OpenHealth Q&A

Get answered by medical professionals

Are These Ultrasound Results Indicative of Endometriosis?

7/28/2025, 6:40:28 PMMale25-34

A 26-year-old female acquaintance of mine is undergoing evaluation. She has never engaged in sexual activity, and her physician has already discounted the possibility of Pelvic Inflammatory Disease (PID). Despite this, I remain unconvinced by a diagnosis suggesting a chocolate cyst; I find it more plausible that it is a hemorrhagic cyst instead. Can a chocolate cyst truly be identified based solely on a single ultrasound examination? The only issues she reports are light spotting occurring about a week after her menstrual periods, accompanied by mild pelvic discomfort during the spotting episodes. Her menstrual cycles themselves are not particularly painful, and she notes that her experience has been consistent over time.

Crohn's DiseaseThyroid DisordersEndocrinology

Answers (1)

Cony

7/28/2025, 6:40:46 PM

OpenHealth AI

The ultrasound results you mentioned raise important considerations regarding the diagnosis of endometriosis and the type of ovarian cyst present. It’s essential to understand what a chocolate cyst is and how it can occur, as well as the limitations of ultrasound in making definitive diagnoses.

Key Points

  1. Chocolate Cysts vs. Hemorrhagic Cysts: A chocolate cyst, also known as an endometrioma, is a type of ovarian cyst formed when endometrial tissue grows on the ovary, leading to a cyst filled with old blood. Hemorrhagic cysts are fluid-filled sacs that may bleed but do not have the same association with endometriosis.
  2. Ultrasound Limitations: While ultrasounds can suggest the presence of chocolate cysts, they are not always definitive. The imaging can provide clues, but a single ultrasound may not clearly distinguish between different types of cysts, especially in the absence of more distinctive signs.
  3. Symptoms Consideration: Light spotting after periods and mild pelvic discomfort are nonspecific symptoms that can align with various conditions, including hormonal fluctuations or benign cysts, not just endometriosis.

Next Steps

  1. Observe Symptoms: Continue to monitor any changes in her symptoms, particularly if the spotting becomes heavier or more frequent, or if discomfort increases.
  2. Follow-Up Imaging: If there's uncertainty or if symptoms worsen, consider scheduling a follow-up ultrasound or possibly an MRI, as these can provide additional insights into the nature of the cyst.
  3. Discuss Options: Engaging in a conversation with her physician about these observations and any concerns is essential. If endometriosis is suspected due to ongoing symptoms, further evaluation might be warranted, even if she's not experiencing typical endometriosis-related pain.

Encouraging her to prioritize her health and seek clarity with her medical provider is crucial. Both the patient and her healthcare team can make informed decisions based on her symptoms and diagnostic findings moving forward.

Related Questions

Navigating Uncertainty: Symptoms and Concerns

I am a 35-year-old male, standing at 6 feet 3 inches tall and weighing 190 pounds, with a family history that includes stroke and diabetes. This explanation may be a bit lengthy, but I want to be thorough. Over the last four months, I've been experiencing a consistent but mild ache in my neck and shoulder. Initially, the discomfort was rated around a 4 or 5 out of 10—significant enough to be bothersome, yet not enough to severely limit my daily activities. Recently, this pain has diminished to about a 2 or 3, but it has become a constant presence. Two months ago, I encountered a troubling episode where I felt dizzy and noticed my heart racing, which led me to believe that I was facing a serious health crisis. Upon visiting my doctor, the assessment suggested I might have an upper respiratory infection and some associated inflammation. However, I found it concerning that no MRI or similar diagnostic imaging was ordered, nor were any substantial tests performed, including blood work. Typically, I would expect antibiotics for something like a URI, yet that was not the course of action taken. A month later, I consulted a physician at a free health clinic, where I was informed that I had likely strained a muscle connecting my shoulder to my neck. Although two to three months seems like an extended period for such a strain, I tend to avoid self-diagnosis. Once again, I was prescribed Aleve without any concrete tests being conducted and was simply advised to manage the pain. The doctors were vague about the source of inflammation, only instructing me to continue taking Aleve. Since then, I haven’t experienced any episodes of dizziness or rapid heartbeats; however, the soreness in my shoulder and neck persists. Additionally, I’ve noticed a small, circular rash, measuring about an inch in diameter, on the right side of my chest near the collarbone. This rash has no associated itching or pain but made its appearance only after I started feeling what I describe as "unwell." Given this ongoing discomfort and the various symptoms, I’m left questioning whether I’m dealing with an infection, musculoskeletal issues, or something else entirely.

DiabetesArthritisCrohn's Disease
Male25-34
14 minutes ago

Seeking Guidance on Finding the Right Hematologist/Oncologist

My husband recently received a recommendation to consult a Hematologist/Oncologist from his Allergist, and I find myself feeling quite lost in the process. He is 45 years old and has been living with mastocytosis, which has been functioning predominantly in a cutaneous manner for around a decade (diagnosed in adulthood). We thought it was manageable and chose to overlook it. Approximately ten years ago, he visited a Hematologist/Oncologist who examined his tryptase levels and decided that a biopsy was unnecessary, which brought us some relief at the time. However, about two months ago, he unexpectedly encountered gastrointestinal issues, prompting us to take the situation more seriously. His Allergist recommended a Hematologist/Oncologist to facilitate a bone marrow biopsy. When he reached out to the office specified in the referral, they informed him that they do not perform bone marrow biopsies in-house, but instead outsource them. Is this common practice? If this is how it usually operates, will we need a separate referral for the physician conducting the biopsy? If the Hematologist/Oncologist does not execute these procedures, is it truly necessary to have one? After all, in oncology, one would presume that handling cancer cases would take precedence over merely coordinating referrals. Unless it turns out that my husband’s mastocytosis has progressed to a stage requiring chemotherapy—information we can only ascertain through a biopsy—this situation is confusing. I had thought oncologists were consulted when cancer is confirmed, rather than when one is uncertain. Furthermore, is there a specialized database for locating doctors? While perusing options on WebMD, I noticed that many physicians listed particular expertise areas, including breast cancer or various gastrointestinal conditions, yet mastocytosis was not mentioned. Does this absence of focus matter in our selection process? Should I consider a physician who is focused on leukemia, even though that feels like a stretch given my husband’s condition? Is it appropriate to see a physician solely for a biopsy and then seek someone else for ongoing care after receiving results, simply because one desires specialized expertise in a different area? This idea strikes me as somewhat inconsiderate. Truthfully, I am currently open to finding any doctor who exhibits genuine interest in mastocytosis and can perform a bone marrow biopsy. After we obtain the necessary information, I would prefer to secure the best possible specialist that my insurance would accommodate. I would greatly appreciate any insights you may provide. I feel overwhelmed by the complexity of this process but am still expected to navigate these significant choices.

Multiple SclerosisLupusCrohn's Disease
Male25-34
24 minutes ago

Seeking Insights on Unexplained Neurological Symptoms

I am a 34-year-old woman grappling with a complicated and deteriorating array of neurological issues, and I am in search of guidance or advice. After consultations with a neurologist who has expertise in multiple sclerosis, I am left without a definitive diagnosis or treatment strategy, despite several alarming findings. **Symptom Progression:** My neurological function has been steadily declining over the past few years. In late 2024, I experienced a sudden increase in severity of symptoms, leading to an emergency hospitalization where I required catheterization due to urinary retention, a situation I had faced previously but never to this extent. This incident prompted a thorough evaluation for acute neurological deterioration. Since then, my healthcare providers have observed a progressive decline in mobility; I now rely on a walker and sometimes a wheelchair. My medical documentation reflects issues such as urinary urgency, retention, elevated post-void residual volumes, increasing weakness in my legs, changes in vision, and cognitive challenges. These symptoms have heavily influenced my everyday life and are currently the focus of an ongoing clinical evaluation. **Notable Diagnoses:** - **Brain MRI (December 2024 & January 2025):** Revealed a small stable hyperintense lesion in the periventricular area, near the posterior body of the lateral ventricle. The neurologist believes it may not be significant enough to indicate MS. - **Spinal MRI:** Suggests the presence of a possible intramedullary lesion at the T7-T8 level, coupled with a herniated disc. **Cerebrospinal Fluid Analysis:** - Eight oligoclonal bands present exclusively in the cerebrospinal fluid. - Mildly elevated white blood cells suggesting lymphocytic pleocytosis. - Evidence of macrophages and lining cells. - Low glucose levels. - All tests for infections and autoimmune disorders returned negative. **Additional Context:** My neurologist has considered the possibility of a neuroinflammatory disorder but concluded that there is insufficient evidence to confirm MS, primarily due to the size and quantity of the lesions. Other potential conditions such as neurosarcoidosis, infections, or systemic autoimmune disorders have been excluded following comprehensive laboratory assessments. An MRI conducted in 2014 showed the same lesion with no changes, implying that it has been present for a significant duration. I am willing to commence treatment even in the absence of a conclusive diagnosis to stabilize my current functions. **My Inquiry:** What alternative diagnoses might be possible if not multiple sclerosis? Has anyone dealt with a comparable case featuring positive oligoclonal bands, a periventricular lesion, and a progressive symptom profile without a clear diagnosis? Are there any neuroinflammatory disorders that might manifest in this way yet do not fulfill the McDonald criteria? Any insights, suggestions, or recommendations for my situation would be greatly appreciated. Thank you for your time.

Multiple SclerosisLupusCrohn's Disease
Male25-34
1 hour ago

Seeking Insights on My Brain MRI: Early Hypoxia and Developmental Challenges

Greetings. I am a 20-year-old individual who has faced various developmental challenges, both physical and cognitive, since I was a child. It has been reported that I was born with a hypoxic condition and exhibited paroxysmal activity on my EEG during my younger years. Additionally, I have endured significant physical and emotional abuse throughout my upbringing, which I believe has had a detrimental impact on my neurological and psychological growth. Currently, I continue to face several difficulties, including: - Motor function issues on my left side (affecting both my leg and hand) - Cognitive delays - Challenges with emotional regulation and a heightened state of alertness Recently, I came across a brain MRI from 2021 (T2-FLAIR), but I do not have access to a neurologist at the moment. I would greatly appreciate it if someone could review the MRI and point out any notable findings, particularly those suggesting potential early hypoxic damage or trauma-related changes in the brain. I am not seeking a formal diagnosis; rather, I am looking for insights that could aid me in my healing and personal growth journey. Thank you for your consideration.

Multiple SclerosisLupusThyroid Disorders
Male25-34
1 hour ago

Inquiry About Hematology Results

Hello! I'm a 25-year-old woman, standing at 5'5" and weighing 250 pounds. I underwent gastric sleeve surgery in March of 2025, and I've been diligent with my vitamin and supplement intake since then. For some time, I’ve observed that my hemoglobin and hematocrit levels have been consistently elevated. My white blood cell count, red blood cell count, and platelet levels, however, tend to fluctuate more frequently. Meanwhile, my iron levels have ranged from low to normal. Given that my hemoglobin (normal values: 11.5 - 14.5 g/dL) and hematocrit (normal values: 35.0 - 43.0 %) are higher than the ideal range, should I consult a hematologist? Here are my hemoglobin readings: - July 22, 2025: 15.8 g/dL - July 17, 2025: 15.8 g/dL - June 4, 2025: 16.1 g/dL - May 17, 2025: 15.8 g/dL - March 19, 2025: 15.8 g/dL - February 24, 2025: 14.9 g/dL - August 31, 2024: 14.7 g/dL - August 9, 2024: 14.8 g/dL - February 23, 2024: 15.6 g/dL And for my hematocrit: - July 22, 2025: 46.2% - July 17, 2025: 47.7% - June 4, 2025: 47% - May 17, 2025: 46.2% - March 19, 2025: 46.9% - February 24, 2025: 43.7% - August 31, 2024: 44.2% - August 9, 2024: 43.5% - February 23, 2024: 46.6% I'm eager to hear your thoughts on whether I should seek specialist advice regarding these findings.

Thyroid DisordersInternal MedicineRheumatology
Male25-34
1 hour ago