◽  
pp. 38 ◽  
Author(s):  
Prince Raj ◽  
Hirendra Birua

Congenital pouch colon (CPC) or short colon syndrome is a rare type of anorectal malformation(ARM). Type V is the rarest form of CPC. We present a 1-day-old male child with type V CPC with prune belly syndrome and congenital anterior urethrocutaneous fistula (CAUF).


2018 ◽  
Vol 15 (1) ◽  
pp. 10
Author(s):  
Rossella Angotti ◽  
QadirQadir Mohamed Salih ◽  
Francesco Molinaro ◽  
Francesco Ferrara ◽  
Marina Sica ◽  
...  

2021 ◽  
Vol 10 ◽  
pp. 33
Author(s):  
Praveen Mathur ◽  
Sharanabasappa Gubbi ◽  
Aadil Farooq ◽  
Priyanka Mittal ◽  
Gunjan Sharma

Background: Congenital pouch colon (CPC) is a rare variant of high anorectal malformation. More and more varied associations of CPC with other entities are being added to the literature. Case presentation: A 1-day-old male baby presented to the emergency room with marked abdominal distension and absent anal opening. On exploration, the baby was found to have CPC (Type 2) with colonic atresia. This association has not been reported in English literature. Conclusion: This is a report of a case of type 2 CPC with colonic atresia. To the best of our knowledge, such an association has not been reported so far. The final embryological outcome is dictated both by the topography and timing of vascular insult.


2015 ◽  
Vol 57 (3) ◽  
pp. 193-197 ◽  
Author(s):  
Salah S. Mahmood ◽  
◽  
Ahmed Z. Zain ◽  
Raghad J. Aboalhab ◽  
◽  
...  

2021 ◽  
Vol 11 (2(40)) ◽  
pp. 33-40
Author(s):  
O.D. Fofanov ◽  
V.O. Fofanov ◽  
А.P. Yurtseva

The article presents literature data andown observations of some rare congenital malformationsof the colorectal area in newborns that require surgicaltreatment. These are defects such as congenital pouch colonand congenital segmental dilatation of the colon. Thereare isolated cases of birth of children with these defectsin European countries and North America. They are morecommon in Asian countries, especially in India. Diagnosisand surgical correction of such congenital malformationscause difficulties associated with insufficient awarenessof pediatric surgeons, neonatologists, pediatricians aboutthis pathology. Data is presented on clinical manifestations,antenatal and postnatal diagnosis and treatment tactics, aswell as the histopathological structure of the affected colonin these defects.The analysis of literature data and the presented clinicalobservations of congenital pouch colon and congenitalsegmental dilatation of the colon in newborns indicate thepossibility of their antenatal and preoperative diagnosis.It is concluded that children with anorectal malformationsand Hirschsprung's disease require a thorough differentialdiagnosis with congenital pouch colon and segmentaldilatation of the colon, as the tactics of their surgicalcorrection significantly differ from the treatment tacticsof common anorectal malformations and Hirschsprung'sdisease surgical management.


2020 ◽  
Vol 24 (1) ◽  
pp. 26-31
Author(s):  
AK Mostaque ◽  
Sayed Zahid Hossain

Background: Neonatal surgery (NS) is an extremely challenging leading edge of pediatric surgery. In our country NS death were 8% due to treatable congenital anomalies. The objectives of study were to observe yearly admission of NS patients, age of presentation, anthropometric records, prenatal record and types of congenital anomalies, and mortality of treated neonates. Materials and Methods: This cross-sectional study was conducted on 337 admitted neonates to assess the state of 70 consecutive NS patients admitted in the Pediatric Surgery ward. Birth weight was compared with randomly selected and sex matched 154 were neonatology neonates (NN), and 113 delivered un-admitted healthy neonates of the labor-ward (LN). The variables observed were number of neonatal surgical patients admitted, age of presentation, birth and admission weight, prenatal ultrasonogram for fetal anomalies and the types of anomalies, outcome (mortality) of neonatal surgery. Results: The mean age of surgical neonates at the time of admission was 5.7 ± 6.39 (1-25) days. Mean birth weight of surgical and neonatology neonates was 2.66 ± 0.76 (1.5-4.5) kg and 2.24 ± 0.71 (0.9-4) kg respectively. The difference was significant (p < 0.01). The mean admission weight of the surgical and neonatology neonates were 2.57 ± 0.66 (1.4-4.1) kg and 2.25 ± 0.62 (0.8-4.1) kg respectively showing significant difference (p < 0.01). Ten percent of NS patients and 38.3% of NN patients had records of prenatal ultrasonogram, and their reports were normal fetus. The difference was significant (Z = 4.36). Eighty seven percent NS patients and 49% NNs were delivered at home and the difference was significant (Z = 4.49). Major surgical problem were anorectal malformation (48.6%) and neonatal intestinal obstruction (20%). The treatments given to the patient admitted in the pediatric surgery ward were emergency laparotomy with resection-anastomosis, ileostomy, and transverse loop colostomy in 29 (41.3%), anoplasty 21 (30%), incision and drainage of abscess 5 (7.1%), and conservative treatment 15 (21.43%). The mortality rate of neonatal surgical and neonatology patients was 12.9% and 13% respectively. Conclusion: The number of NS patients (work load) indicated the necessity of establishment of a NS unit which could be viable. The mortality of NS patients were due to low birth weight, and delivery at home causing transport delay from birth place to the pediatric surgery ward because of lack of prenatal awareness of presence of congenital anomalies. Anorectal malformation is the commonest congenital anomaly, followed by neonatal intestinal obstruction. Emergency laparotomy was the major surgical intervention offered. To improve the survival of the NS patients, prenatal diagnosis of the congenital anomaly, mandatory delivery at defined hospital, rapid transport of the surgical neonates born away from hospital, and establishment of a NS unit in tertiary level hospitals were indicated. Journal of Surgical Sciences (2020) Vol. 24 (1) : 26-31


2011 ◽  
Vol 16 (2) ◽  
pp. 61 ◽  
Author(s):  
Rajiv Chadha ◽  
Archana Puri ◽  
SubhashisRoy Choudhury ◽  
PartapSingh Yadav ◽  
JitendraKumar Kumar ◽  
...  

Sign in / Sign up

Export Citation Format

Share Document