Congenital jejunal stenosis and gastric duplication cysts are very rare congenital anomalies of the gastrointestinal tract in the newborn. We present a case of congenital membranous jejunal stenosis associated with gastric duplication cysts, which was diagnosed by ultrasonography. To the best of our knowledge, this is the first report of ultrasonographic diagnosis of congenital membranous jejunal stenosis associated with a gastric duplication cyst in a newborn.
Case presentation
A 1-month-old Chinese baby girl presented with projectile vomiting and hyperpyrexia for 3 days. An upper gastrointestinal contrast study showed incomplete duodenal obstruction; however, ultrasonography revealed congenital membranous jejunal stenosis associated with a gastric duplication cyst. After surgical excision of the jejunal membrane and gastric duplication cyst, she recovered well with no bilious vomiting at the 1-year follow-up.
Conclusion
Ultrasonography is a useful tool for the evaluation of membranous jejunal stenosis and the identification of small, asymptomatic gastrointestinal duplication cysts.
Hinweise
Competing interests
The authors declare that they have no competing interests.
Authors’ contributions
LQ performed the ultrasonographic examination of the case, and was a major contributor in writing the manuscript. WS obtained the relevant literature. LX collected the patient’s clinical data. ZX and ML translated and proofread the manuscript in English. All authors read and approved the manuscript.
Abkürzungen
GI
Gastrointestinal
Introduction
Congenital jejunal stenosis and gastric duplication cysts are very rare congenital anomalies of the gastrointestinal (GI) tract in the newborn; the prevalence rate of jejunoileal atresia and stenosis has been reported to be between 1 in 330 and 0.9 in 10,000 live births, and stenosis occurs in 7 % of cases [1]. The incidence of duplication cysts of the alimentary system is approximately 1 in 4500 live births [2], and gastric duplication cysts represent only 4 to 5 % of these cases [3, 4]. We present a case of congenital membranous jejunal stenosis associated with gastric duplication cysts, which was diagnosed by ultrasonography. The patient underwent surgery and recovered well. To the best of our knowledge, this is the first report of ultrasonographic diagnosis of congenital membranous jejunal stenosis associated with a gastric duplication cyst in a newborn.
Case presentation
A 1-month-old Chinese baby girl presented to our emergency department with vomiting and high-grade fever, which had occurred for 3 days. The fever was not associated with rigors and chills. She presented with a history of intermittent projectile and bilious vomiting after breastfeeding. Vomiting occurred approximately five times each day, at a volume of 10mL at each instance. A general physical examination revealed a temperature of 39 °C, pulse rate of 100/minute, and respiratory rate of 30/minute. On abdominal examination, no abdominal distention, regional tenderness, or rebound was observed, and no masses or viscera could be palpated. Bowel sounds were audible, and other physical examination results were normal. An upper GI contrast study in another hospital showed incomplete duodenal obstruction (Fig. 1). However, to clarify the cause of intestinal obstruction, she subsequently underwent ultrasonographic examination after hospitalization. Ultrasonography showed continuous opening of the pylorus and significant dilatation of her duodenum; her upper jejunum in the left abdomen was approximately 4cm in diameter, and we observed frequent reverse peristalsis. An intraluminal membrane was visible in the dilated distal jejunum site (Fig. 2), and the “billow” in the proximal jejunum could be seen to intermittently move in and out of a pinhole in the mucosal diaphragm. The distal intestine was deflated, and there was an absence of gas; by ultrasonography, a diagnosis of congenital membranous jejunal stenosis was considered. Furthermore, an ultrasound showed a cystic structure sized 2.0 × 1.5cm in the greater curvature in the left hypochondrium (Fig. 3). It was firmly attached at the gastric wall, and the cyst walls consisted of an inner echogenic rim and an outer echogenic rim area. The central area was hypoechoic. A gastric duplication cyst was considered the most likely diagnosis, and a laparotomy was planned after initial stabilization. During surgery, jejunal stenosis situated approximately 15cm from the ligament of Treitz and a diaphragm with a pinhole in the intestinal cavity was found and resected. In addition, surgical excision of the cyst located on the greater curvature of the stomach was performed. A histopathological examination revealed that both sides of the resected intestinal membrane were covered with intestinal mucosa (Fig. 4) and the structure of the gastric mucosa and smooth muscles in the wall of the cyst, confirming the diagnosis of membranous jejunal stenosis and gastric duplication cyst (Fig. 5). Postoperative recovery was uneventful, and she was discharged on the ninth day following surgery. She recovered well with no bilious vomiting at the 1-year follow-up.
Fig. 1
Upper gastrointestinal contrast study showing marked dilatation of the duodenum
Fig. 2
Ultrasonography showing dilatation of the duodenum and proximal jejunum. A membrane (arrow) and a pinhole (small arrowhead) are seen in the jejunal membrane
Fig. 3
Ultrasonographic image of the gastric duplication cyst. It was 1.5 × 1.4cm and intimately attached at the greater curvature of the stomach
Fig. 4
Histopathological examination showing both sides of the resected intestinal membrane covered with intestinal mucosa
Fig. 5
Histological examination of the resected cyst. Gastric mucosa and smooth muscles are seen in the wall of the cyst
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Discussion
In general, the symptoms of patients with congenital anomalies of the alimentary tract present early after birth with recurrent, progressive vomiting. Bilious vomiting indicates obstruction distal to the ampulla of Vater [5], which requires an immediate and correct diagnosis and surgical correction to avoid serious complications. Normally, within 3 hours of birth, the entire small bowel contains gas, whereas gas is observed in the sigmoid colon 8 to 9 hours after birth [6]. In some patients with congenital anomalies of the GI tract causing obstructions, the proximal bowel with lesions exhibits dilatation and effusion, and the distal intestinal cavity has little or no gas, thereby creating favorable conditions for ultrasonic detection of the lesions. Furthermore, ultrasonography of the GI tract is noninvasive, simple, radiation-free, and fairly accurate for the diagnosis of GI obstruction. Therefore, ultrasonography plays a vital role in the evaluation of patients with congenital anomalies of the GI tract. Ultrasonography has been used as an alternative to barium studies in diagnosing certain congenital anomalies of the GI tract, including annular pancreas, hypertrophic pyloric stenosis, enteric duplication cysts, malrotation, and midgut volvulus [5]. However, the use of ultrasonography for the detection and diagnosis of membranous jejunal stenosis has not been previously reported in the literature. A previous study reported that jejunoileal atresia and stenosis are difficult to evaluate [7]. In the present case, ultrasonography revealed the mucosal diaphragm with a pinhole in the jejunum, the duodenum and proximal jejunum loops significantly dilated with fluid, and the distal small intestine deflated with little gas. Based on this case, ultrasonography may have greater importance in the evaluation of membranous jejunal stenosis, as it enables the distinction from atresia and provides excellent anatomic details for correct diagnosis and treatment planning.
Duplication cysts are rare congenital anomalies that can occur in any part of the GI tract, although the most common site is the ileum [3]. Gastric duplication cysts represent only 4 to 5% of duplication cysts and are located along the greater curvature of the stomach, usually in the antrum [3, 4]. Possible causes of gastric duplication cysts include errors in recanalization of the alimentary tract, McLetchie’s theory of traction diverticulum formation caused by endo-ectodermal adhesions, split notochord, and partial twinning [8, 9]. On clinical examination, gastric duplication cysts can present with vague abdominal pain, vomiting, and occasionally a palpable abdominal mass; however, presentation is usually asymptomatic and therefore difficult to diagnose [10]. In the present case, a gastric duplication cyst was incidentally diagnosed by abdominal ultrasonography. Ultrasonography showed a small cystic lesion on the greater curvature of the stomach in the left hypochondrium. Characteristic ultrasonographic features of a GI duplication cyst are a hypoechoic muscular rim surrounding an echogenic mucosa; these features are specific to gastric duplication cysts and are not seen with other cystic lesions [11]. However, in the present case, an upper GI tract contrast study was performed, with no evidence of mass lesions. This case report illustrates the important role of ultrasonography in detecting small, unsuspected duplication cysts.
Conclusions
Using ultrasonography, we successfully diagnosed congenital membranous jejunal stenosis associated with a gastric duplication cyst in a newborn. This case emphasizes that ultrasonography in a baby with congenital jejunal stenosis was effective as a diagnostic modality. In addition, ultrasonography can be helpful for the accurate identification of small and asymptomatic GI duplication cysts. Ultrasonography is superior to radiography for revealing the cause of some intestinal obstructions, suggesting that babies with bilious vomiting should have a routine ultrasound for diagnosis.
Consent
Written informed consent was obtained from the patient’s legal guardian for publication of this case report and accompanying images. A copy of the written consent is available for review by the Editor-in-Chief of this journal.
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Acknowledgments
We are very grateful to our supervisor, Editage, and Dr Zheng Wenhui, who provided valuable guidance at every stage of the writing of this report.
This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
Competing interests
The authors declare that they have no competing interests.
Authors’ contributions
LQ performed the ultrasonographic examination of the case, and was a major contributor in writing the manuscript. WS obtained the relevant literature. LX collected the patient’s clinical data. ZX and ML translated and proofread the manuscript in English. All authors read and approved the manuscript.
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