Rheumatoid Nodule with Bruising: Should I Be Concerned?
I’m a 36-year-old woman weighing 135 pounds, and I have been diagnosed with rheumatoid arthritis (RA). Recently, my rheumatologist identified a rheumatoid nodule located on the back of my hand. A few days ago, I began experiencing some discomfort and tenderness in that area, which was unusual for me. Then, just yesterday, I observed a bruise forming right above the nodule. This bruise doesn’t seem to be superficial; it appears to be a deeper bruise that's surfacing under the skin. I find myself questioning whether this is a common occurrence with RA nodules, or if there could be a connection at all. It’s worth noting that I haven’t injured my hand or subjected it to any trauma recently. Now, I’m torn between contacting my rheumatologist promptly or waiting a few days to see if the situation improves on its own. However, I can't shake off the feeling of anxiety about it. I would genuinely appreciate any insights or advice on this matter! 🙏
Answers (1)

8/7/2025, 9:40:43 PM
OpenHealth AI
It's understandable to feel anxious about new symptoms, especially with rheumatoid arthritis (RA) involved. The appearance of a bruise and discomfort near a rheumatoid nodule may warrant some attention, but it doesn't necessarily mean there's a serious issue.
Key Points:
- Bruising and tenderness near a rheumatoid nodule can occur, especially due to inflammation related to RA.
- It’s important to monitor your symptoms, especially as they can occasionally indicate changes that need attention.
Explanation: Rheumatoid nodules are common in individuals with RA and can sometimes be associated with inflammation or pressure in that area. While bruising is less typical without trauma, it can occur if there's underlying inflammation affecting blood vessels near the nodule, possibly leading to spontaneous bruising. However, new or worsening symptoms in conjunction with existing conditions should always be taken seriously.
Next Steps:
- Monitor Symptoms: Keep an eye on the bruise and any changes in the discomfort or tenderness. Look for signs of increased swelling, warmth, or if the bruise expands or doesn't improve over the next few days.
- Pain Management: If you're uncomfortable, consider using over-the-counter pain relief like acetaminophen or ibuprofen, as appropriate (following dosing instructions).
- Contact Your Rheumatologist: Given your ongoing RA and the new symptoms, it would be wise to reach out to your rheumatologist for advice, especially if the discomfort increases or the bruise worsens over the next few days.
Acknowledging your concerns and taking proactive steps will help you manage your health more effectively. Please let me know how you're doing or if you have further questions!
Related Questions
Managing Loose Scar Tissue in a 64-Year-Old Woman's Heel
My spouse, aged 64, has developed a considerable amount of loose scar tissue within her heel, a remnant from an injury sustained many years ago. Imaging results indicate that this tissue is not connected to any bones or tendons. We are unsure which medical specialist should be consulted for the surgical procedure or the specific term for this type of surgery. Could the removal of this scar tissue result in any deformities to her heel? Will the heel be capable of healing and regenerating new tissue to fill any gaps left by the excised scar? We are eager to find a solution as the site of the old injury occasionally reopens and becomes infected.
Can Disuse Osteopenia Be Reversed?
I am a 44-year-old woman who experienced a severe injury at 38, specifically a displaced comminuted fracture in my wrist affecting the distal radius and ulna. This injury resulted in my wrist being immobilized multiple times for extended periods. Over the next three years, I underwent three surgeries, which included two osteotomies and numerous procedures to repair adhesions. Eventually, this led to a diagnosis of disuse osteopenia in my radius due to prolonged immobilization. Currently, I have resumed normal use of my wrist, but I still notice some limitations. My fingers lack their previous speed and strength, I have not fully regained sensation, and the range of motion in my wrist is somewhat diminished. However, I can manage to carry objects without difficulty with that arm. I am curious if disuse osteopenia can actually be reversed. What is the likelihood that my bone density has improved to a level close to what it was before the injury? Additionally, am I at risk for developing osteoporosis in that specific bone?
Concerns About Painful Axillary Lymph Node
I’m seeking guidance and perhaps a bit of reassurance regarding a troubling health issue. Here’s the situation: A 57-year-old woman began experiencing intermittent pain in one of her axillary lymph nodes about a month ago. Over time, the discomfort worsened and was accompanied by fatigue, dizziness, as well as minor variations in body temperature and blood pressure. Following this, she consulted a doctor who, upon conducting blood tests (including a CRP test, all of which returned normal results), found no alarming signs. However, a course of Ceporex (Cephalexin) at a dosage of 1 gram for ten days was prescribed. An ultrasound was performed, producing the following results: - Normal appearance of skin, areola, and subcutaneous layers. - Both breasts exhibit primarily fibroglandular tissue. - There are no solid or cystic formations. - No distortions in the architectural layout. - The ductal system is normal. - Absence of malignant calcifications in the breast on either side. - No indications of malignant lymphadenopathy in the axilla on either side. - Right axilla: Notable is one ovoid lymph node with central cystic breakdown, measuring 16 x 10 mm. **Assessment:** Indications of breast fibroadenosis, categorized as BIRADS 2, along with a right axillary lymph node showing inflammation as described. Following this, the doctor prescribed Tavacin 500 mg for a period of five days instead of continuing with Ceporex, and scheduled a follow-up ultrasound for a week later. The repeat ultrasound demonstrated: ✅ Normal skin and tissues. ✅ No solid or cystic masses. 🔄 A few reactive lymph nodes on the right side, with none being suspicious on either side. 🟡 One lymph node in the right axilla (the painful one) presented with the following characteristics: - Ovoid shape - Exhibits central cystic breakdown - Dimensions of 16.3 × 9.4 mm, quite similar to the previous measurement of 16 × 10 mm. **Conclusion:** Atypical lymph node maintaining a stationary progression. Due to the persistent pain and discomfort, we sought a second opinion. The dizziness has ceased, which is a relief. The second doctor advised us to cease all antibiotics and monitor the situation for two weeks before repeating the ultrasound. If the situation remains unchanged, a biopsy will then be considered. What could this condition potentially indicate? It’s worth noting that she was the caregiver for a patient with Klebsiella MDR a while back. Although there was contact with some of the patient's items at the onset of her symptoms, she consistently wore gloves and a mask during that period.
CT Scan Reveals Mesenteric Panniculitis – Could This Be Related to My Symptoms?
**19-year-old male from Brazil.** I am currently anticipating my follow-up appointment with the rheumatologist, which is set for the 3rd of next month. The medical professionals have opted not to prescribe any anti-inflammatory drugs at this point, as they wish to accurately identify the underlying condition affecting me. Presently, there is a strong suspicion that I may have Behçet’s disease. My symptoms include arthritis, persistent low-grade fevers, repeated oral lesions, cutaneous manifestations, swollen lymph nodes throughout my body, and a significant rise in CRP levels (greater than 50 mg/L). I also have a past occurrence of genital ulcers from two years ago, neurological symptoms like seizures and weakness in my legs, along with spider veins. Interestingly, I am also experiencing discomfort and coldness in the toes of my left foot, though the cause of this is unclear. I am curious whether the diagnosis of panniculitis might prompt the doctors to consider medication options sooner. In the meantime, I have taken matters into my own hands and used some of my mother's diclofenac sodium tablets, which have alleviated some of the swelling in my joints. At this moment, I don't believe I need to visit the emergency department, but I'm worried about my mental state as I try to cope with this level of pain until my next appointment at the end of the month.
F25. Questioning the Future of My Progressive Condition
**F25.** Height: 176 cm, Weight: 124 kg. I have multiple disabilities, marked by a gradual decline in my mobility that started around age 15. My symptoms resemble those of a neuromuscular disorder, but I also deal with issues related to my connective tissue. On the mental health front, I've received thorough evaluations and treatments. My ADHD management with Atomoxetine is effective, and those around me are understanding of my autism. I've undergone trauma therapy, enabling me to cope with my trauma-related conditions. Furthermore, my adolescent psychosis has remained in remission since I was 19, with no relapses. As a child, I was quite clumsy and uncoordinated—never the athletic type. I could run, jump, or climb, but not as adeptly as my peers. My struggles were often brushed off as just quirky behavior. While I did experience some vague physical complaints, they were overshadowed by the abuse I endured, which made it difficult to determine their severity. By the ages of 12 to 13, these vague discomforts and exhaustion escalated, yet they remained too ambiguous for others to address seriously. At 15, I could still perform everyday activities like standing, walking, and climbing, but I started noticing an increase in my falls and challenges with physical exertion. Fast forward to 20—I lost the ability to run, jump, or climb. Walking short distances became a struggle despite using mobility aids like crutches and a rollator. My walking ability further declined, with the rollator proving useful for only about ten months. By age 21, I transitioned to a manual wheelchair followed eight months later by a power wheelchair. By 23, I was unable to sit in my power wheelchair and became bedbound while awaiting a more supportive custom powerchair. Now at 25, I am unable to sit, stand, or walk. My current wheelchair has braces along my ribs, elbows, thighs, and knees for lateral support. It also features straps and harnesses that prevent me from sliding or experiencing postural issues. This support is critical; without it, I would encounter serious difficulties maintaining a proper sitting position and even basic mobility. The absence of appropriate supports makes simple tasks impossible, like reaching out to grab my phone or using standard tables. Recently, I’ve been unable to hold my own head up, requiring a Headmaster Collar to keep my head from dropping. Breathing is a constant struggle that has intensified since I turned 23. My need for a BiPAP machine now averages 21-22 hours a day, and I experience severe discomfort after short intervals without it. My state deteriorates quickly into hypercapnia symptoms which disable my ability to stay awake after prolonged periods without support. Around May, I noticed a further decline in my physical strength, with a recognizable pattern of losing abilities that I then adjust to over time. Each drop in my baseline has been permanent; I have never regained a higher functionality after a decline. Factors like illness or mental health struggles seem to have a tangible impact on my condition. This May marked a difficult period during which I could not manage my hobbies or any concentration-demanding activities. I had to focus exclusively on improving my breathing, navigating each day with the constant awareness that my breaths were shallow. After several grueling weeks, I found a way to acquire a BiPAP. I have seen a remarkable improvement in my quality of life since getting it. I’m now able to manage tasks at home that fell by the wayside during my physical downturn. My medical team has acknowledged that my breathing mechanics appear compromised, as my diaphragm is significantly underutilized. My unassisted breaths are often rapid and insufficient, while breaths assisted by the BiPAP are deep and evenly distributed throughout my body. While I am not currently alarmed about my immediate future, the long-term trajectory appears concerning. I take precautions to avoid infections and stay vigilant about my health. I do realize the progression of my condition remains unyielded, and my history suggests increasing difficulty rather than stabilization. The reality is daunting; my loved ones are understandably anxious about my situation. While I maintain a sense of acceptance about my condition, I am acutely aware that my life trajectory is unlikely to include longevity without significant medical intervention. I fear not only my own deterioration but also the toll it takes on those I cherish. I deeply wish for the time and support to improve my quality of life while I’m still capable. To sum up, I've undergone various tests throughout the years, including a normal MRI of my brain and spine alongside other assessments that yielded inconclusive results. I have been advised repeatedly to pursue further testing to clarify my condition; however, accessibility in the public health system has hindered this. **Given your experience, I am curious: How long do patients with a progressive trajectory like mine typically survive? I can envision living into my 30s if I receive adequate healthcare and support, but is it realistic to think I could reach 40 or even 50?**