Situs inversus in association with duodenal atresia

Talabi, Ademola Olusegun; Sowande, Oludayo Adedapo; Tanimola, Adebayo Gbenga; Adejuyigbe, O

doi:10.4103/0189-6725.120896

Cited by 10 publications

(15 citation statements)

References 7 publications

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“…Due to the incomplete obstruction of the duodenum, CDS often has a delayed presentation, which makes a diagnosis difficult [2–4]. A fluid diet like milk can pass through the duodenal stenosis but not solid food.…”

Section: Discussionmentioning

confidence: 99%

“…Congenital duodenal obstruction associated with SI is an extremely rare condition, and only about 20 patients have been reported in the literature [2, 6, 7]. In particular, only a few CDS patients associated with SI have ever been reported before [2].…”

Section: Discussionmentioning

confidence: 99%

“…In particular, only a few CDS patients associated with SI have ever been reported before [2]. Although there are some reports of gastroscopic treatment for membranous duodenal stenosis, we selected open surgery because the location of the papilla Vater could not be identified in our case [5, 8].…”

Section: Discussionmentioning

confidence: 99%

“…The surgical procedures for SI patients are technically challenging because of the mirror image anatomical construction and high frequency of other anomalies. Congenital duodenal obstruction, which includes atresia and stenosis, is estimated to have an incidence of about 1 in 4,000 to 15,000 live births [2, 3]. Congenital duodenal stenosis (CDS) is relatively rare in comparison with duodenal atresia and sometimes has a delayed presentation [3–5].…”

Section: Introductionmentioning

confidence: 99%

“…Congenital duodenal stenosis (CDS) is relatively rare in comparison with duodenal atresia and sometimes has a delayed presentation [3–5]. CDS associated with SI is an extremely rare entity and only a few cases have been reported thus far [2, 6]. We present a case of a 1-year-old girl with CDS and SI who successfully underwent a transumbilical radical operation as minimally invasive surgery.…”

Section: Introductionmentioning

confidence: 99%

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Transumbilical Surgery for Duodenal Stenosis in a Child with Situs Inversus: The First Report

Saeki

Ueno²,

Mukai³

et al. 2017

Case Reports in Pediatrics

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Background. Situs inversus is a rare congenital anomaly with a reported incidence of only 1 in 5,000 to 10,000 live births. Congenital duodenal stenosis complicated with situs inversus is an even rarer entity. Case Presentation. A 1-year-old girl with situs inversus who had undergone a hemi-Fontan procedure against a single ventricle in our hospital was referred to our department for vomiting and failure to thrive. An upper gastrointestinal contrast study and endoscopy revealed duodenal stenosis. A transumbilical radical operation as a minimally invasive surgery was successfully performed. After the surgery, she stopped vomiting, and the postoperative course was uneventful with good cosmetic results. Conclusions. To our knowledge, this is the first report of transumbilical surgery for congenital duodenal stenosis with situs inversus as minimally invasive surgery. Transumbilical surgery to situs inversus patient can be performed safely and lead to good cosmetic outcome.

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Section: Discussionmentioning

confidence: 99%

Section: Discussionmentioning

confidence: 99%

Section: Discussionmentioning

confidence: 99%

Section: Introductionmentioning

confidence: 99%

Section: Introductionmentioning

confidence: 99%

See 3 more Smart Citations

Transumbilical Surgery for Duodenal Stenosis in a Child with Situs Inversus: The First Report

Saeki

Ueno²,

Mukai³

et al. 2017

Case Reports in Pediatrics

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Features, genetics and their correlation in Jalili syndrome: a systematic review

et al. 2019

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Jalili syndrome is a rare genetic disorder first identified by Jalili in Gaza. Amelogenesis imperfecta and cone-rode dystrophy are simultaneously seen in Jalili syndrome patients as the main and primary manifestations. Molecular analysis has revealed that the CNNM4 gene is responsible for this rare syndrome. Jalili syndrome has been observed in many countries around the world, especially in the Middle East and North Africa. In the current scoping systematic review we searched electronic databases to find studies related to Jalili syndrome. In this review we summarise the reported clinical symptoms, CNNM4 gene and protein structure, CNNM4 mutations, attempts to reach a genotype-phenotype correlation, the functional role of CNNM4 mutations, and epidemiological aspects of Jalili syndrome. In addition, we have analysed the reported mutations in mutation effect prediction databases in order to gain a better understanding of the mutation’s outcomes.

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Situs Inversus Totalis, Polysplenia and Annular Pancreas with Duodenal Obstruction: a Case Report of Bizarre Embryological Conundrum

2020

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Situs inversus, polysplenia and annular pancreas are unusual anomalies individually, and are extremely rare in combination. A 3 years old boy presented with failure to thrive and symptoms of chronic upper gastrointestinal obstruction. After adequate radiological investigations, he was explored and managed with a duodeno-duodenostomy. and is doing well on a 1 year follow-up. The preoperative radiological assessment is of paramount importance, so as to avoid any intra-operative surprises.

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Situs inversus in association with duodenal atresia

Cited by 10 publications

References 7 publications

Transumbilical Surgery for Duodenal Stenosis in a Child with Situs Inversus: The First Report

Transumbilical Surgery for Duodenal Stenosis in a Child with Situs Inversus: The First Report

Features, genetics and their correlation in Jalili syndrome: a systematic review

Situs Inversus Totalis, Polysplenia and Annular Pancreas with Duodenal Obstruction: a Case Report of Bizarre Embryological Conundrum

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