scholarly journals Esophagus atresia and duodenal obstruction: report of two cases

2020 ◽  
Vol 10 (3) ◽  
Author(s):  
Júlio Tavares ◽  
Mauro Basso ◽  
Andrea Miyasaki ◽  
Ricardo Parreira ◽  
Heloisa Menezes

Esophageal atresia, with or without tracheoesophageal fistula, and congenital duodenal obstructions are relatively frequent changes in the digestive tract in pediatric surgery. The combination of both, although described in the literature, is unusual. It is assumed that the early diagnosis with imaging tests and the combined surgical schedule, although still undefined, can reduce the mortality of these children. We report the cases of two newborns with esophageal atresia and congenital duodenal obstruction, concerning diagnosis, surgical treatment and clinical evolution.

2018 ◽  
Vol 7 (2) ◽  
pp. 23
Author(s):  
Shailesh Solanki ◽  
Ravi Prakash Kanojia ◽  
Ram Samujh

Esophageal atresia with tracheoesophageal fistula (EA-TEF) is a well-known congenital anomaly and Type C variety of gross classification is the most common. Even for Type C variety, anatomy of upper pouch and lower pouch is not always the same. We are presenting three cases of Type C EA-TEF with unusual anatomy. In this type, upper pouch crosses over the lower pouch for a significant length. The cases are described here to highlight this variant of Type C EA-TEF which produces diagnostic dilemma. An early diagnosis of this variant, prevents morbidity and mortality.


2021 ◽  
Vol 100 (6) ◽  
pp. 45-53
Author(s):  
I.N. Khvorostov ◽  
◽  
N.K. Barova ◽  
S.V. Minaev ◽  
M.A. Akselrov ◽  
...  

The combination of duodenal atresia (DA) with esophageal atresia with tracheoesophageal fistula (EA-TEF) is a rare pathology, the frequency of which ranges from 1% to 6% of all cases of EA. Surgical treatment of the DA+EA-TEF combination always causes significant difficulties, primarily in determining the timing and stages of surgical correction. Objective of the study: to evaluate the results of treatment with a combination of DA+EA-TEF to determine the effective tactics of surgical treatment. Materials and methods of research: a retrospective, nonrandomized, uncontrolled, multicenter study was carried out. The work is based on the results of treatment of 15 newborns – 6 (40%) boys, 9 (60%) girls with a combination of DA+EA-TEF, who were treated in clinics of 6 university centers for pediatric surgery in the Russian Federation in 2015–2021. Simultaneous operations (SIMOPs) were performed in 10 (60%) patients, two-stage operations (TO) – in 5 (40%) newborns. The following criteria were taken into account: the period of antenatal (weeks) and postnatal (days) of establishing the diagnosis of obstruction of the gastrointestinal tract (GIT), gestational age (weeks), birth weight (g), weight at the time of surgery (g), type of concomitant pathology , sequence and methods of surgical treatment, terms of complete enteral feeding (days), outcomes of operations and reasons for unsatisfactory outcomes. The average gestational age of children who underwent SIMOPs was 35.1 weeks. (Q1 – 31.5, Q3 – 39; Me – 37; SD – 5.1; min/max – 25–40; 95% CI: 31.1–39.0) versus 29.8 weeks. at DO (Q1 – 29, Q3 – 30.5; Me – 30; SD – 1.0; min/max – 28–31; 95% CI: 28.4–31.6) did not differ statistically significantly (р=0.083). The mean body mass values did not have statistically significant differences (p=0.081) and amounted to 2224 g (Q1 – 1410, Q3 – 2930; Me – 2665; SD – 890.8; min/max – 760–3260; 95% CI: 1556–2926) for SIMOPs, versus 1322 g (Q1 – 1165, Q3 – 1450; Me – 1380; SD – 196; min/max – 980–1450; 95% CI: 1078.4–16565) in the TO group. Results: the average duration of SIMOPs was on average 144.4 min (Q1 – 125, Q3 – 155; Me – 147.5; SD – 22; min/max – 120–190; 95% CI: 1321–159.3), TO – 147.0 (Q1 – 125, Q3 – 172; Me – 140; SD – 33.4; min/max – 120–205; 95% CI: 126–178.6). The sequence of surgical correction of defects in SIMOPs in 8 (53%) patients consisted of thoracotomy, ligation of the TEF, direct anastomosis of the esophagus and the imposition of duodeno-duodenoanstomosis (DDA). In one case, DDA was selected as the first operation, which was supplemented with Kader gastrostomy followed by thoracotomy, ligation of the TEF and anastomosis of the esophagus after elongation according to I. Livaditis. In one patient, after thoracotomy and ligation of the TEF in connection with an insurmountable diastasis of the esophagus, a cervical esophagostomy (CE), duodenojejunoanastomosis (DEA) and a gastrostomy according to Kader were applied. In a two-stage correction (TO), the first operation in 3 patients was DDA (20%), supplemented in one case (7%) with Kader gastrostomy, and the second stage after 2 days performed thoracotomy with the elimination of TEF and EA. In 2 (13%) newborns, the first stage was thoracotomy, elimination of TEF and EA, followed by imposition of DDA 2 days later. In one case, due to an insurmountable diastasis of the esophagus after thoracotomy and ligation of the TEF, intrathoracic elongation of the esophagus according to Foker with delayed anastomosis of the esophagus (on the 7th day) and laparoscopic fundoplication according to Nissen (at 5 months) were performed. The duration of hospitalization did not statistically significantly depend on the chosen method for correcting the combination of DA+EA-TEF (p=0.79) and averaged 28.4 days for SIMOPs (Q1 – 16, Q3 –34.5; Me – 26; SD – 21.4; min/max – 5.0–79; 95% CI: 17.6–42.4), and for TOs – 27,2 days (Q1 – 21, Q3 – 33; Me – 28; SD – 7.1; min/max – 19–38; 95% CI: 27.2–33). In the group of patients with SIMOPs, 2 deaths (13%) were recorded on the 5th and 7th days after surgery due to progressive multiple organ failure and intractable pulmonary hypertension. In one case (7%), a lethal outcome was recorded 8 months after primary surgery due to progressive cardiovascular failure. Early postoperative mortality after SIMOPs was 20%, overall mortality was 30%. In the TO group, 3 (20%) deaths were recorded: 2 in the early postoperative period (on day 3 and day 19) and one at the age of 3 months of life. Early postoperative mortality after TO was 40%, overall mortality – 60%. Conclusion: it is preferable to choose the ligation of the TEF as the first operation and, if the child's condition allows, to impose an esophageal anastomosis and restore duodenal patency, followed by a nasogastric tube through the esophageal anastomosis into the stomach. If, after ligation of the TEF, the patient's cardiorespiratory status does not stabilize, it is possible to restore the patency of the esophagus and pass the probe into the stomach without imposing a gastrostomy, which will allow the patient to be further treated as an isolated DA, and the operation to restore the patency of the duodenum is delayed. In the presence of insurmountable diastasis, the use of esophageal elongation technology with subsequent delayed EA is justified.


2021 ◽  
pp. 097321792110406
Author(s):  
Nasreen Banu ◽  
VVS Chandrasekharam ◽  
Durga Prasad Koduru

Tracheoesophageal fistula (TEF) without associated esophageal atresia is a rare congenital anomaly. Diagnosis in neonatal period is usually not made and most of the patients are treated as cases of pneumonia. We report a case of H-type TEF, which was initially diagnosed as grade V gastroesophageal reflux on contrast esophagogram and bronchoscopy done revealed H-type fistula. Through cervical approach, fistula was repaired and baby had uneventful postoperative outcome. High index of clinical suspicion and early diagnosis can provide a better prognosis.


2019 ◽  
Vol 32 (Supplement_1) ◽  
Author(s):  
T Soyer ◽  
E Birben ◽  
Ö U Soyer ◽  
Ö B Türer ◽  
F Tunçer ◽  
...  

Abstract Aim MicroRNAs (miRNAs) are noncoding RNAs that play a role in regulation of inflammation and cancer. It has been shown that miRNA-21 and 24 are downregulated in the exhaled breath condensate (EBC) of children with chronic inflammatory lung disease and asthma. A prospective study was performed to evaluate the miRNA-21 and 24 levels in the EBC of patients with esophageal atresia and tracheoesophageal fistula (EA-TEF). Methods Patients operated for EA-TEF were evaluated for age, sex, type of anomaly, surgical treatment, and respiratory problems. 500–1000 μl of EBC was obtained from all patients with Ecoscreen. miRNA-21 and 24 levels in EBC were analyzed with ELISA. The results of the study group were compared with a control group (CG) consisting of healthy children with no history of respiratory problems and allergy (n = 17). miRNA levels were compared with respiratory problems and gastroesophageal reflux (GER). Results Nineteen patients with EA-TEF with a mean age of 7.8 ± 3.2 years were enrolled in the study. The male–female ratio was 10:9. The mean age of the CG was 9.1 ± 3.6 years (P > 0.05). Distal fistula (78.9%) was the most common type of anomaly. 76.5% of cases required esophageal dilatations for strictures and 15.8% of them had fistula recurrence. Fifteen of the cases with EA were diagnosed as hyperreactive airway disease and require medical treatment. When miRNA levels were compared with CG (median = 0.68), EA cases had significantly decreased levels of miRNA-21 (median = 0.64, P < 0.05). There was no difference between groups for miRNA-24 levels (P > 0.05). The miRNA levels were also compared in patients with EA, according to positive pH testing for GER, use of proton pump inhibitor (PPI) treatment, and need for fundoplication. Patients with GER in pH test (median = 0.66) and fundoplication (median = 0.66) had increased levels of miRNA-21 than patients without reflux (median = 0.63) and surgical treatment (median = 0.64) (P < 0.05). The levels of miRNA-21 and 24 did not show any significant difference in patients with and without PPI treatment (P > 0.05). Conclusion The decreased levels of miRNA-21 in EBC suggest a hyperreactive airway problem in EA patients. Increased miRNA levels in EBC are associated with GER and its surgical treatment.


2019 ◽  
Vol 132 (6) ◽  
pp. 726-730
Author(s):  
Zhu-Ping Cao ◽  
Qi-Feng Li ◽  
Shi-Qi Liu ◽  
Jian-Hua Niu ◽  
Jing-Ru Zhao ◽  
...  

2018 ◽  
Vol 53 (7) ◽  
pp. 1267-1272 ◽  
Author(s):  
Dave R. Lal ◽  
Samir K. Gadepalli ◽  
Cynthia D. Downard ◽  
Daniel J. Ostlie ◽  
Peter C. Minneci ◽  
...  

2010 ◽  
Vol 8 (1) ◽  
pp. 0-0
Author(s):  
Pranas Gurskas ◽  
Kęstutis Trainavičius ◽  
Aidas Ivanauskas ◽  
Arūnas Strumila

Pranas Gurskas, Kęstutis Trainavičius, Aidas Ivanauskas, Arūnas StrumilaVilniaus universiteto Vaikų ligų klinikos Vaikų chirurgijos centras,Santariškių g. 7, LT-2600 VilniusEl paštas: [email protected] Įvadas / tikslasPreduodeninė vartų vena (PDVV) yra labai reta įgimta anomalija. Literatūroje aprašyta per 80 atvejų. Preduodeninė vartų vena dažniausiai nesukelia jokių klinikinių simptomų. Tik nedaugeliui pacientų ji gali būti dvylikapirštės žarnos nepraeinamumo priežastis. Tyrimo tikslas – aprašyti labai retą, įgimtą dvylikapirštės žarnos obstrukcijos priežastį ir pasidalyti šios anomalijos diagnostikos ir gydymo patirtimi. Ligoniai ir metodaiMes gydėme du pacientus dėl dvylikapirštės žarnos nepraeinamumo, kurio priežastis – preduodeninė vartų vena kartu su atvirkštine skrandžio ir blužnies padėtimi, nevisiškas žarnyno posūkis. RezultataiNaujagimis ir 1 metų 4 mėnesių mergaitė buvo operuoti dėl preduodeninės vartų venos, sukėlusios dvylikapirštės žarnos obstrukciją. Abiem vaikams buvo atliktos duodenoduodenostomijos. Pooperacinė abiejų ligonių eiga buvo sklandi. Vaikai pradėjo normaliai valgyti, nustojo vemti, ėmė priaugti svorio. IšvadosDuodenoduodenostomija yra veiksminga operacija gydant dvylikapirštės žarnos obstrukciją dėl preduodeninės vartų venos. Reikšminiai žodžiai: įgimtas dvylikapirštės žarnos nepraeinamumas, preduodeninė vartų vena Congenital duodenal obstruction due to preduodenal portal vein, associated with situs inversus of stomach and spleen Pranas Gurskas, Kęstutis Trainavičius, Aidas Ivanauskas, Arūnas StrumilaVilnius University Children’s Hospital, Center of Pediatric Surgery,Santariškių Str. 7, LT-2600 Vilnius, LithuaniaE-mail: [email protected] Background / objectivePreduodenal portal vein (PDPV) is a rare congenital anomaly. There are only 80 cases described in the world literature. The presence of this anomaly is rarely recognized as an emergency condition, and it can manifest as duodenal obstruction in very few patients. The aim of our study was to descibe this uncommon reason for duodenal obstruction and to share experience in recognizing and treating this pathology. Patients and methodsAuthors present two cases of duodenal obstruction caused by the preduodenal portal vein and associated with the inverted gastric and spleen position and malrotation of the gut. ResultsA male newborn and a 1 yr 4 mon old girl were operated on due to duodenal obstruction caused by the preduodenal portal vein. Both patients received a duodenoduodenostomy procedure. The recovery was uneventful. The patients became free of symptoms, returned to oral feeds, started to thrive. ConclusionsDuodenoduodenostomy is a safe and effective procedure in treating duodenal obstruction caused by the preduodenal portalvein. Key words: duodenal obstruction, preduodenal portal vein


Author(s):  
Michał Puliński ◽  
Wojciech Choiński ◽  
Marta Stęga

Introduction: The first thoracoscopic esophageal atresia (EA) surgery in Poland was performed by Professor Dariusz Patkowski in 2005 in Wrocław. In the Clinical Ward of Pediatric Surgery and Urology, Regional Specialistic Children’s Hospital in Olsztyn, thoracoscopic EA surgery was performed on 16 January 2009. Aim: Data presentation on thoracoscopic treatment of congenital EA. Material and methods: Between 2009 and 2018 in our Clinical Ward, 28 children (11 females and 17 males) diagnosed with EA underwent treatment. All patients presented with type III EA based on the Gross classification (lower tracheoesophageal fistula and atresia of the upper segment of the trachea) and 8 of them (29.6%) were diagnosed with coexisting diseases. Results and discussion: The duration of the surgery was 70–290 minutes with a mean time of 180 minutes. Conversion was performed in 6 (21.4%) cases. Leakage of the lymph occurred in 2 (7.1%) cases . In 3 (10.7%) cases, a radiographic image showed leakage of the anastomosis. Only 1 (3.6%) patient needed reoperation due to re-canalization of tracheoesophageal fistula. Pneumothorax occurred in 2 (7.1%) cases. In total, 4 (14.3%) patients died and 23 (82.1%) patients required additional esophageal dilatation due to its narrowing. Conclusions: The treatment results of thoracoscopic EA surgeries and undeniable advantages for the patient makes this technique a highly recommended method.


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