Duplication Cyst with Intestinal Volvulus Causing Intestinal Atresia/Stenosis in Neonates

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Intestinal Duplication Cyst Misdiagnosed as Meckel's Diverticulum

An intestinal duplication cyst is a very rare congenital anomaly, with symptoms including abdominal pain, abdominal distention, intestinal bleeding, and hematochezia. Hematochezia can be caused by ectopic gastric mucosa, although there are other causes of infantile hematochezia; hence, an intestinal duplication cyst can be misdiagnosed as bowel intussusception or Meckel's diverticulum. Here, a ...

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[Adult intestinal malrotation associated with intestinal volvulus].

BACKGROUND Intestinal malrotation is a congenital anomaly of the intestinal rotation and fixation, and usually occurs in the neonatal age. OBJECTIVE Description of a clinical case associated with acute occlusive symptoms. CLINICAL CASE A case of intestinal malrotation is presented in a previously asymptomatic woman of 46 years old with an intestinal obstruction, with radiology and surgical ...

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Enterogenous cyst causing congenital intestinal obstruction.

Cysts whose walls reproduce completely or incompletely the structure of gut, whether discovered in the wall of the gut, attached to the gut, or even more or less remote from the gut, must have been derived from the gut (Evans, 1929). They originate either in the vitello-intestinal tract or in diverticula normally found in the developing embryonal entoderm (Lewis and Thyng, 1908). One or more of...

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Intestinal volvulus, Midgut volvulus, Adults

Introduction: Rotation of the small bowel around its mesenteric vascular pedicle is termed midgut volvulus. This abnormality frequently causes obstruction and, most importantly, compromises the intestinal blood flow, threatening bowel viability. Midgut volvulus can be primary without findings of any associated underlying cause, or secondary to other congenital or acquired conditions. Primary mi...

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Intestinal duplication cyst associated with intestinal malrotation anomaly: report of a case.

Duplications of the alimentary tract are rare congenital malformations and may occur anywhere in the intestinal tract. Intestinal duplication cysts have been rarely found with intestinal malrotation anomaly. We present a 2-year old boy who had intestinal duplication cyst, associated with intestinal malrotation anomaly.

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ژورنال

عنوان ژورنال: Journal of Neonatal Surgery

سال: 2018

ISSN: 2226-0439

DOI: 10.21699/jns.v7i4.820