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Do You Need Two Ultrasounds Before Bowel Endometriosis Surgery?

Mapping rectal endometriosis with TVS and ERUS to tailor surgery and expectations

By Dr Steven Vasilev
A female clinician reviews side-by-side TVS and ERUS ultrasound images with a female patient in a bright exam room to illustrate mapping before bowel endometriosis surgery.

When rectal endometriosis is suspected, “mapping” changes everything


If you’re living with bowel symptoms—pain with bowel movements, constipation/diarrhea flares around your period, deep pelvic pain, painful sex, bloating, or that frightening feeling of “something is stuck”—it can be validating (and overwhelming) to hear the words rectal endometriosis or bowel deep endometriosis.


One of the biggest practical challenges is that bowel endometriosis isn’t just “present or not.” What matters for your treatment plan is where it is, how big it is, and how deep it goes into the bowel wall—because that can change the kind of surgery recommended, the surgeon you need on the team, and your risk of bowel complications.


Recent evidence supports a very patient-relevant idea: using two different ultrasound approaches before surgery can give a fuller picture than using only one—especially when the goal is planning the safest, least aggressive surgery that still treats your symptoms.


The two ultrasound tests you may hear about


Transvaginal ultrasound (TVS)


This is the pelvic ultrasound done with a vaginal probe (often similar to scans used in fertility workups). Many endometriosis-experienced sonographers can “map” deep endometriosis with TVS—looking at ovaries, uterosacral ligaments, pouch of Douglas, and signs that bowel may be involved.


Real-world plus: It’s widely available and can assess pelvic organs beyond the bowel.

Common limitation: TVS may not reliably show all rectal nodules or clearly define which bowel wall layers are involved.


Endorectal ultrasound (ERUS)


ERUS uses a probe in the rectum to visualize the rectal wall in layers. If you’ve been told, “We need to know whether this goes into the muscular layer or deeper,” ERUS is one tool that aims to answer that.


Real-world plus: It can give detailed information about depth of invasion in the rectal wall.

Common limitation: It may sometimes overestimate how deep disease goes (which matters because “deeper” can push surgeons toward more extensive procedures).


What “two ultrasounds” can add for you


In a small prospective cohort where patients had both TVS and ERUS before surgery for rectal endometriosis, TVS identified rectal nodules in about 60.9% of patients, while ERUS characterized nodules in all included patients. In other words: if TVS doesn’t clearly show a rectal nodule but your symptoms and exam strongly suggest bowel involvement, ERUS (in the right hands) may provide additional detail.


The more important patient-facing point isn’t “which test is best” in the abstract—it’s this:


Better pre-op mapping can help your team plan a surgery that fits your anatomy, including whether bowel surgery is likely and what type. It can also help you prepare emotionally and practically (time off work, recovery expectations, the right surgical specialists in the room).


Why depth and “layers” matter (and why ERUS can be helpful)


Your rectum has layers. Endometriosis might affect:

  • the outer surface,
  • the muscular layer (common in deep disease),
  • and rarely the submucosa/mucosa (deeper layers closer to the inside).


In this cohort, ERUS was reported to have 100% sensitivity for detecting mucosa/submucosa involvement (meaning it caught all cases that truly had it), but 73.9% specificity (meaning it sometimes suggested mucosal/submucosal involvement when surgery/pathology didn’t confirm it). For you, that translates to:

  • ERUS can be useful for not “missing” deep involvement.
  • But if ERUS suggests very deep invasion, it’s worth asking how your team confirms that finding and how strongly it will influence the surgical plan. If the team includes surgeons who are used to performing resections and stapled anastomosis (with or without a colostomy being required, which is usually temporary but lifestyle altering), then you may not get consideration of a lesser resection like a disc or even shaving attempt first.


How imaging can influence the type of bowel surgery offered


If bowel endometriosis is confirmed and you’re considering surgery, there are several surgical approaches. The goal is symptom relief while minimizing risk.


In this cohort, surgeons most often used:

  • Rectal shaving: 52.2% (12/23)
  • Disc excision: 34.8% (8/23)
  • Segmental resection: 13.0% (3/23)


Here’s what those terms generally mean in patient language:


Shaving: Removing endometriosis from the surface of the bowel (and sometimes into superficial muscle) without cutting out a full thickness segment. Often considered “less aggressive.”


Disc excision: Removing a “disc” of bowel wall where the nodule is (full-thickness at that spot) and closing the bowel.


Segmental resection: Removing a segment of bowel and rejoining the ends. This is usually considered when disease is extensive, involves multiple areas, causes narrowing, or deeply infiltrates in a way that shaving/disc excision may not be safe or effective.


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A key practical detail: narrowing (stenosis) showed up with segmental resections


In this cohort, luminal stenosis (narrowing) was seen in 2 out of 3 people who had segmental resection (66.7%)—and those patients also had larger nodules on ERUS measurements.


You shouldn’t take that as “segmental resection causes stenosis” (the numbers are tiny and people getting resections are often the most severe cases). But you can take this to your appointment as a real-life planning point:


If imaging suggests a larger lesion or significant narrowing, your surgeon may recommend segmental resection—and you deserve a clear explanation of why, what alternatives exist, and what the functional risks are (bowel habit changes, urgency, constipation, leaks, etc.). In some cases, it may be prudent to have a gastroenterologist perform a colonoscopy to confirm what they see and to "ink" areas that look like they are involved very deeply or even into the lumen (the inside) of the bowel.


What you might feel better after surgery—and what might not change quickly


At 3 months after surgery in this cohort, multiple endometriosis quality-of-life areas improved significantly, including:

  • Pain
  • Emotional well-being
  • Work-related functioning
  • Sexual relationship concerns


That matches many patients’ lived experiences: pain relief can be meaningful, and the mental load can lift when symptoms are treated.


But digestive quality-of-life (measured by a GI quality-of-life tool) improved only numerically and was not statistically significant at 3 months. A very practical takeaway is:


Your bowel function may take longer to settle than your pelvic pain.

It’s also possible that some bowel symptoms come from overlapping issues (IBS, pelvic floor dysfunction, dietary triggers, nerve sensitization) even when endometriosis is treated well.


If bowel symptoms are your main complaint, talk with your team about a recovery timeline that includes pelvic floor rehab, diet support, and realistic expectations for the first 3–6 months.


Safety: what complications looked like here


In this cohort, there were:

  • No Grade III or IV complications reported
  • One Grade II complication (rectal bleeding)


This is reassuring, but it’s still crucial to personalize risk. Complication rates depend heavily on:

  • surgeon and center experience,
  • extent of disease,
  • whether resection is needed,
  • whether you also have bladder/ureter involvement,
  • and your baseline bowel function.


Who might benefit most from adding ERUS to TVS?


You might consider asking about ERUS (in addition to TVS) if:

  • your symptoms strongly suggest bowel involvement but TVS is unclear,
  • your TVS shows a rectal nodule and your surgeon needs more detail on depth,
  • there’s concern for bowel narrowing/stenosis,
  • or you’re trying to avoid an overly aggressive bowel surgery and want the best possible mapping.


ERUS is not available everywhere and is operator-dependent. In some centers, MRI may be used instead of or alongside ERUS/TVS. What matters is not the “perfect test,” but getting high-quality imaging interpreted by people who routinely map deep endometriosis.


Questions to ask your doctor (bring these to your pre-op visit)

  • “Based on my symptoms and exam, do you suspect rectal endometriosis—and what imaging best maps it in your practice?”
  • “Would TVS plus ERUS add information in my case, or would MRI be more useful?”
  • “If ERUS suggests deep layers are involved, how do you confirm that—and how will it change the surgical plan?”
  • “Given my imaging, what’s the most likely procedure: shaving, disc excision, or segmental resection—and what would make you switch plans during surgery?”
  • “Will a colorectal surgeon or a gynecologic oncologist be present? If not, under what circumstances would you involve one?”
  • “What bowel function changes are most common after the type of surgery you’re recommending, and what support do you offer (pelvic floor PT, dietitian, follow-up plan)?”


Reality check: what this doesn’t settle (and why your plan must be individualized)


Even though dual ultrasound mapping is promising, there are still major unknowns:

  • This evidence comes from a small cohort, and imaging performance numbers (like sensitivity/specificity for deep layers) are based on very few cases.
  • Follow-up was short (3 months), so it doesn’t answer long-term questions like recurrence, long-term bowel function, or fertility outcomes.
  • Imaging quality varies hugely by operator and equipment; a “normal” scan does not always equal “no disease.”


Your best next step is to use imaging as a tool for shared decision-making: balancing symptom severity, your fertility goals, your tolerance for risk, and the experience level of the surgical team.

References

  1. Yan H, Zhang G, Zhong G, et al. Dual ultrasound combination improves the accuracy of preoperative assessment in rectal endometriosis: a prospective cohort study. Annals of Medicine and Surgery. 2025. DOI: 10.1097/MS9.0000000000004293

Quick Answers

What should I tell ER staff about my endometriosis?

If you’re in the ER with pelvic or abdominal pain and you have endometriosis (or strong suspicion of it), lead with the facts that help them triage safely: your diagnosis status (surgically confirmed vs suspected), any prior operative and pathology findings, and whether you’ve had complications like bowel, bladder, appendix, or diaphragm/thoracic involvement. Tell them what today’s pain is doing differently from your baseline—sudden onset, one-sided or right-lower-quadrant pain, fever, vomiting, fainting, heavy bleeding, chest/shoulder pain, or shortness of breath—and whether it seems cyclical or tied to your period. ER teams are trained to rule out emergencies first, so describing “what changed” and “what worries you most” helps them move faster and document the right differentials.


It also helps to be very specific about your symptom pattern and functional impact rather than just saying “endo flare.” For example: pain with urination or bladder filling, pain with bowel movements, constipation/diarrhea flares, rectal pressure, deep pain with sex, or pain that radiates to the back/leg—especially if those symptoms have a clear cycle pattern. If you have records, bring or show the most useful ones: operative reports, pathology reports, and recent imaging reports (and images if you have them). Those details can prevent your history from being minimized just because a CT or ultrasound looks “normal.”


After the urgent issue is addressed, many patients still need a clearer plan for the underlying driver of recurrent ER-level pain. Our team can review your records, make your history “clinically legible,” and discuss whether specialized evaluation and excision surgery may be appropriate—especially if you’ve been dismissed, have persistent symptoms despite prior treatment, or suspect deeper or multi-organ disease.

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How often does imaging miss endometriosis?

Imaging misses endometriosis more often than most patients are led to believe. Ultrasound and MRI can be very helpful for suggesting endometriosis and for mapping certain patterns of disease (like ovarian endometriomas or some forms of deep disease), but a “normal” scan does not rule endometriosis out—especially superficial peritoneal disease, subtle lesions, or disease hidden in difficult-to-visualize locations.


How often it’s missed depends on what type of endometriosis you have, where it is, the scan protocol, and—crucially—the experience of the person performing and interpreting the study. It’s also common for one modality to see something the other doesn’t, because each has different blind spots (for example, bowel gas can limit MRI in some situations, while ultrasound may miss certain deep sites). That’s why our diagnostic process doesn’t hinge on imaging alone; we combine your symptom story, exam findings, and expert imaging interpretation to decide what’s most likely and what the next step should be.


If your symptoms persist despite “negative” imaging, that isn’t a dead end—it’s a data point. Reach out to schedule a consultation so our team can review your history and prior imaging, consider other conditions that can mimic or coexist with endometriosis, and determine whether advanced imaging, further evaluation, or surgical assessment makes sense for your goals.

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Why was more endometriosis found in surgery than on imaging?

It’s very common for surgery to reveal more endometriosis than ultrasound or MRI suggested. Imaging is best viewed as a tool to estimate likelihood and to map certain higher-risk areas for surgical planning—not a reliable “yes/no” detector for every lesion. Many endometriosis lesions are simply hard to visualize on scans because they can be small, superficial, hidden by normal anatomy, or located in areas where imaging performance varies (and where interpretation depends heavily on technique and experience).


Another reason is that scans are better at identifying some patterns—like ovarian endometriomas or certain deep bowel disease—than they are at detecting disease on ligaments, the bladder/anterior compartment, or in complex multi-compartment cases. Imaging also can’t always capture the full extent of adhesions, scar-like tissue, or subtle inflammatory changes that may become obvious only when the pelvis is directly inspected during laparoscopy.


When we plan surgery, we use imaging as one piece of the puzzle alongside your symptom story, exam findings, and overall pattern—because the goal is safe, complete mapping and excision when appropriate. If your operative findings didn’t “match” your scan, it doesn’t mean the imaging was pointless or that your symptoms were exaggerated—it usually reflects the known limits of what scans can show. If you’re trying to make sense of your results or next steps, our team can help you review what was found, what was removed, and what else (like adenomyosis or coexisting pain drivers) may still need to be addressed.

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Normal colonoscopy but bowel symptoms—could it be endometriosis?

Yes—endometriosis can still be a real possibility even if your colonoscopy was normal. Colonoscopy mainly evaluates the inner lining of the bowel (the mucosa), but bowel endometriosis more often lives on the outside of the bowel or within deeper layers of the bowel wall. That means symptoms like pain with bowel movements, cramping, constipation/diarrhea (often alternating), bloating, or even cyclical rectal bleeding can happen while the colonoscopy looks completely “normal.”


In our evaluation process, we focus on the pattern and full constellation of symptoms—especially whether bowel flares track with your cycle or occur alongside pelvic pain, painful sex, urinary symptoms, infertility, or heavy bleeding that can point to coexisting adenomyosis. We often use expertly interpreted pelvic imaging (such as targeted ultrasound or MRI) to help map suspected deep disease and to look for other pelvic conditions that can mimic bowel symptoms or amplify them, like pelvic floor dysfunction, dysbiosis/SIBO patterns, hernias, or vascular compression issues.


If your story fits, our team can help you sort out whether this is bowel endometriosis, endometriosis near (but not inside) the bowel, or another overlapping driver—and what that means for next steps. Because bowel disease is anatomy-dependent and higher-stakes, we prioritize careful pre-op mapping and a plan designed for complete treatment when surgery is appropriate. If you’d like, you can reach out to schedule a consultation so we can review your prior workup and build a clear diagnostic path forward.

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Why do bowel symptoms worsen during my period?

It’s common for bowel symptoms to flare around your period because hormonal shifts can change how the bowel moves and how sensitive the pelvic nerves feel—and if you have endometriosis, those same shifts can amplify inflammation and pain. Endometriosis can affect the bowel directly (often the rectum/rectosigmoid) or irritate the tissues around it, so symptoms can feel “GI” even when the issue isn’t primarily inside the bowel. Scarring and tethering can also pull on the bowel as the uterus contracts during menstruation, making cramping, constipation/diarrhea swings, bloating, or pain with bowel movements more noticeable.


A cyclical pattern—especially pain with bowel movements during bleeding, rectal pressure, or rectal bleeding that tracks with your cycle—raises our suspicion for bowel involvement or deep disease behind the uterus. It’s also why some people have a normal colonoscopy yet still have significant symptoms, since endometriosis often affects the outer bowel surface or deeper layers rather than the inner lining a scope evaluates. If your symptoms are period-linked or progressively worsening, our team can help map what’s going on and talk through next-step evaluation and treatment options, including minimally invasive excision when appropriate.

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Reach Out

Have a question?

Dr. Steven Vasilev delivers best-in-class endometriosis guidance and a personalized treatment plan—built on evidence and your unique biology.


Led by Steven Vasilev, MD—an internationally recognized endometriosis specialist & MIGS surgeon—Lotus Endometriosis Institute is virtual-forward, with many patients traveling nationally for care. Clinical evaluation and surgical treatment are provided in California.

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