scholarly journals Jejunal Windsock Deformity: A Rare Cause of Incomplete Neonatal Intestinal Obstruction

2016 ◽  
Vol 5 (4) ◽  
pp. 57
Author(s):  
Vijai Datta Upadhyaya ◽  
Basant Kumar ◽  
Amrit Gupta ◽  
Kirti Narangane ◽  
Anita Singh

Incomplete intestinal obstruction due to windsock web of the jejunum is uncommonly notice in neonates. We present a male neonate, prenatally suspected case of proximal bowel obstruction, who was found to have features of incomplete intestinal obstruction due to windsock deformity in jejunum. The difficulty in the diagnosis and management is discussed along with relevant literature review.

2016 ◽  
Vol 5 (4) ◽  
pp. 58 ◽  
Author(s):  
Elias Chamely ◽  
Brice Antao

Congenital mesocolic hernia is an extremely rare, but serious cause of intestinal obstruction in children. Given the rarity of this condition, delays in diagnosis and management can have catastrophic consequences. Congenital mesocolic hernias are usually caused by an abnormal rotation of primitive mid-gut and are divided into left and right congenital mesocolic hernias. We report and discuss the clinical and radiological features and management of a neonate with an extremely rare variant, congenital middle mesocolic hernia along with a literature review of this rare condition.


2019 ◽  
Vol 12 (8) ◽  
pp. e230253
Author(s):  
Kanika Sharma ◽  
Anjan Dhua ◽  
Deena Thomas ◽  
Mari Jeeva Sankar

Internal herniation through congenital sigmoid mesocolic defect as a cause of neonatal intestinal obstruction is rarely reported. Clinical judgement combined with judicious use of investigations and prompt exploration is essential to provide immediate relief of the obstruction and salvage the herniated loop of bowel, which otherwise might lead to morbidity and even death. We present a neonate with internal herniation of the ileum through a congenital mesocolic defect which was diagnosed by a prompt abdominal exploration in view of persistent clinical signs of intestinal obstruction. The relevant literature is also discussed highlighting the rarity of neonatal presentation of sigmoid mesocolic defect.


2016 ◽  
Vol 7 (2) ◽  
pp. 130-135
Author(s):  
Mary Worthen ◽  
Swapna Chandran

ABSTRACT Background The prevalence of pediatric dysphonia ranges from 6-23%. Chronic dysphonia can negatively affect the lives of children physically, socially, and emotionally. The body of literature continues to grow regarding the pathophysiology and management of dysphonic children. Methods This article presents a relevant literature review of vocal fold pathology leading to hoarseness and recent advances in diagnosis and management. Articles were retrieved using a selective search in PubMed employing the terms such as “hoarseness in children,” “pediatric dysphonia.” Results 42 articles from the past decade were reviewed that include information regarding the etiology, assessment, and treatment of children with dysphonia. Conclusion The care of a child with a voice disorder can be complex and requires a multi-disciplinary approach. Current technological, pharmaceutical, and therapeutic advances have improved the treatment of children with dysphonia. How to cite this article Worthen M, Chandran S. Hoarseness in Children. Int J Head Neck Surg 2016;7(2):130-135.


2021 ◽  
Vol 07 (03) ◽  
pp. e209-e211
Author(s):  
Charif Khaled ◽  
Michel Akl ◽  
Toufic Moussallem

AbstractThis study depicts the case of a young female presenting with intestinal obstruction. Surgery uncovered a small bowel hamartoma that has caused a transmesenteric internal hernia and volvulus. As far as we know, this is unheard of before, as all three mentioned entities are very rare. The study also covers a literature review of cases of internal hernia with volvulus and stresses over the need for urgent diagnosis and management.


1989 ◽  
Vol 16 (1) ◽  
pp. 85-96 ◽  
Author(s):  
Hernan M. Reyes ◽  
Janet L. Meller ◽  
Deborah Loeff

2021 ◽  
Author(s):  
Mostafa Kotb ◽  
Ahmed Aboelela ◽  
Ahmed Eshiba ◽  
Eman Sheta ◽  
Dina Abdallah

2021 ◽  
Vol 49 (2) ◽  
pp. 030006052199223
Author(s):  
Xiaolin Zhang ◽  
Hongmei Jiao ◽  
Xinmin Liu

Esophageal diverticulum with secondary bronchoesophageal fistula is a rare clinical entity that manifests as respiratory infections, coughing during eating or drinking, hemoptysis, and sometimes fatal complications. In the present study, we describe a case of bronchoesophageal fistula emanating from esophageal diverticulum in a 45-year-old man who presented with bronchiectasis. We summarize the characteristics of this rare condition based on a review of the relevant literature.


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