21Feb 2024

A RARE CASE OF APPENDICEAL INTUSSUSCEPTION

  • Second Year Resident, General Surgery Department, Smt. NHL Municipal Medical College.
  • Second Year Resident, General Surgery Department, Smt. NHL Municipal Medical College.
  • Third Year Resident, General Surgery Department, Smt. NHL Municipal Medical College.
  • Professor and Head of Unit, General Surgery Department, Smt. NHL Municipal Medical College.
  • Associate Professor, General Surgery Department, Smt. NHL Municipal Medical College.
  • Assistant Professor, General Surgery Department, Smt. NHL Municipal Medical College.
  • Second Year Resident, General Surgery Department, Smt. NHL Municipal Medical College.
  • Second Year Resident, General Surgery Department, Smt. NHL Municipal Medical College.
  • First Year Resident, General Surgery Department, Smt. NHL Municipal Medical College.
  • First Year Resident, General Surgery Department, Smt. NHL Municipal Medical College.
  • First Year Resident, General Surgery Department, Smt. NHL Municipal Medical College.
  • Abstract
  • Keywords
  • Cite This Article as
  • Corresponding Author

Introduction: Appendiceal intussusception is a very rare condition (0.01%) found in patients undergoing appendectomy. It happens when the appendix is pulled into itself or into the caecum. Endometriosis of the appendix is particularly a rare cause of appendiceal intussusception in the past 50 years, less than 30 cases have been reported in the literature. Clinical symptoms vary and some cases are asymptomatic.

Case Presentation: A 25 years old, female presented with complaints of periumbilical pain for 4-5 days, 6-7 episodes of bilious vomiting and constipation for 3 days. On examination, the abdomen was soft, mild tenderness was present in the periumbilical region. Patient was stable clinically. Ultrasound abdomen showed possibility of Ileo-colic Intussusception and intramural fibroid and CECT abdomen was suggestive of ileo-ileal intussusception and multiple uterine fibroids. Patient underwent Exploratory Laparotomy. Appendiceal intussusception was found in the caecum. Appendix and a part of caecum were found thickened and gangrenous. Ileocaecal junction and rest of the bowels were normal. Patient underwent ileocaecal resection with primary anastomosis.

Results: Histopathological report of specimen was consistent with findings of endometriosis of appendix with peri appendicular abscess and adenomatous changes in caecum.

Conclusion: Appendiceal intussusception to the caecum caused by endometriosis of the appendix is a very rare(0.01%) condition and difficult to diagnose preoperatively. It is usually diagnosed intra-operatively. Appendiceal intussusception due to endometriosis can only be confirmed by histopathology. 


[Nidhi Saraf, Katha Dave, Hitesh Rathva, Archana Dalal, Kalpit Suthar, Sagar Vaghela, Chintan Patel, Muhammed Viajkhora, Kinju Patel, Dev Khatri and Sunita Damor (2024); A RARE CASE OF APPENDICEAL INTUSSUSCEPTION Int. J. of Adv. Res. (Feb). 233-238] (ISSN 2320-5407). www.journalijar.com


DR NIDHI SARAF

India

DOI:


Article DOI: 10.21474/IJAR01/18287      
DOI URL: https://dx.doi.org/10.21474/IJAR01/18287