Noncommunicating isolated enteric duplication cyst in childhood

Srivastava, P. K.; Gangopadhyay, A. N.; Kumar, V.R. Ravi; Upadhyaya, Vijai D.; Sharma, Seema; Jaiman, Richa; Hasan, Zaheer

doi:10.1016/j.jpedsurg.2009.03.041

Cited by 38 publications

(40 citation statements)

References 7 publications

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“…Duplication cysts may be associated with malrotation, esophageal duplication and vertebral anomalies [5] and [9]. A cyst may be termed as a true duplication cyst if it fulfills the three criteria: attachment to any part of the gastrointestinal tract, lined by any gastrointestinal epithelium and containing smooth muscle in its wall [10]. It may be cystic or tubular.…”

Section: Discussionmentioning

confidence: 99%

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A Rare Cause of Intestinal Obstruction in Infants: Ileum Duplication Cyst

2017

IJSR

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Duplication cyst is a rare congenital anomaly presenting in pediatric patients that is most commonly seen in the ileum. It was first described by Wendel. Though they are more often observed in the small intestine, DCs can also more rarely be rectal, duodenal, gastric, and thoraco-abdominal. They have an incidence of 1/100,000. A 5 day old girl was admitted to our hospital for investigation of progressive abdominal distension and biliary vomiting. USG and CT-SCAN finding shows a large thin walled intra peritoneal welldefined cystic lesion occupying whole of the abdominal cavity. Microscopic examination of cyst shows features of enteric duplication cyst.

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Section: Discussionmentioning

confidence: 99%

“…They do not communicate with the bowel, but may share a common wall and blood supply. Tubular duplication cysts communicate with the intestinal lumen [10].…”

Section: Discussionmentioning

confidence: 99%

A Rare Cause of Intestinal Obstruction in Infants: Ileum Duplication Cyst

2017

IJSR

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“…It was located on the mesenteric border and shared a common wall with the normal ileum. [1] 1.5 cm diameter size of perforation was found in the antimesenteric border of the duplication with normal appendix (Fig. 1).…”

Section: Case Reportmentioning

confidence: 97%

Perforated Congenital Enteric Duplication Cyst Mimic as Appendicular Pathology: A Rare Case

Dakshnamoorthy¹

2016

jemds

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We report a case of perforated enteric duplication cyst, which was preoperatively diagnosed as appendicular mass. Duplication cysts are rare gastrointestinal congenital abnormalities and can occur anywhere within the gastrointestinal tract, may be located anywhere from the mouth to the anus. Signs and symptoms are dependent upon the location of the lesion. Perforated Enteric duplication mimic as appendicular pathology is a rare presentation in children.

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“…Non-communicating enteric duplications in the abdomen are extremely rare (Srivastava et al 2009;Kim et al 2013). We here report the case of a noncommunicating small intestine duplication that was described in a dog on the basis of sonographic, radiographic, gross and histopathological findings.…”

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confidence: 91%

“…Duplications of the alimentary tract are tubular or spherical structures lined by epithelium similar to intestine that are firmly attached to or share a wall of the alimentary tract (Srivastava et al 2009). The aetiological mechanism of enteric duplication is currently unknown.…”

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confidence: 99%

Non-communicating small intestinal duplication in a dog: a case report

Hwang¹,

Jung²,

Kim³

et al. 2017

Vet. Med. - Czech

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Enteric duplication is rare in dogs. Here, we report the rarest form of duplication in which two segments are parallel and share a wall for most of their lengths. A nine-year-old spayed female Yorkshire terrier was referred to the Veterinary Medical Teaching Hospital at Gyeongsang National University due to anorexia and diarrhoea. Physical examination, haematological examination, radiography, and ultrasonography were performed. On physical examination, dry, pale mucous membrane was identified. Moderate anaemia with decreased packed cell volume was detected in complete blood count. Serum urea nitrogen and creatinine levels were mildly increased. Radiographic images revealed no significant findings. On ultrasonographic examination, a multi-layered appearance of a focal small intestinal segment was identified in the left mid abdomen. Following the lesion, it was divided into two small intestinal segments. Based on imaging findings, intussusceptions or enteric duplication were suspected. To resect the abnormal small intestinal segment, enterectomy was performed. Follow-up was not performed because the patient expired during the postoperative recovery time. The histopathological diagnosis was non-communicating small intestinal duplication. Non-communicating intestinal duplication is related to embryologic abnormalities and is usually concurrent with other anomalies such as vertebral malformations and urogenital duplications. However, this case had no other anomalies associated with the malformation of the intestine.

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Noncommunicating isolated enteric duplication cyst in childhood

Cited by 38 publications

References 7 publications

A Rare Cause of Intestinal Obstruction in Infants: Ileum Duplication Cyst

A Rare Cause of Intestinal Obstruction in Infants: Ileum Duplication Cyst

Perforated Congenital Enteric Duplication Cyst Mimic as Appendicular Pathology: A Rare Case

Non-communicating small intestinal duplication in a dog: a case report

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