23F. Tumor Found in Liver During Ultrasound: Seeking Clarity
I'm a 23-year-old female, standing at 177 cm and dealing with being overweight. My daily medication routine includes venlafaxine and bisoprolol, along with a monthly dose of Ajovy. Occasionally, I take Vyvanse, quetiapine—primarily for sleep—and frovatriptan as necessary. For joint discomfort, I rely on over-the-counter options like naproxen or paracetamol. I suffer from chronic migraines and have developed dysautonomia along with ME/CFS following a COVID-19 infection in 2022. I've also been diagnosed with ADHD. A physiatrist identified hypermobility spectrum disorder (HSD) after a test showed I fell short of the criteria for hypermobile Ehlers-Danlos syndrome (hEDS) by one point. Additionally, I struggle with an anxiety disorder, depression, and I have a complicated history with eating disorders. My menstrual health has fluctuated between oligomenorrhea and amenorrhea, prompting me to see an OBGYN who specializes in endocrinology. Recently, I was diagnosed with hypothyroidism after being considered to have subclinical hypothyroidism for years. An endocrinologist has now prescribed me thyroxine. Notably, diabetes, various rheumatic conditions, ankylosing spondylitis (AS), Chiari malformation, and sleep apnea have all been ruled out. Imaging of my brain and neck in 2022 returned normal results. However, my ESR and CRP levels have remained slightly elevated over the past three months. Tests for insulin resistance and polycystic ovary syndrome (PCOS) are forthcoming; I had documented at least ten cysts on my left ovary, while the right ovary wasn't evaluated thoroughly during the last visit. Earlier this week, I had an ultrasound to examine my liver and other upper abdominal organs, primarily to assess for non-alcoholic fatty liver disease (NAFLD) due to persistent elevation in certain liver markers—specifically, my ALT was recorded at 55, where the reference range is under 35 U/l. During the ultrasound, a dark round spot was visible on my liver, and even I could see it on the screen. The technician mentioned that considering my age, it appeared to be likely benign. The initial report indicated it was probably a hemangioma, suggesting that further imaging was unnecessary. However, just a few days later, a different physician provided an updated assessment: "...The liver parenchyma exhibits slightly increased echogenicity with fat, and there is no sign of degeneration. Nonetheless, a measured 4 cm diameter area shows patchy changes with a more hypoechoic appearance relative to the surrounding liver, displaying effective contours and a meandering pattern; this finding is atypical for a hemangioma and suggests further evaluation of focal liver changes through cross-sectional imaging alongside enhancement techniques..." I'm not seeking a diagnosis, but I’m curious about potential tumor types that this could represent and the next actions if it turns out to involve a tumor. What might "effective contours" and “meandering” indicate? Is there a chance it could signify a more serious condition? Notably, I currently have no symptoms that would typically align with liver issues.
Answers (1)
7/19/2025, 8:01:46 AM
OpenHealth AI
It's understandable to feel concerned after discovering a liver lesion during an ultrasound. While the initial report suggested a benign hemangioma, the updated assessment raised questions about the nature of the lesion. Here’s a breakdown of key points and next steps:
Key Points
-
Types of Liver Lesions: The dark round spot seen on your liver could represent various conditions, such as:
- Hemangioma: Typically benign and composed of blood vessels.
- Focal Nodular Hyperplasia (FNH): A benign liver tumor that can resemble hemangiomas.
- Hepatic Adenoma: A benign tumor that may occur in women, often associated with estrogen.
- Malignant tumors: Such as hepatocellular carcinoma, though this is less common, especially in younger individuals without risk factors.
-
Interpretation of Terms:
- Effective contours: This usually means the edges of the lesion are well-defined, which can indicate a benign nature.
- Meandering pattern: This suggests irregularities in the structure, which can warrant further investigation.
-
Potential Seriousness: While many liver lesions prove benign, the description you've provided might warrant further evaluation to rule out any malignancy.
Next Steps
-
Follow-Up Imaging: Since the updated report suggests atypical characteristics, it’s crucial to undergo further imaging as recommended, such as a CT scan or MRI. These techniques provide a more detailed view of the lesion and might include contrast to assess how the lesion enhances, which can help in determining its nature.
-
Monitoring Symptoms: Keep track of any new symptoms that may arise, although you mentioned having none currently aligned with liver issues. Symptoms to watch for might include unexplained weight loss, jaundice (yellowing of the skin/eyes), or abdominal pain.
-
Discuss with Your Doctor: Schedule a conversation with your healthcare provider regarding the importance of the follow-up imaging, what the findings may imply, and what treatment options might be available depending on the results.
-
Stay Informed and Supported: Continue to educate yourself about liver health, but also consider support groups or counseling, given your history with chronic conditions and mental health. This can help in managing anxiety related to the uncertainty.
-
Adopt a Healthy Lifestyle: Try to maintain a balanced diet and regular physical activity as tolerated, as these can support your overall liver health and general well-being.
Your concern is completely valid, and seeking further information is a responsible approach. Remember to keep communication open with your healthcare team and follow their recommendations closely. Let me know if you need additional clarification or further assistance!
Related Questions
Understanding Possible Seizure Triggers and Recurrence Risks
Health Background: I am a 21-year-old female, standing at 169 cm and weighing 65 kg. Over the past three years, I have been using oral contraceptives. As of this morning, I started taking 25 mcg of levothyroxine along with a weekly vitamin D supplement of 0.266 mg. Recently, I was diagnosed with hypothyroidism and found to have a vitamin D deficiency that I suspect has existed for the last three years. I do not consume alcohol or smoke, and I can confirm I am not pregnant. Two years ago, I experienced a mild concussion. I currently reside in Spain. A couple of months back, in mid-December, I blacked out twice. The second occurrence took place while I was at the doctor’s office after seeking urgent medical care for the initial incident. Following the second episode, I underwent a CT scan and an EKG, both of which returned normal results. Further tests, as directed by my physician, revealed a critical vitamin D deficiency and hypothyroidism; however, he expressed doubt that either of these conditions led to my loss of consciousness. I was then referred to a neurologist, and I am presently awaiting an appointment. Although the waiting period is lengthy, my doctor indicated that I should receive priority for scheduling, although the exact timeframe remains uncertain. The referral document summarized my events, labeling the second episode (which the physician witnessed) as a potential seizure devoid of tonic-clonic movements—a revelation that took me by surprise. After regaining consciousness, I felt extremely disoriented and terrified, struggling to process what was happening. I have no prior history of seizures, epilepsy, or any related conditions, and there is no known family history of these issues. If this indeed was a seizure, what might have triggered it? Additionally, what is the likelihood of experiencing another one? Since that time, I have not had any further incidents, but I have experienced moments where I felt a sense of impending doom, which I managed to overcome. I intend to wait for the neurologist's evaluation, but the uncertainty surrounding a possible neurological condition is quite distressing. Thank you for any insight you can provide!
Persistent Pain in Right Shoulder and Arm After Lifting
Hello, everyone! I’m a 23-year-old male and have been engaged in weightlifting for several years now. Recently, I’ve been struggling with ongoing discomfort in my right shoulder and arm, which I haven’t been able to accurately identify. The pain manifests during particular movements, especially with lateral raises or when my arm is raised to shoulder level while rotating my wrist. Certain pressing and pulling activities can also provoke this discomfort. Rather than feeling sharp, it’s a deep, nagging sensation that sometimes seems localized in the front area of the shoulder or at the biceps tendon, and at other times it feels more like it’s situated between the shoulder and upper arm. Fortunately, there’s no numbness or tingling involved. This issue began while I was working out. I decided to take a break for around two months, but when I returned, the pain persisted. After consulting a physician, I was diagnosed with bicipital tendinitis. Since then, I’ve reduced my upper-body workouts, completely steering clear of shoulder exercises and heavy lifting, and have begun a gentle rehabilitation regimen focusing on external rotations, pendulum movements, and scapular exercises. Despite adhering to this routine for about a week, I haven’t experienced any noticeable improvement. Is it typical for this type of tendon injury to require an extended period for recovery? At what point should I consider diagnostic imaging, such as an ultrasound or MRI? Additionally, are there frequent rehabilitation errors that might impede the healing process? I appreciate your insights in advance!
Understanding EEG Results for My 22-Month-Old Son: Insights Needed
Could someone help clarify this for me? My son, who is just 22 months old, hasn’t started walking yet, becomes tired easily, and has been experiencing behavioral outbursts. He had a febrile seizure in February 2025, followed by another unexplained seizure in April 2025, which led us to consult a neurologist. Since he was 3 months old, he has been receiving therapy from a physical therapist for torticollis. At birth, he spent five days in the NICU due to issues with meconium aspiration. A recent MRI showed normal results, and he also had a follow-up EEG after one conducted in July 2025. The results from this recent EEG were abnormal for a pediatric patient in awake, drowsy, and sleeping states. Notably, there were brief episodes of left frontotemporal delta slowing, which occurred mainly when he was awake and drowsy. There were no signs of epileptiform activity detected. In contrast, the EEG performed back on July 3, 2025, was deemed normal for both awake and drowsy states, again with no evidence of epileptiform irregularities, although it did not capture any sleep data. This examination was prompted by the child's existing history of febrile seizures. Importantly, he is not currently on any anti-seizure medications. The EEG procedure used standard electrode placements per the 10-20 system, conducted a single-lead EKG, and included continuous video monitoring. During the analysis, the background activity was symmetric, indicating some anterior-posterior (AP) organization, with a dominant rhythm of 50-80 microvolts at 7 Hz. His drowsy state was marked by a reduced amount of eye blink activity, less breathing motion interference, and a generalized slowing in theta/delta frequencies. Stage II sleep exhibited spindles and vertex waves patterns. Additionally, there were intermittent bursts of 250-300 microvolts in the left frontotemporal region with semi-rhythmic activity of 2-4 Hz, mostly observed during wakefulness and drowsiness. No definitive epileptiform discharge was noted. Photic stimulation during the test did not elicit a strong response, and hyperventilation was not conducted during this session.
INTENSE Spine Discomfort, Breathing Difficulties, Muscle Twitches, and Sweating
To elaborate on the situation mentioned in the title, I’ve been experiencing unusual muscle twitches and spasms for the past few days, along with some discomfort in my back. However, today, I felt an unexpected sharp pain shoot through my spine, which has left my legs feeling numb and made it impossible for me to sit up straight. Additionally, I’ve been dealing with cold sweats for the last hour and struggling to breathe properly. Perhaps I’m just overanalyzing things and it’s a common occurrence, but the intensity of the pain is overwhelming—it's truly unbearable. I’m shaking quite a bit, and unfortunately, my parents aren’t responding to my attempts to reach them for help. I have a history of a chronic heart condition and arthritis, yet I’ve never experienced pain this severe, especially in my spine. For context, I am nearly 15 years old and female. My current medications include pain relievers, anxiety medication, beta blockers, and some vitamins, though those specifics may not be particularly relevant. I don’t smoke; however, I have tried vaping a few times, which might not matter much, but I thought it was worth mentioning as it was requested.
Understanding Atrial Fibrillation and Thyroid Issues: Variability in Cardioversion Decisions
Hello everyone, I’m reaching out for guidance regarding my mother’s current health situation, and I’d greatly appreciate any shared experiences or thoughts. **My mother's background:** - **Age**: 55 years - **Weight**: Recently dropped to 116 kg from 118 kg in just two days, likely due to diuretics. - **Health history**: Previously an underactive thyroid, undiagnosed and untreated, now presenting as overactive. - **Medications**: Currently taking thyroid medication and a beta-blocker (Rapiblock). **Current health status:** My mother has been hospitalized since Tuesday, experiencing **atrial fibrillation with heart rates exceeding 200** beats per minute due to her thyroid's hyperactivity. - The plan for cardioversion was initially settled on Tuesday. However, the following day, the medical team advised postponing it until her thyroid levels could be stabilized, believing that her heart rate would return to normal once her thyroid condition was managed. - Her **obesity** precludes her from undergoing a transthoracic echocardiogram, and due to her thyroid concerns, she cannot handle contrast dye (this has been a consistent issue for over four years). Therefore, the only feasible option was a **transesophageal echocardiogram (TEE)**, which has yet to be performed. - She has been prescribed various medications including beta-blockers and thyroid treatments in the past. - On Friday, a doctor proposed proceeding with cardioversion; however, the attending senior physician objected. - Today (Saturday), another clinician has expressed a desire to move forward with cardioversion, having initiated a new medication, as the senior physician is unavailable. - **Communication has been unclear**, as we were notified of developments by a nurse rather than the physician in charge, causing confusion and anxiety. - Currently, only a **chest X-ray** is scheduled, and the TEE remains unaddressed. **My inquiries are as follows:** 1. Is it common for medical professionals to have varying opinions and frequently revise medication or treatment plans like cardioversion? 2. Is it safe to conduct cardioversion in the absence of a TEE? I presumed that this was a standard procedure to exclude the presence of blood clots. 3. Is it usual practice to have only a chest X-ray prior to moving ahead with cardioversion? 4. How typical is it for patients or their families to not be directly informed about treatment changes and learn about them through nursing staff instead? I recognize that this cannot substitute for professional medical advice. I’m simply trying to discern whether these circumstances are typical or if we should express our concerns more assertively with the healthcare facility. Thank you for your insights!