Literature DB >> 22776303

Rectal duplication cyst successfully treated by laparoscopic total mesorectal excision using the prolapsing technique.

K Akahane1, K Uehara, Y Yoshioka, F Koide, T Ebata, Y Yokoyama, T Igami, G Sugawara, Y Takahashi, M Fukaya, K Itatsu, M Nakamura, H Goto, M Nagino.   

Abstract

Congenital alimentary tract duplication is a rare disease. It most frequently occurs in the ileum, with the rectum being the rarest site. Herein, we report a 38-year-old woman who was referred to our hospital because of severe anal pain. On digital examination, a smooth, round, rubbery mass was palpable; it was located 5 cm from the anal verge in the posterior rectal wall. A CT scan demonstrated a 5-cm cystic lesion located anterior to the sacrum that was displacing the rectum anteriorly. Spontaneous remission of the tumor was evident; however, after 5 months of follow-up, the patient experienced the same severe anal pain. MRI demonstrated a recurrent cystic lesion. To prevent further complications and to confirm or deny malignancy, laparoscopic total mesorectal excision using the prolapsing technique was performed. Pathologically, the cystic lesion was diagnosed as a rectal duplication cyst. This is the first report of a rectal duplication cyst successfully treated by laparoscopic total mesorectal excision.
© 2011 Japan Society for Endoscopic Surgery, Asia Endosurgery Task Force and Blackwell Publishing Asia Pty Ltd.

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Mesh:

Year:  2011        PMID: 22776303     DOI: 10.1111/j.1758-5910.2011.00097.x

Source DB:  PubMed          Journal:  Asian J Endosc Surg        ISSN: 1758-5902


  2 in total

Review 1.  Alimentary tract duplications in newborns and children: diagnostic aspects and the role of laparoscopic treatment.

Authors:  Jan Patiño Mayer; Marcos Bettolli
Journal:  World J Gastroenterol       Date:  2014-10-21       Impact factor: 5.742

2.  An unusual rectal duplication cyst.

Authors:  Sofia Anastasiadou; Paris Tekkis; Christos Kontovounisios
Journal:  Surg Case Rep       Date:  2019-05-09
  2 in total

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