Isolated Jejunal Duplication Cyst Associated with Intestinal Malrotation in a Newborn
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چکیده
منابع مشابه
Isolated Jejunal Duplication Cyst Associated with Intestinal Malrotation in a Newborn
Alimentary tract duplications are epithelial-lined cystic or tubular structures attached to bowel wall and supplied by mesenteric vessels. Association between intestinal malrotation and duplication cyst, especially of jejunal location is rarely mentioned in literature [1-5]. We are reporting a rare coexistence of isolated jejunal duplication cyst and malrotation in a neonate with intestinal obs...
متن کاملIntestinal 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.
متن کاملIntestinal Obstruction due to Ileal Duplication Cyst and Malrotation in a Preterm Neonate
The baby was born to a 24-year-old primigravida mother by cesarean section at 36 week gestation and weighed 2420 grams. Antenatal scan at 32 week gestation showed dilated bowel loops and polyhydramnios (Amniotic fluid index: 32 cm) suggestive of intestinal obstruction. He developed respiratory distress soon after birth and was referred to our unit. On examination, the baby had respiratory distr...
متن کامل[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 ...
متن کاملThoraco-abdominal enteric duplication cyst in association with neurenteric cyst, axial skeletal anomalies, and malrotation
We report a case of a 2-year old boy with cervicothoracic deformity with vertebral rib anomalies, neurenteric cyst, separate thoracoabominal enteric duplication cyst, concurrent intestinal malrotation, and dextroposition of the heart. This combination of abnormalities is very rare. When these lesions are suspected, the patient must be investigated carefully. This case is presented to show the i...
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ژورنال
عنوان ژورنال: Journal of Neonatal Surgery
سال: 2016
ISSN: 2226-0439
DOI: 10.21699/jns.v5i4.455