scholarly journals Congenital pouch colon with colonic atresia- An unusual embryological association: A case report

2021 ◽  
Vol 10 ◽  
pp. 33
Author(s):  
Praveen Mathur ◽  
Sharanabasappa Gubbi ◽  
Aadil Farooq ◽  
Priyanka Mittal ◽  
Gunjan Sharma
Keyword(s):  
Case Report ◽  
Anorectal Malformation ◽  
English Literature ◽  
Abdominal Distension ◽  
Case Presentation ◽  
Male Baby ◽  
Colonic Atresia ◽  
Congenital Pouch Colon ◽  
Pouch Colon

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.

scholarly journals Feasibility of primary anastomosis for right-sided colonic atresia: A case report

2021 ◽  
Vol 10 ◽  
pp. 46
Author(s):  
Muhammad Shamil Suhaimi ◽  
Mohd Yusran Othman ◽  
Khalilah Alhuda Kamilen
Keyword(s):  
Case Report ◽  
Primary Anastomosis ◽  
Distal Colon ◽  
Postoperative Recovery ◽  
Ascending Colon ◽  
Case Presentation ◽  
Male Baby ◽  
Colonic Atresia ◽  
Feasible Option

Background: Colonic atresia (CA) is a rare cause of congenital intestinal obstruction. The management of CA is challenging because of its rarity. Case Presentation: We present a case of right-sided CA in a term male baby weighing 3006 gm, without any other comorbidity. Type 1 atresia was seen at ascending colon and upon decompression, a reasonable caliber was achieved for a primary anastomosis following distal Cheatle slit and proximal tapering. Postoperative recovery was uneventful. Conclusion: Primary anastomosis is a feasible option in right-sided CA when no major comorbidity is present and a normal distal colon with reasonable caliber is certain.

Descending Cervical-Sacral Pain after the Administration of Antivenom to the Scorpion Sting Poisoning: A Case Report

2020 ◽  
Vol 2 (2) ◽  
pp. 93-96
Author(s):  
Josué Saúl Almaraz Lira ◽  
Alfredo Luis Chávez Haro ◽  
Cristian Alfredo López López ◽  
Remedios del Pilar González Jiménez
Keyword(s):  
Blood Pressure ◽  
Type 2 Diabetes ◽  
Case Report ◽  
Signs And Symptoms ◽  
Cervical Region ◽  
Scorpion Sting ◽  
Case Presentation ◽  
Sacral Region ◽  
Scorpion Stings

Introduction. Scorpion stings occur mainly in spring and summer, with an estimate of 1.2 million cases per year worldwide. About 300,000 poisonings occur within a year, primarily affecting children and adults older than 65 years. In 2019, Guanajuato (Mexico) ranked third in poisoning by scorpion sting with a total of 43,913 cases. The intoxication grades are three where the signs and symptoms are varied. There are two types of antivenom in the Mexican market, and we use Alacramyn® in our case. Case presentation. A 70-year-old female —with grade 1 scorpion sting poisoning, 30 minutes of evolution, with type 2 diabetes and high blood pressure— received two vials of antivenom according to current regulations. She presented transient vagal reaction and subsequent transient pain in the cervical region that radiates to the sacral region. At discharge, there are no data compatible with scorpion sting poisoning. Conclusions. Transient pain in the cervical region to the sacral region may be secondary to an anxiety crisis, hypersensitivity to IgG, or secondary reaction to administration in less time than recommended by the provider. The benefit was greater than the reactions that occurred.

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
Keyword(s):  
Intestinal Obstruction ◽  
Anorectal Malformation ◽  
Developmental Anomaly ◽  
Abdominal Radiograph ◽  
Abdominal Drain ◽  
The Third ◽  
Neonatal Intestinal Obstruction ◽  
Segmental Dilatation ◽  
Congenital Pouch Colon ◽  
Pouch Colon

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.

A Female Patient with Congenital Pouch Colon (CPC): a Case Report

2011 ◽  
Vol 111 (5) ◽  
pp. 335-337 ◽  
Author(s):  
O. Yilmaz ◽  
A. Genc ◽  
S. Ayhan ◽  
T. Ozcan ◽  
R. Aygoren ◽  
...  
Keyword(s):  
Case Report ◽  
Female Patient ◽  
Congenital Pouch Colon ◽  
Pouch Colon

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 Congenital pouch colon associated with anorectal malformation: A rare anomaly of Asian Region – Experience of kurdish centre

2018 ◽  
Vol 15 (1) ◽  
pp. 10
Author(s):  
Rossella Angotti ◽  
QadirQadir Mohamed Salih ◽  
Francesco Molinaro ◽  
Francesco Ferrara ◽  
Marina Sica ◽  
...  
Keyword(s):  
Anorectal Malformation ◽  
Asian Region ◽  
Rare Anomaly ◽  
Congenital Pouch Colon ◽  
Pouch Colon

scholarly journals Acquired colonic atresia in a 4-month old term male infant: a rare case report

2017 ◽  
Vol 4 (2) ◽  
pp. 669
Author(s):  
Kamal Nain Rattan ◽  
Gurupriya J. ◽  
Shruti Bansal ◽  
Rohit Kapoor ◽  
Roomi Yadav
Keyword(s):  
Case Report ◽  
Necrotizing Enterocolitis ◽  
Rare Case ◽  
Male Infant ◽  
Abdominal Distension ◽  
Exploratory Laparotomy ◽  
Inflammatory Mass ◽  
Colonic Atresia ◽  
Rare Case Report ◽  
History Of

Acquired colonic atresias are very rare but, are known in association with necrotizing enterocolitis. We report a case of a 4-month term male infant with recurrent episodes of abdominal distension, bilious vomiting and constipation off and on, without the history of necrotizing enterocolitis. Exploratory laparotomy was performed, an inflammatory mass with multiple dense interloop adhesions were found in the mid-transverse colon. These adhesions were lysed to identify the proximal dilated and distal blind end of the colon.  Rest of the gut was normal.  This case is unique for the fact that, it is a case of acquired colonic atresia without history of necrotizing enterocolitis, unlike other reported cases of acquired colonic atresia.

scholarly journals Congenital pouch colon: A rare presentation of Anorectal malformation

2015 ◽  
Vol 57 (3) ◽  
pp. 193-197 ◽  
Author(s):  
Salah S. Mahmood ◽  
◽  
Ahmed Z. Zain ◽  
Raghad J. Aboalhab ◽  
◽  
...  
Keyword(s):  
Anorectal Malformation ◽  
Rare Presentation ◽  
Congenital Pouch Colon ◽  
Pouch Colon
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