Skip to content
PubMed This is a summary of 18 peer-reviewed journal articles Updated
Gynecology

Biology & Causes: How Uterine Scarring Happens

At a Glance

Asherman syndrome occurs when the deep foundational layer of the uterine lining is damaged, usually from a surgical procedure like a D&C. This trauma triggers chronic inflammation, prompting the uterus to build tough scar tissue (adhesions) instead of healthy lining.

To understand Asherman syndrome, it helps to think of the uterine lining (endometrium) as a garden with two layers of soil. The top layer (the functionalis) is what grows and sheds every month during your period [1]. The bottom layer (the basalis) is the permanent foundation that contains the “seeds” or stem cells needed to regrow the top layer [1][2]. Asherman syndrome happens when this foundation is damaged, causing the uterus to grow scar tissue instead of healthy lining [3][4].

The Trigger: Trauma to the Foundation

Asherman syndrome is almost always caused by physical trauma to the uterine wall. When the bottom layer (the basalis) is scraped or injured, the “seeds” for regeneration are lost [3][5]. This most commonly occurs during:

  • Dilation and Curettage (D&C): A procedure to clear the uterus after a miscarriage or birth. If performed “blindly” (without a camera), there is a higher risk of accidentally scraping the basal layer [6][7]. Note: The vast majority of D&Cs heal perfectly normally and do not cause Asherman syndrome, especially when performed with ultrasound guidance.
  • Postpartum Hemorrhage Care: The uterus is particularly soft and vulnerable shortly after childbirth, making the basal layer easier to damage during medical interventions [3].
  • Uterine Surgeries: Procedures like a myomectomy (fibroid removal) can also create deep enough wounds to trigger scarring [3].

When Healing Goes Wrong

In a healthy uterus, the body repairs minor injuries by growing new, flexible tissue. In Asherman syndrome, the body switches from “repair mode” to “scar mode.” This is driven by several biological factors:

Chronic Inflammation

After an injury, the body sends “emergency” immune cells to the area. In Asherman syndrome, these cells stay too long and release constant distress signals [8][9]. This constant state of alarm tells the body to keep building tough, fibrous tissue rather than soft, healthy lining [9].

A Cellular Identity Crisis

One of the most complex parts of this process is a cellular identity crisis where normal cells forget their purpose [10].

  • Normally, the cells lining your uterine blood vessels have a specific job: helping blood flow and nutrients reach the lining.
  • In response to severe trauma and inflammation, these cells lose their identity [11][12].
  • They transform into myofibroblasts—cells that act like construction workers whose only job is to pump out collagen, the main ingredient in scar tissue [13][14].

From Lining to Adhesions

As these myofibroblasts take over, they fill the uterine cavity with tough, non-functional fibers. Because the uterus is a flat, muscular organ, these scars often act like glue, causing the front and back walls of the uterus to stick together (adhesions) [15][16]. Once this bridge of scar tissue forms, the healthy lining can no longer grow over it, leading to the symptoms of light or absent periods [4][16].

Modern research is currently focused on how to “reset” this environment—using stem cell therapies or growth factors to convince the uterus to stop making scars and start regrowing the foundation [17][18].

Common questions in this guide

What causes Asherman syndrome?
Asherman syndrome is almost always caused by physical trauma to the deep layer of the uterine wall. This usually happens during procedures like a D&C, fibroid removal, or treatment for postpartum bleeding, which can damage the cells needed to regrow the uterine lining.
Why does a D&C sometimes cause uterine scarring?
If a D&C is performed without a camera or ultrasound guidance, there is a risk of accidentally scraping the deep basal layer of the uterus. When this foundation is damaged, the body may heal by forming scar tissue instead of regrowing a healthy lining.
How does inflammation lead to intrauterine adhesions?
After a uterine injury, chronic inflammation can cause immune cells to stay in the area too long. This constant state of alarm triggers cells to produce tough, fibrous collagen, creating scar tissue that glues the front and back walls of the uterus together.
Can my uterine lining regrow if I have Asherman syndrome?
Regrowing the lining depends on how much of your foundational layer remains intact. Doctors often use a combination of scar removal, barrier gels like hyaluronic acid to prevent new scars, and estrogen protocols to encourage your healthy lining to regrow.

Questions to Ask Your Doctor

Curated prompts to bring to your next appointment.

  1. 1.How much of my basal layer remains intact according to my ultrasound or hysteroscopy results?
  2. 2.Would you recommend using hyaluronic acid gel or other barrier agents to prevent further fibrosis after my procedure?
  3. 3.Do you suspect that chronic inflammation or an undetected infection played a role in my scarring?
  4. 4.What is your protocol for using estrogen to help my healthy lining (the functionalis layer) regrow?

Questions For You

Tap a prompt to share your answer — we'll use it plus this page's context to start a tailored conversation.

References

References (18)
  1. 1

    Expression of ALDH1A Isozymes in Human Endometrium with and without Endometriosis and in Ovarian Endometrioma.

    Ma S, Hirata T, Arakawa T, et al.

    Reproductive sciences (Thousand Oaks, Calif.) 2020; (27(1)):443-452 doi:10.1007/s43032-019-00041-4.

    PMID: 32046407
  2. 2

    N-cadherin identifies human endometrial epithelial progenitor cells by in vitro stem cell assays.

    Nguyen HPT, Xiao L, Deane JA, et al.

    Human reproduction (Oxford, England) 2017; (32(11)):2254-2268 doi:10.1093/humrep/dex289.

    PMID: 29040564
  3. 3

    Mini-Review of the New Therapeutic Possibilities in Asherman Syndrome-Where Are We after One Hundred and Twenty-Six Years?

    Doroftei B, Dabuleanu AM, Ilie OD, et al.

    Diagnostics (Basel, Switzerland) 2020; (10(9)) doi:10.3390/diagnostics10090706.

    PMID: 32957624
  4. 4

    Uterine stem cells: from basic research to advanced cell therapies.

    Santamaria X, Mas A, Cervelló I, et al.

    Human reproduction update 2018; (24(6)):673-693 doi:10.1093/humupd/dmy028.

    PMID: 30239705
  5. 5

    Clinical features of the predilection and severer sites of intrauterine adhesions.

    Yu Y, Zou L, Li W, et al.

    Zhong nan da xue xue bao. Yi xue ban = Journal of Central South University. Medical sciences 2022; (47(11)):1568-1574 doi:10.11817/j.issn.1672-7347.2022.220248.

    PMID: 36481635
  6. 6

    Identifying the risk factors and incidence of Asherman Syndrome in women with post-abortion uterine curettage.

    Sevinç F, Oskovi-Kaplan ZA, Çelen Ş, et al.

    The journal of obstetrics and gynaecology research 2021; (47(4)):1549-1555 doi:10.1111/jog.14667.

    PMID: 33462894
  7. 7

    Incidence and Risk Factors for Intrauterine Synechiae in Women With Previous Dilation and Curettage.

    Chen S, Samiezade-Yazd Z, Triplett C, Joshi N

    Obstetrics and gynecology 2026; (147(3)):366-373 doi:10.1097/AOG.0000000000006158.

    PMID: 41505760
  8. 8

    The predictive value of serum IL-17A and IL-6 expression in postoperative recurrence in patients with intrauterine adhesion.

    Cui X, Xiao HC, Pan W

    American journal of reproductive immunology (New York, N.Y. : 1989) 2024; (91(1)):e13808 doi:10.1111/aji.13808.

    PMID: 38282600
  9. 9

    Single-cell sequencing uncovers disrupted stromal-macrophage communication as a driver of intrauterine adhesion progression.

    Dong E, Zhou Z, Chen T, et al.

    Communications biology 2025; (8(1)):1194 doi:10.1038/s42003-025-08634-3.

    PMID: 40790346
  10. 10

    XBP1 promotes endometrial fibrosis through cGAS-STING signaling pathway in intrauterine adhesion.

    Wu X, He L, Lin Y, et al.

    Scientific reports 2025; (15(1)):23299 doi:10.1038/s41598-025-06162-y.

    PMID: 40603996
  11. 11

    Linking EMT programmes to normal and neoplastic epithelial stem cells.

    Lambert AW, Weinberg RA

    Nature reviews. Cancer 2021; (21(5)):325-338 doi:10.1038/s41568-021-00332-6.

    PMID: 33547455
  12. 12

    Reduced expression of SMAD7 and consequent reduction of autophagy promotes endometrial stromal-myofibroblast transition and fibrosis.

    Yong M, Zhou H, Zeng Y, et al.

    Molecular human reproduction 2024; (30(10)) doi:10.1093/molehr/gaae036.

    PMID: 39412480
  13. 13

    Endothelium-mediated contributions to fibrosis.

    Sun X, Nkennor B, Mastikhina O, et al.

    Seminars in cell & developmental biology 2020; (101()):78-86 doi:10.1016/j.semcdb.2019.10.015.

    PMID: 31791693
  14. 14

    Role of epithelial-mesenchymal transition in proliferative vitreoretinopathy.

    Tamiya S, Kaplan HJ

    Experimental eye research 2016; (142()):26-31.

    PMID: 26675400
  15. 15

    MicroRNA-29b Inhibits Endometrial Fibrosis by Regulating the Sp1-TGF-β1/Smad-CTGF Axis in a Rat Model.

    Li J, Du S, Sheng X, et al.

    Reproductive sciences (Thousand Oaks, Calif.) 2016; (23(3)):386-94 doi:10.1177/1933719115602768.

    PMID: 26392347
  16. 16

    Secondary Prevention of Intrauterine Adhesions Following Hysteroscopic Surgery in Women With Asherman Syndrome: Is Something Better Than Nothing?

    Kelley AS, Giuliani E, Schon SB

    Clinical obstetrics and gynecology 2020; (63(2)):320-326 doi:10.1097/GRF.0000000000000510.

    PMID: 31815774
  17. 17

    Adipose derived mesenchymal stem cell treatment in experimental asherman syndrome induced rats.

    Çil N, Yaka M, Ünal MS, et al.

    Molecular biology reports 2020; (47(6)):4541-4552 doi:10.1007/s11033-020-05505-4.

    PMID: 32444974
  18. 18

    hUMSCs Restore Uterine Function by Inhibiting Endometrial Fibrosis via Regulation of the MMP-9/TIMP-1 Ratio in CDDP-Induced Injury Rats.

    Tang Y, Si Y, Liu C, et al.

    Stem cells international 2023; (2023()):8014052 doi:10.1155/2023/8014052.

    PMID: 36994440

This information explains the biology and causes of Asherman syndrome for educational purposes only. Always consult your gynecologist or reproductive specialist regarding your specific symptoms or surgical history.

Get notified when new evidence is published on Asherman syndrome.

We monitor PubMed for new peer-reviewed studies on this topic and email a short summary when something meaningful changes.