Dergiler / İstanbul Kuzey Klinikleri / 2019 / Cilt: 6 - Sayı: 2

Congenital hiatus hernia: A case series

Sayfa
171–175
Yayın Tarihi
2022-10-18
DOI
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Yapay Zeka Hızlı Bakış & Çıkarımlar

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⚡ TL;DR(1 Cümlede Hızlı Çıkarım)

If the esophagogastric junction is present in the thorax, mediastinal dissection of the esophagus may be required to achieve a good abdominalesophagus structure, which will prevent a recurrence.

📌 3 Maddede Bu Makale

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Amaç & Hipotez:OBJECTIVE: Hiatus hernia is frequent in adults and rare in children; congenital hiatus hernia is even rarer.
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Temel Bulgular & Veri:In this study, wedescribe a group of infants with congenital hiatus hernia and discuss its management.METHODS: Records of patients (male: 3, female: 4) who were diagnosed with congenital hiatus hernia between 2010 and2016 were extracted.
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Sonuç & Katkı:If the esophagogastric junction is present in the thorax, mediastinal dissection of the esophagus may be required to achieve a good abdominalesophagus structure, which will prevent a recurrence.
🔬Tür:Araştırma Makalesi
📍Kapsam:2010 Verileri
⚙️Değişkenler:Alan Parametreleri

Abstract

OBJECTIVE: Hiatus hernia is frequent in adults and rare in children; congenital hiatus hernia is even rarer. In this study, wedescribe a group of infants with congenital hiatus hernia and discuss its management.METHODS: Records of patients (male: 3, female: 4) who were diagnosed with congenital hiatus hernia between 2010 and2016 were extracted. Demographic data, presenting symptoms, diagnostic investigations, operative details, postoperativefollow-up, and early and late postoperative complications were evaluated retrospectively.RESULTS: Four patients were female and three were male. One patient was diagnosed prenatally while the mean age atdiagnosis for others was 18.6 months. Four patients had type IV hernia, 2 had type III hernia, and one had type I hernia. Thediagnosis was confirmed by chest X-ray, computerized tomography (CT) and/or upper gastrointestinal series. The hiatal repairwas done in all patients either by laparotomy or laparoscopy. During the procedure, 2 patients had Nissen fundoplication and3 patients had Thal fundoplication. Recurrence of hernia occurred in the 2 patients who had Thal fundoplication.CONCLUSION: Recurrence of sliding hernias with Thal fundoplication seem more frequent in the series. If the esophagogastric junction is present in the thorax, mediastinal dissection of the esophagus may be required to achieve a good abdominalesophagus structure, which will prevent a recurrence.

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Bu Makaleye Atıf Yap

TUNCER, A. A., EMBLETON, D. B., ÇETİNKURŞUN, S., İLHAN, H., ARDA, M. S. (2022). Congenital hiatus hernia: A case series. İstanbul Kuzey Klinikleri, Cilt: 6 - Sayı: 2, 171–175. https://ajindex.com/articles/551488

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  1. Karpelowsky JS, Wieselthaler N, Rode H. Primary paraesophageal hernia in children. J Pediatr Surg 2006;41:1588–93. [CrossRef ] 2. Avansino JR, Lorenz ML, Hendrickson M, Jolley SG. Characterization and management of paraesophageal hernias in children after antireflux operation. J Pediatr Surg 1999;34:1610–4. [CrossRef ] 3. Imamoğlu M, Cay A, Koşucu P, Ozdemir O, Orhan F, Sapan L, et al. Congenital paraesophageal hiatal hernia: pitfalls in the diagnosis and treatment. J Pediatr Surg 2005;40:1128–33. [CrossRef ] 4. Yousef Y, Lemoine C, St-Vil D, Emil S. Congenital paraesophageal hernia: The Montreal experience. J Pediatr Surg 2015;50:1462–6. 5. Akbulut UE, Sağ E, Çakır M. Evaluation of esophageal pathology in children who underwent esophagogastroduodenoscopy. Turkish J Pediatr Dis 2017;1:9–14. [CrossRef ] 6. Kohn GP, Price RR, DeMeester SR, Zehetner J, Muensterer OJ, Awad Z, et al. Guidelines for the management of hiatal hernia. Surg Endosc 2013;27:4409–28. [CrossRef ] 7. Rai B, Ahmed R, Amer N, Sharif F. Paraesophageal hiatus hernia in an 8-month-old infant with organoaxial volvulus of the stomach. BMJ Case Rep 2014;2014. pii: bcr2014204385. [CrossRef ] 8. Ruano R, Benachi A, Aubry MC, Bernard JP, Hameury F, NihoulFekete C, et al. Prenatal sonographic diagnosis of congenital hiatal hernia. Prenat Diagn 2004;24:26–30. [CrossRef ] 9. Ogunyemi D. Serial sonographic findings in a fetus with congenital hiatal hernia. Ultrasound Obstet Gynecol 2001;17:350–3. [CrossRef ] 10. Hu JM, Hu M, Wu YM, Wang J, Yan ZL, Zhang C, et al. Long-term outcome of laparoscopic Nissen-Rossetti fundoplication versus Thal fundoplication in children with esophageal hiatal hernia: a retrospective report from two children’s medical centers in Shanghai. World J Pediatr 2016;12:231–5. [CrossRef ]