Type 5 congenital pouch colon and its embryopathogenesis
نویسندگان
چکیده
منابع مشابه
Congenital Pouch Colon
(This section is meant for residents to check their understanding regarding a particular topic) QUESTIONS 1. What are the diagnostic features of congenital pouch colon (CPC)? 2. What associated anomalies are seen with congenital pouch colon? 3. What are various surgical options in the emergency management of congenital pouch colon? 4. What specific post-colostomy complications are seen with con...
متن کاملCongenital pouch colon - Then and now
Congenital pouch colon (CPC), a condition associated with anorectal agenesis has been reported mainly from the Indian subcontinent though there have been few case reports from other areas. The pouch differs from a normal colon structurally, histologically and functionally. The management involves a diversion colostomy at birth with or without the excision of pouch followed by pull through. This...
متن کاملCongenital Pouch Colon with Double Meckel’s Diverticulae
A one-day-old boy weighing 2.4 kg was admitted with imperforate anus. On physical examination there was marked abdominal distension and palpable bladder. External genitalia were normal. A per urethral 6F feeding tube could be passed easily into the bladder. Invertogram suggested the presence of congenital pouch colon malformation. Exploration revealed type 1 complete colonic pouch and a bladder...
متن کاملCongenital Pouch Colon with Unilateral Renal Agenesis and Monorchism
BACKGROUND Congenital pouch colon, also known as congenital short colon or "Pouch colon syndrome", is a rare condition that occurs in association with anorectal malformations; colon is either partially or completely replaced by pouch-like dilatation and communicates with the urogenital tract by means of a fistula. This anomaly is exclusively seen in Northern parts of India with only a few cases...
متن کاملType V Pouch Colon, Prune Belly Syndrome, and Congenital Anterior Urethrocutaneous Fistula
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).
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ژورنال
عنوان ژورنال: Medical Journal of Dr. D.Y. Patil Vidyapeeth
سال: 2018
ISSN: 2589-8302
DOI: 10.4103/mjdrdypu.mjdrdypu_17_18