Assessing the Implications of a 6 mm Thecal Sac in a 40-Year-Old
Is having a thecal sac of 6 mm considered excessive for someone who is 40? 1. The normal inward curve of the lumbar spine is straightened, accompanied by some advancement in degenerative disc disease at the L4-L5 region, which impacts both transverse L5 nerve roots, with the right side being more affected than the left. It can be anticipated that symptoms would peak in this area, aligning closely with clinical correlations. **EXAMINATION: MRI OF THE LUMBAR SPINE WITHOUT CONTRAST** **EXAM DATE: June 1, 2025, at 6:30 PM** **CLINICAL HISTORY:** Patients report bilateral lower back pain coupled with weakness in the right leg. **TECHNIQUE:** A series of images was procured, including sagittal T1-weighted, sagittal T2-weighted, and sagittal STIR sequences. Axial T2-weighted scans were captured at the segments from T12 to S1. **CONTRAST:** No contrast dye was administered for this procedure. **COMPARISONS:** Recent lumbar spine X-rays taken on April 29, 2025, and MRI scans dated March 18, 2015. **OBSERVATIONS:** **Bone Structure:** The typical lumbar lordosis curvature appears straightened. Overall, the alignment of the vertebrae is intact, and there are no indications of acute fractures or slips. Noteworthy Modic type II changes are present in the endplates adjacent to the L4-5 intervertebral disc, but no alarming marrow signal changes are apparent. No defects in the pars interarticularis are detected. **T12-L1:** No significant deviations. **L1-2:** No significant deviations. **L2-3:** No significant deviations. **L3-4:** Only mild degenerative changes to the posterior facet are observed. There are no signs of central canal narrowing or foraminal constriction. **L4-5:** As previously mentioned, there is a broad disc protrusion and mild degenerative changes at the posterior facets, slightly more pronounced than earlier assessments. This suggests a flattening of both traversing L5 nerve roots (right more than left) and increased crowding among the remaining nerve roots. The AP diameter of the thecal sac is measured at 6 mm, with mild narrowing observed in the left and right neural foramina. **L5-S1:** Only mild degeneration at the posterior facet is noted. There is neither central canal narrowing nor foraminal stenosis. **Conus medullaris:** The conus terminates at the L1 level and appears unremarkable. **Other Findings:** There are no additional observations.
Answers (1)

7/5/2025, 3:30:52 PM
OpenHealth AI
The assessment of a 6 mm thecal sac, especially given your background of lower back pain and neurological symptoms, warrants careful consideration. The most important aspect to recognize is that thecal sac size can vary, and while 6 mm might not be excessive in every context, its implications depend heavily on accompanying clinical symptoms and other MRI findings.
Explanation
-
Thecal Sac and Its Size:
- The thecal sac contains the spinal cord and nerves, providing a protective space for these structures. A typical AP (anterior-posterior) diameter of the thecal sac can vary widely but is usually larger than 6 mm in healthy adults.
- A measurement of 6 mm may indicate some degree of narrowing, particularly in the context of your reported disc degeneration and nerve root involvement.
-
Clinical Correlation:
- Your symptoms of lower back pain and right leg weakness align with the MRI findings of nerve root compression due to disc protrusion and possibly inflammation or irritation around the L4-L5 region.
- This suggests that, while thecal sac size can be a factor, the symptoms and functional impact on your life are what require attention.
Next Steps
-
Symptom Management: Focus on managing your pain and symptoms:
- Pain Relief: Over-the-counter pain relievers (such as ibuprofen or acetaminophen) can help manage pain. Be sure to follow dosing instructions.
- Heat/Ice Therapy: Apply heat or ice to your lower back to alleviate discomfort (15-20 minutes at a time).
-
Physical Activity:
- Engage in gentle stretching and strengthening exercises to improve flexibility and support your spine. Be cautious, and listen to your body to avoid exacerbating symptoms.
-
Monitoring Symptoms:
- Keep track of your symptoms, including any changes in pain intensity, mobility, or neurological symptoms like numbness or weakness. This information can be helpful in any future discussions regarding your care.
-
Considerations for Further Evaluation:
- Depending on how your symptoms evolve, consider whether you might benefit from physical therapy or further evaluation by a specialist such as a spine-focused physiotherapist or a neurologist.
-
Lifestyle Modifications:
- Maintain a healthy weight, incorporate low-impact exercises (e.g., swimming or walking), and ensure proper ergonomics at work and home to reduce strain on your back.
It's understandable to feel concerned given these findings, but many people manage their symptoms effectively through lifestyle adjustments and appropriate care.Continue monitoring your situation, and do not hesitate to revisit any concerns or worsening symptoms with a healthcare professional.
Related Questions
Temple Pain: A Persistent Challenge
Hello everyone. I find myself in a bit of a dilemma and I’m reaching out for advice. I aim to provide as much detail as possible, though previous attempts to explain my condition to medical professionals haven’t gone as smoothly as I hoped. **About Me:** I’m a 19-year-old female, standing at 5’3” and weighing around 180 lbs. My activity levels were once more vigorous, especially as I was an avid dancer and athlete before graduating from high school. **Medical Background:** I’ve been diagnosed with HLA-B27 spondyloarthropathy (the specific type is still uncertain, but it may be either psoriatic arthritis or ankylosing spondylitis). Additionally, I deal with obsessive-compulsive disorder, generalized anxiety disorder, social anxiety disorder, and major depressive disorder. **Current Medications:** I am prescribed 150 mg of Zoloft and Yaz (more for managing acne and heavy menstrual cycles). It's worth noting that I am currently not sexually active, although I’m not sure how relevant this is. **The Main Issue:** For approximately six years, starting around the age of thirteen, I’ve been grappling with a burning or stabbing sensation in my left temple. This pain emerged during a typical school day and has persisted since. Initially, the discomfort would briefly appear and then fade, sometimes going weeks without a recurrence. At that time, I was suffering from severe OCD, which I was unaware of, and fixated on the fear of having a brain aneurysm. I believed that voicing my discomfort would lead to a disastrous outcome. However, when I was prescribed Zoloft in tenth grade for my anxiety, it also began to alleviate my OCD symptoms, enabling me to discuss my pain. A doctor I consulted suggested that it might be migraines—this made sense considering my mother’s history with them. Nonetheless, my experiences with migraines feel distinct; these temple pains are immune to standard over-the-counter medications like Excedrin, Tylenol, or Advil. The only remedies that bring me any relief are applying pressure to the painful spot, using ice, or squinting my left eye tightly. Fast forward to July 2023, when I experienced severe weakness and fatigue, leading to a referral to a rheumatologist who diagnosed me with HLA-B27 spondyloarthropathy. Unfortunately, we haven’t yet found a suitable treatment, so I’m not currently on any medication. I’ve also consulted with a neurologist due to a family history of multiple sclerosis and my struggle with grip strength. While I’ve dealt with chronic pain for as long as I can remember, it was officially diagnosed only after I fell ill in July 2023. Over time, the intensity of the temple pain has increased significantly. It presents as a blend of burning and stabbing sensations, localized solely in my left temple, often accompanied by slight eye pressure. Since those early days in eighth grade, the frequency of these episodes has escalated to daily occurrences, lasting from several hours to days. The pain has even disrupted my sleep, and today, my trusty ice pack failed to provide any relief. I’m not quite sure what I hope to achieve from this post; I just feel utterly drained by this situation. I’m reaching out as a last resort, especially since my neurologist brushed my concerns aside. It feels like I’m on the verge of losing my grip on things. Thank you for taking the time to read my story. I appreciate your understanding. With love 🩷
Severe Skin Burn After Using Glycolic Acid Post-Electrolysis
Recently, I applied glycolic acid to my skin following an electrolysis session just a few days prior. Unfortunately, this led to a significant burn that is incredibly painful. While the burn may not appear severe in images, the discomfort is intense, and distressingly, there has been no sign of improvement for over a week. I sought medical attention, but the only guidance I received was a prescription for antibiotics from my dermatologist, intended to ward off any potential infection. My concern lies in the possibility that the acid seeped into the hair follicles, causing deeper burns beneath the surface, while the outer layer of skin appears relatively unaffected. I'm feeling lost about the next steps and anxious about how long it might be before I notice any recovery. **Personal Details:** - Age: 25 - Gender: Male - Height: 5'8" - Weight: 130 lbs (58 kg) - No major health conditions; not on any heavy medication.
Is It Common to Experience a Persistent Mild Cough Post-Mycoplasma Pneumonia?
I've been battling a severe cough for about a month, which led to a diagnosis of mycoplasma pneumoniae through blood tests. Thankfully, my chest X-ray was clear. The cough was incredibly wet, producing an astonishing amount of clear phlegm, with multiple coughing fits throughout the day, which felt overwhelming. After completing my antibiotic treatment, I felt much better and was able to return to my normal activities. Yet here I am, 2.5 months post-treatment, with a minor but persistent cough that refuses to fade. The amount of phlegm still seems excessive, and I occasionally experience short periods where the cough intensifies for a day or two. Additionally, I find myself sweating randomly every now and then. **Is it typical to have a mild, lingering cough after recovering from mycoplasma pneumoniae?** For context, I've had pneumonia in the past, and even after proper treatment, I dealt with random sweating episodes for about five years. So, I can't help but wonder if the sweating I'm currently experiencing is something to be concerned about or just another aftereffect of my respiratory issues. A bit about me: I'm a 30-year-old male, stand 6'2" tall, I do not take any medications, and I do not smoke.
Recurring Throat Abscesses After Tonsil Removal: What's Going On?
At 27 years of age, I underwent tonsillectomy 11 years back due to frequent strep throat episodes. For a long time, I enjoyed good health without any throat problems, until earlier this year when I began experiencing intermittent sore throats, predominantly on one side. These discomforts typically lasted a few days before resolving on their own, so I didn't think much of them. However, last month, I awoke with severe pain and swelling in my throat, making it difficult for me to speak. Upon inspecting my throat in the mirror, I noticed pus oozing from the area where my tonsils used to be, which caused me significant alarm. I immediately resorted to gargling salt water, which provided quick relief. Unfortunately, this morning I encountered a similar situation, but this time the discomfort had shifted to the opposite side of my throat. It seems that these abscesses are somehow draining spontaneously when I open my mouth widely. Generally, I consider myself to be a healthy and active individual, with no significant dental problems aside from this troubling issue. I find myself increasingly anxious about the possibility of this becoming a recurring condition. As I'm currently without health insurance, seeking help from an ENT specialist in my locality would be quite costly. Could these symptoms be indicative of peritonsillar abscesses or could there be another underlying issue?
Dealing with Unwanted Erections Linked to IBS Flare-Ups
Greetings everyone, I'm a 23-year-old male grappling with Irritable Bowel Syndrome (IBS), and I’m looking for some guidance regarding a perplexing issue I face. Whenever I experience a flare-up of my IBS and begin to sense impending bowel movements, I invariably find myself dealing with an erection. This occurrence is often uncomfortable and distinctly heightened. I suspect that this reaction may stem from heightened blood circulation in my pelvic region or the connections with surrounding muscles. Nevertheless, this situation significantly detracts from my overall well-being, and I haven’t found much support from either my primary care physician or my gastroenterologist. Is there anyone else out there who has encountered a similar predicament?