scholarly journals Type V congenital pouch colon: An extremely rare variant of anorectal malformations

2017 ◽  
Vol 22 (2) ◽  
pp. 122 ◽  
Author(s):  
Sudhir Singh ◽  
JD Rawat ◽  
Nitin Pant ◽  
Digamber Chaubey
Keyword(s):  
Rare Variant ◽  
Anorectal Malformations ◽  
Congenital Pouch Colon ◽  
Pouch Colon ◽  
Type V

scholarly journals Type V Pouch Colon, Prune Belly Syndrome, and Congenital Anterior Urethrocutaneous Fistula

2017 ◽  
Vol 6 (2) ◽  
pp. 38 ◽  
Author(s):  
Prince Raj ◽  
Hirendra Birua
Keyword(s):  
Anorectal Malformation ◽  
Male Child ◽  
Prune Belly Syndrome ◽  
Urethrocutaneous Fistula ◽  
Rare Type ◽  
Prune Belly ◽  
Short Colon ◽  
Congenital Pouch Colon ◽  
Pouch Colon ◽  
Type V

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).

scholarly journals Type V congenital pouch colon: A need to expand the scope of the definition

2015 ◽  
Vol 20 (2) ◽  
pp. 101
Author(s):  
Rajiv Chadha ◽  
ShindeNand Kishore ◽  
SubhasisRoy Choudhury
Keyword(s):  
Congenital Pouch Colon ◽  
Pouch Colon ◽  
Type V

scholarly journals RARE COLORECTAL MALFORMATIONS IN NEWBORNS. LITERATURE REVIEW AND OWN OBSERVATIONS

2021 ◽  
Vol 11 (2(40)) ◽  
pp. 33-40
Author(s):  
O.D. Fofanov ◽  
V.O. Fofanov ◽  
А.P. Yurtseva
Keyword(s):  
North America ◽  
Literature Review ◽  
Clinical Manifestations ◽  
Anorectal Malformations ◽  
Asian Countries ◽  
Postnatal Diagnosis ◽  
Segmental Dilatation ◽  
Congenital Pouch Colon ◽  
Pouch Colon ◽  
Pathology Data

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.

scholarly journals Congenital Pouch Colon without Fistula: A Rare Variant

2020 ◽  
Vol 8 (4) ◽  
pp. 38
Author(s):  
Vinita Chaturvedi ◽  
Rahul Gupta ◽  
Neeraj Tuteja ◽  
Dinesh Kumar Barolia ◽  
Ravitej Bal
Keyword(s):  
Rare Variant ◽  
Congenital Pouch Colon ◽  
Pouch Colon

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scholarly journals A Terminal Colovesical Fistula in an Anorectal Malformation

2020 ◽  
Vol 7 ◽  
pp. 2333794X2095332
Author(s):  
Jayalaxmi Shripati Aihole
Keyword(s):  
Anal Canal ◽  
Anorectal Malformation ◽  
Rare Case ◽  
Surgical Intervention ◽  
Anorectal Malformations ◽  
Colovesical Fistula ◽  
Surgical Practice ◽  
Life Threatening ◽  
Congenital Pouch Colon ◽  
Pouch Colon

Anorectal malformations are relatively common anomalies encountered in pediatric surgical practice. They are usually recognized at birth with absent anal canal or failure to pass meconium and hence can lead to life threatening bowel obstruction without surgical intervention. We are reporting a rare case of non-syndromic, sporadic, terminal colovesical fistula associated with high anorectal malformation not associated with congenital pouch colon in a neonate.

scholarly journals Whole exome-trio analysis reveals rare variants associated with Congenital Pouch Colon

2019 ◽  
Author(s):  
Sonal Gupta ◽  
Praveen Mathur ◽  
Ashwani Kumar Mishra ◽  
Krishna Mohan Medicherla ◽  
Prashanth Suravajhala
Keyword(s):  
Rare Variants ◽  
De Novo ◽  
Anorectal Malformations ◽  
Open Reading Frames ◽  
Missense Mutations ◽  
Clinical Genetic ◽  
Variants Of Unknown Significance ◽  
Whole Exome ◽  
Congenital Pouch Colon ◽  
Pouch Colon

AbstractAnorectal malformations (ARM) are individually common but Congenital Pouch Colon (CPC), a rare anorectal anomaly causes a dilated pouch in genitourinary tract. We have earlier attempted to understand the clinical genetic makeup of CPC and identified genes responsible for the disease using whole exome sequencing (WES). Here we report our studies of CPC, by identifying de novo heterozygous missense mutations in 16 proband-parent trios and further discover variants of unknown significance which could provide insights into CPC manifestation and its etiology. Our study confirms candidate mutations in genes, viz. C7orf57, C10orf120, C9orf84 and MUC16, CTC1 particularly emphasizing the role of hypothetical genes or open reading frames causing this developmental disorder. Variant validation revealed disease causing mutations associated with CPC and genitourinary diseases which could close the gaps of surgery in bringing intervention in therapies.

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