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Kolestazın nadir bir nedeni: Konjenital sağ diafragma hernisi

Yıl 2020, Cilt: 4 Sayı: 11, 1089 - 1091, 01.11.2020
https://doi.org/10.28982/josam.731192

Öz

82 günlük kız hasta ani gelişen sarılık, akolik dışkılama olması nedeniyle yapılan Abdominal Ultrasonografisinde safra kesesinin görülmemesi üzerine kliniğimize yönlendirildi. Akciğer grafisinde sağ diyafram elevasyonu mevcut idi. Hastanın muayenesinde aynı tarafta solunum sesleri azalmış olarak alınıyor idi. Çekilen Tomografisinde sağ diyafragmatik herni mevcut ve karaciğer ile safra kesesi toraks boşluğuna herniye idi. Olgumuzda sağ Bochdalek hernisi mevcut idi ve safrayollarının torasik kavitede sıkışmasına bağlı obstrüktif sarılık gelişmiş idi. Operasyon sırasında alınan karaciğer biyopsisinde fibroz bulguları oluşmaya başlamış idi. Operasyona alınan hastanın abdominal organları yerine alınarak, kolesistektomi ve hepatikojejunostomi operasyonu yapıldı. Erken tanı ve tedavi ile hastanın takibinde yapılan karaciğer biyopsisinde karaciğerde gelişen bulguların düzelmeye başladığı görüldü. Kolestaz, çok çeşitli etyolojik nedenlere bağlı olabilmekle birlikte cerrahi nedenlerin ivedilikle tanı ve tedavisinin yapılması prognoz açısıdan önem arz etmektedir. Bu olgu ile Bochdalek hernisinin çok farklı bir prezantasyon şeklini sunmak istedik. Kolestaz ile gelen akolik dışkısı mevcut olan hastaların ayırıcı tanısında diafragma hernisi de akılda tutulmalıdır.

Kaynakça

  • 1. Jain V, Agarwala S, and Bhatnagar V. Recent advances in the management of congenital diaphragmatic hernia. Indian Journal of Pediatrics. 2010;77(6):673–8.
  • 2. Migliazza L, Bellan C, Alberti D, Auriemma A, Burgio G, Locatelli G, et al. Retrospective study of 111 cases of congenital diaphragmatic hernia treated with early high-frequency oscillatory ventilation and presurgical stabilization. J Pediatr Surg. 2007;42:1526–32.
  • 3. Kinoshita F, Ishiyama M, Honda S, Matsuzako M, Oikado K, Kinoshita T, et al. Late-presenting posterior transdiaphragmatic (Bochdalek) hernia in adults: prevalence and MDCT characteristics. Journal of Thoracic Imaging. 2009;24(1):17–22.
  • 4. Jones HG, Kadhim A, Nutt M. Congenital diaphragmatic hernia: an unusual cause of obstructive jaundice. Ann R Coll Surg Engl. 2012;94:8-9.
  • 5. Sandstrom CK, Stern EJ. “Diaphragmatic hernias: a spectrum of radiographic appearances,” Current Problems in Diagnostic Radiology 2011;40(3):95–115.
  • 6. Becmeur F, Jamali RR, Moog R, Keller L, Christmann D, Donato L, et al. Thoracoscopic treatment for delayed presentation of congenital diaphragmatic hernia in the infant: A report of three cases. Surg Endosc. 2001;15:1163-6.
  • 7. Bagłaj M. Late-presenting congenital diaphragmatic hernia in children: a clinical spectrum. Pediatr Surg Int. 2004;20:658-69.
  • 8. Coco D, Leanza S. An Atypical Presentation of a Strangulated Bochdalek Hernia in a 60-Year-Old Man. Macedonian Journal of Medical Sciences. 2019;7(11):1818-20.
  • 9. Lewis DA, Reickert C, Bowerman R, Hirschl RB. Prenatal ultrasonography frequently fails to diagnose congenital diaphragmatic hernia. J Pediatr Surg. 1997;32:352-6.
  • 10. Garne E, Haeusler M, Barisic I, Gjergja R, Stoll C, Clementi M. Congenital diaphragmatic hernia: Evaluation of prenatal diagnosis in 20 European regions. Ultrasound Obstet Gynecol. 2002;19:329-33.
  • 11. Zeina AR, Weiner D, Reindorp N, Kassem E, Klein-Kremer A. Late presentation of congenital right diaphragmatic hernia: clinical and radiological features. Pediatr Int. 2011;53:790-1.
  • 12. Sutedja B and Muliani Y. Laparoscopic repair of a Bochdalek hernia in an adult woman . Asian J Endosc Surg. 2015;8:354-6.

A rare cause of cholestasis: Congenital right diaphragmatic hernia

Yıl 2020, Cilt: 4 Sayı: 11, 1089 - 1091, 01.11.2020
https://doi.org/10.28982/josam.731192

Öz

An 82-day-old infant, investigated for sudden onset jaundice and acholic feces, was referred to our department, as no gallbladder was observed by abdominal ultrasonography. Her chest x-ray revealed an elevated right diaphragm, and the breath sounds were diminished on the right. Suspicious arteriovenous malformation in the fifth segment of the right lobe accompanied by a rotation anomaly of liver was reported. Tomography scans showed right diaphragmatic hernia where the left lobe of liver and gallbladder herniated to the thoracic space. In this case with right Bochdalek hernia, the bile ducts had kinked in the thoracic cavity, causing obstructive jaundice. If the kinking continues despite relocation of organs into the abdominal cavity, cholecystectomy-hepaticojejunostomy is an effective and reliable surgical method. Myriad pathologies may cause cholestasis, and surgical reasons should be investigated and diagnosed without delay to improve prognosis. For closure of the diaphragmatic defect, primary repair should be the preferred method. With this case, we wanted to emphasize a highly different presentation of Bochdalek hernia and remind that diaphragmatic hernia should be kept in mind in patients presenting with cholestasis and acholic stools.

Kaynakça

  • 1. Jain V, Agarwala S, and Bhatnagar V. Recent advances in the management of congenital diaphragmatic hernia. Indian Journal of Pediatrics. 2010;77(6):673–8.
  • 2. Migliazza L, Bellan C, Alberti D, Auriemma A, Burgio G, Locatelli G, et al. Retrospective study of 111 cases of congenital diaphragmatic hernia treated with early high-frequency oscillatory ventilation and presurgical stabilization. J Pediatr Surg. 2007;42:1526–32.
  • 3. Kinoshita F, Ishiyama M, Honda S, Matsuzako M, Oikado K, Kinoshita T, et al. Late-presenting posterior transdiaphragmatic (Bochdalek) hernia in adults: prevalence and MDCT characteristics. Journal of Thoracic Imaging. 2009;24(1):17–22.
  • 4. Jones HG, Kadhim A, Nutt M. Congenital diaphragmatic hernia: an unusual cause of obstructive jaundice. Ann R Coll Surg Engl. 2012;94:8-9.
  • 5. Sandstrom CK, Stern EJ. “Diaphragmatic hernias: a spectrum of radiographic appearances,” Current Problems in Diagnostic Radiology 2011;40(3):95–115.
  • 6. Becmeur F, Jamali RR, Moog R, Keller L, Christmann D, Donato L, et al. Thoracoscopic treatment for delayed presentation of congenital diaphragmatic hernia in the infant: A report of three cases. Surg Endosc. 2001;15:1163-6.
  • 7. Bagłaj M. Late-presenting congenital diaphragmatic hernia in children: a clinical spectrum. Pediatr Surg Int. 2004;20:658-69.
  • 8. Coco D, Leanza S. An Atypical Presentation of a Strangulated Bochdalek Hernia in a 60-Year-Old Man. Macedonian Journal of Medical Sciences. 2019;7(11):1818-20.
  • 9. Lewis DA, Reickert C, Bowerman R, Hirschl RB. Prenatal ultrasonography frequently fails to diagnose congenital diaphragmatic hernia. J Pediatr Surg. 1997;32:352-6.
  • 10. Garne E, Haeusler M, Barisic I, Gjergja R, Stoll C, Clementi M. Congenital diaphragmatic hernia: Evaluation of prenatal diagnosis in 20 European regions. Ultrasound Obstet Gynecol. 2002;19:329-33.
  • 11. Zeina AR, Weiner D, Reindorp N, Kassem E, Klein-Kremer A. Late presentation of congenital right diaphragmatic hernia: clinical and radiological features. Pediatr Int. 2011;53:790-1.
  • 12. Sutedja B and Muliani Y. Laparoscopic repair of a Bochdalek hernia in an adult woman . Asian J Endosc Surg. 2015;8:354-6.
Toplam 12 adet kaynakça vardır.

Ayrıntılar

Birincil Dil İngilizce
Konular Gastroenteroloji ve Hepatoloji
Bölüm Olgu sunumu
Yazarlar

Didem Gülcü Taşkın 0000-0002-2746-3799

Şenol Emre 0000-0001-9526-7151

Evrim Özmen 0000-0003-3100-4197

Nuray Kepil 0000-0001-5494-6422

İbrahim Adaletli 0000-0003-4531-6466

Tufan Kutlu Bu kişi benim 0000-0001-8396-4048

Fugen Cullu Bu kişi benim 0000-0003-0886-1422

Tulay Erkan 0000-0002-8924-2799

Osman Senyuz Bu kişi benim 0000-0002-0652-5524

Yayımlanma Tarihi 1 Kasım 2020
Yayımlandığı Sayı Yıl 2020 Cilt: 4 Sayı: 11

Kaynak Göster

APA Gülcü Taşkın, D., Emre, Ş., Özmen, E., Kepil, N., vd. (2020). A rare cause of cholestasis: Congenital right diaphragmatic hernia. Journal of Surgery and Medicine, 4(11), 1089-1091. https://doi.org/10.28982/josam.731192
AMA Gülcü Taşkın D, Emre Ş, Özmen E, Kepil N, Adaletli İ, Kutlu T, Cullu F, Erkan T, Senyuz O. A rare cause of cholestasis: Congenital right diaphragmatic hernia. J Surg Med. Kasım 2020;4(11):1089-1091. doi:10.28982/josam.731192
Chicago Gülcü Taşkın, Didem, Şenol Emre, Evrim Özmen, Nuray Kepil, İbrahim Adaletli, Tufan Kutlu, Fugen Cullu, Tulay Erkan, ve Osman Senyuz. “A Rare Cause of Cholestasis: Congenital Right Diaphragmatic Hernia”. Journal of Surgery and Medicine 4, sy. 11 (Kasım 2020): 1089-91. https://doi.org/10.28982/josam.731192.
EndNote Gülcü Taşkın D, Emre Ş, Özmen E, Kepil N, Adaletli İ, Kutlu T, Cullu F, Erkan T, Senyuz O (01 Kasım 2020) A rare cause of cholestasis: Congenital right diaphragmatic hernia. Journal of Surgery and Medicine 4 11 1089–1091.
IEEE D. Gülcü Taşkın, “A rare cause of cholestasis: Congenital right diaphragmatic hernia”, J Surg Med, c. 4, sy. 11, ss. 1089–1091, 2020, doi: 10.28982/josam.731192.
ISNAD Gülcü Taşkın, Didem vd. “A Rare Cause of Cholestasis: Congenital Right Diaphragmatic Hernia”. Journal of Surgery and Medicine 4/11 (Kasım 2020), 1089-1091. https://doi.org/10.28982/josam.731192.
JAMA Gülcü Taşkın D, Emre Ş, Özmen E, Kepil N, Adaletli İ, Kutlu T, Cullu F, Erkan T, Senyuz O. A rare cause of cholestasis: Congenital right diaphragmatic hernia. J Surg Med. 2020;4:1089–1091.
MLA Gülcü Taşkın, Didem vd. “A Rare Cause of Cholestasis: Congenital Right Diaphragmatic Hernia”. Journal of Surgery and Medicine, c. 4, sy. 11, 2020, ss. 1089-91, doi:10.28982/josam.731192.
Vancouver Gülcü Taşkın D, Emre Ş, Özmen E, Kepil N, Adaletli İ, Kutlu T, Cullu F, Erkan T, Senyuz O. A rare cause of cholestasis: Congenital right diaphragmatic hernia. J Surg Med. 2020;4(11):1089-91.