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Endoscopically monitored canalization for treatment of congenital cervical atresia: the least invasive approach.

Research Authors
El Saman AM1.
Research Journal
Fertil Steril. 2010 Jun;94(1):313-6. doi: 10.1016/j.fertnstert.2009.02.079. Epub 2009 May 21
Research Member
Research Publisher
Fertil Steril. 2010 Jun;94(1):313-6. doi: 10.1016/j.fertnstert.2009.02.079. Epub 2009 May 21
Research Rank
1
Research Vol
Fertil Steril. 2010 Jun;94(1):313-6. doi: 10.1016/j.fertnstert.2009.02.079. Epub 2009 May 21
Research Website
PMID: 17572428 [PubMed - indexed for MEDLINE
Research Year
2010
Research_Pages
NULL
Research Abstract

Abstract
OBJECTIVE:

To study feasibility, safety, and anatomic and functional outcomes of endoscopically monitored canalization for treatment of congenital cervical atresia.
DESIGN:

Case series with description of the technique.
SETTING:

Assiut University Women's Health Center.
PATIENT(S):

Five with congenital cervical atresia, two of them with associated vaginal aplasia.
INTERVENTION(S):

The three cases with isolated cervical atresia underwent laparoscopic canalization under vaginoscopic monitoring (LC-VM). The two cases with associated vaginal aplasia underwent laparoscopic canalization under tactile monitoring (LC-TM). Cystoscopy was done for all cases to ensure bladder and urethral integrity.
MAIN OUTCOME MEASURE(S):

Operative time, complication rate, menstrual pattern, and reintervention rate.
RESULT(S):

The LC-VM procedure was performed successfully in three cases within 20-25 minutes. The two cases with associated vaginal aplasia underwent LC-TM; one them was successful and the other was complicated with bladder puncture. Follow-up ranged from 3 to 36 months, and all had regular menstruation.
CONCLUSION(S):

Laparoscopic canalization under vaginoscopic monitoring is a simple, effective, and minimally invasive way of management of isolated cervical atresia. However it seems not to be the ideal technique and needs further refinements for treatment of cervical atresia associated with vaginal aplasia.