A rare case of Bochdalek diaphragmatic hernia with concomitant partial situs inversus

Authors

  • Rishabh Jain Department of Surgery, Dr. D Y Patil College of Medicine, Nerul, Navi Mumbai, Maharashtra
  • Ajay Gujar Department of Surgery, Dr. D Y Patil College of Medicine, Nerul, Navi Mumbai, Maharashtra
  • Naseem Khan Department of Surgery, Dr. D Y Patil College of Medicine, Nerul, Navi Mumbai, Maharashtra
  • Lokesh Sreedharan Department of Surgery, Dr. D Y Patil College of Medicine, Nerul, Navi Mumbai, Maharashtra
  • Tanveer Parvez Shaikh Department of Surgery, Dr. D Y Patil College of Medicine, Nerul, Navi Mumbai, Maharashtra
  • Roshan Palresha Department of Emergency Medicine, Dr. D Y Patil College of Medicine, Nerul, Navi Mumbai, Maharashtra
  • Chaitanya Burra Department of Surgery, Dr. D Y Patil College of Medicine, Nerul, Navi Mumbai, Maharashtra

Keywords:

Congenital diaphragmatic hernias, Bochdalek hernia, Morgagni hernia

Abstract

Congenital diaphragmatic hernias clinically presenting in adulthood are exceedingly rare lesions, mainly left-sided defect (Bochdalek). Bochdalek hernias most commonly manifest during the patient’s first few weeks of life. Diagnosis beyond the first 8 weeks of life is estimated to represent 5-25% of all Bochdalek hernias. Here we have a 32 year old female patient who presented with 10x10 cm diaphragmatic hernia with dextrocardia who was asymptomatic for years.

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References

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Published

2017-01-05

How to Cite

Jain, R., Gujar, A., Khan, N., Sreedharan, L., Shaikh, T. P., Palresha, R., & Burra, C. (2017). A rare case of Bochdalek diaphragmatic hernia with concomitant partial situs inversus. International Journal of Research in Medical Sciences, 3(2), 494–497. Retrieved from https://www.msjonline.org/index.php/ijrms/article/view/1307

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Section

Case Reports