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Asherman syndrome, also known as Asherman’s syndrome or intrauterine adhesions, is a rare genetic condition in which scar tissue develops in your uterine cavity and affects your menstrual cycles. The scar tissue commonly runs from one wall of the uterus to the other but also can be flat in some instances, and it can replace the normal lining of the uterus.
Our team of providers offers you compassionate, expert care in which we properly screen for the condition and offer effective treatments to break up scar tissue and prevent it from growing back.
In some cases, you may not experience symptoms. But common symptoms include:
Most women with Asherman syndrome develop it after having surgery that involves their uterus, such as a dilation, which removes part of the lining of the uterus to treat heavy periods or clear the lining of the uterus after an abortion or miscarriage. The buildup of scar tissue also can be related to an infection of the uterus following an abortion, miscarriage, or delivery.
Although uncommon, you could develop Asherman syndrome without having any of these common factors.
A hysteroscopy, a technique that doctors use to look directly in your uterus to identify scar tissue, is the most effective way to diagnose Asherman syndrome. Depending on the severity and type of scar tissue, it also may be possible to break up some of the scar tissue at the time of initial diagnosis.
Additional tests that may be performed include:
An HSG and sonohysterogram can suggest the presence of Asherman syndrome, but they don’t provide doctors with the level of visualization that hysteroscopies do. Transvaginal ultrasounds, meanwhile, can evaluate and measure the thickness of the endometrial lining.
We use guidelines from the American Society for Reproductive Medicine to classify the three different stages of Asherman syndrome, which include:
If you have Asherman syndrome, but you don’t have any symptoms and aren’t interested in having children, there is no medical reason why your scar tissue needs to be treated. If you do want or need treatment, however, treating Asherman syndrome involves two primary steps.
The first step of treatment is breaking up scar tissue, opening the uterine cavity, and identifying the tubal ostia (the openings of the fallopian tubes into the uterus).
If the scar tissue is thin and filmy, it can be broken up bluntly using the hysteroscope. If the adhesions are thick and dense, your surgeon will use scissors to cut the scar tissue. The goal of the surgery is to completely open up the uterine cavity and be able to identify both tubal ostia. We sometimes use ultrasound to help guide the break down of adhesions.
Your doctor will perform your surgery in the office or operating room, depending on your circumstances and the extent of your adhesions. Most women go home the same day of surgery, have quick recoveries, and need minimal pain medication after surgery.
A challenge with Asherman syndrome is keeping scar tissue away once it’s removed. While several techniques exist to prevent scar tissue from coming back, none have been shown to work better than another. These techniques include:
Connect with our team to discuss your Asherman syndrome care options.