OpenHealth Q&A

Get answered by medical professionals

Tenderness in the Scalp and Temple

8/29/2025, 12:26:19 AMMale25-34

A 40-year-old female with a history of migraines has been experiencing intermittent discomfort in her right temple for the last few months. The pain fluctuates between sharp and dull sensations. Notably, during scalp massages, such as those provided at hair salons, she has observed that her right scalp is significantly more sensitive, regardless of whether she is currently feeling pain in her temple. She predominantly sleeps on her right side, as sleeping on her left tends to trigger Benign Paroxysmal Positional Vertigo (BPPV) in her left ear. The only possible explanation she can think of for her symptoms is temporal arthritis. While her ENT physician mentioned this as a possibility, they did not appear overly concerned. She wonders whether the pain should exhibit a consistent worsening pattern or if the intermittent nature of her symptoms could still be expected.

ArthritisMultiple SclerosisCrohn's Disease

Answers (1)

Cony

8/29/2025, 12:26:35 AM

OpenHealth AI

Experiencing tenderness in the scalp and intermittent discomfort in the right temple can understandably be concerning, especially with your history of migraines. While conditions like temporal arthritis can be a possibility, your symptoms can also result from various other factors, including tension headaches, muscle strain, or even migraine-related sensitivity.

Explanation

Your symptoms appear to fluctuate, which suggests a few possibilities:

  • Tension headaches: These can cause dull, aching pain and may increase sensitivity in the scalp.
  • Migraines: Given your history, migraines can manifest with both temple pain and tenderness in specific areas.
  • Muscle tension: If you’re sleeping predominantly on your right side, muscle strain could contribute to your discomfort.
  • Temporal arteritis: Although this can cause scalp tenderness as well, it typically presents with more persistent, severe symptoms and is associated with other systemic signs.

Next Steps

  1. Monitor Symptoms: Keep a diary of your pain intensity, duration, and any potential triggers (e.g., sleep position, stress). This can help identify patterns or changes.

  2. Adjust Sleep Position: Since sleeping on your right side seems to correlate with your discomfort, try to adjust your sleeping position gradually or use supportive pillows to relieve pressure on your scalp.

  3. Gentle Scalp Massage: Continue using gentle techniques when massaging your scalp. Avoid pressing too hard on tender areas until more clarity is gained about the cause.

  4. Stress Management: Incorporate relaxation techniques such as gentle yoga, meditation, or deep breathing exercises, which may reduce muscle tension and the frequency of headaches.

  5. Track for Changes: If you notice any new symptoms, such as worsening pain, visual changes, or other systemic symptoms (like fever or fatigue), keep a close eye and reassess the need for further evaluation.

Take care to stay hydrated and maintain a balanced diet, as these factors also contribute to overall headache management. If symptoms persist or worsen, additional investigation may become warranted to rule out concerns such as temporal arteritis or other neurological issues. Please take care of yourself and monitor your symptoms closely.

Related Questions

Seeking Clarity on Medical Notes

Greetings, I’ve chosen to use a throwaway account to keep my medical details private from my main one. My daughter, a 3-year-old with cerebral palsy, is prescribed baclofen, gabapentin, senna, and occasionally, Miralax. She is raised in a smoke-free and alcohol-free environment. Recently, my daughter has exhibited instances of staring and being unresponsive, which we discussed with her pediatric neurologist. These episodes occurred multiple times over three weeks. Concerned about potential seizure activity, we recorded some incidents and shared them with the doctor. He advised us to schedule an EEG, which was set for the soonest available time a week later, while instructing us to call if more episodes occurred. When another episode took place, we reached out to the neurologist, who practices at a children’s hospital approximately two hours away. He recommended that we go to our local emergency room. Upon arriving there, the attending physician reviewed her history but seemed skeptical. After a lengthy wait and attempts to clarify our situation, the on-call neurologist eventually came to see us—although he showed little interest in the video evidence we provided. He proceeded with an EEG that lasted only 15 minutes during which my daughter did not have any episodes. Unfortunately, this neurologist was rather abrupt and seemed dismissive, ultimately sending us home without satisfactory answers. Now, I find myself puzzled. In the EEG report, the neurologist mentioned something called a "teddy bear sign." As I had never encountered this term before, I did some research and discovered that it may suggest that seizure activity is not genuine if the patient is in possession of a stuffed animal or similar item. Is this a legitimate observation? My daughter indeed had her beloved baby doll, which she takes with her everywhere. I fail to comprehend how this could be relevant or why it might indicate that her potential seizure activity is fabricated. I plan to reach out to her primary neurologist to gain deeper insight into the meaning of this "teddy bear sign." Thank you for your help!

Multiple SclerosisLupusEndocrinology
Male25-34
6 minutes ago

Evaluating the Reliability of Blood Tests for Liver Disease

As a 30-year-old man who has indulged in heavy drinking during weekends for the past decade, I recently sought to understand the health of my liver through a blood test conducted at a laboratory. Initially, I felt a wave of relief when I received my results indicating that all my liver enzyme levels were within normal limits. However, my sense of security was short-lived as I stumbled upon information suggesting that some forms of liver disease might not be detectable through standard blood testing. This has prompted me to question the extent to which I can rely on my test results. Is it possible that underlying issues might still exist despite what the blood work revealed?

ArthritisCrohn's DiseaseInternal Medicine
Male25-34
6 minutes ago

Mysterious Health Decline

My uncle, a 64-year-old man, is experiencing a steep decline in health, yet the physicians he has consulted seem baffled by his condition. He neither smokes nor consumes alcohol, and the only medication I am certain he takes is Reglan. To provide some context, I am his niece, and he has been slightly overweight while living in a cluttered environment for as long as I can remember. I mention this because I wonder if the toxic surroundings might be a factor in his health issues. Although tests for heavy metals and ammonia showed no alarming results, he lived with an indoor cat and likely had other uninvited critters contributing to the toxicity of his home. For years, we’ve attempted to assist him in improving his situation, but he was resistant to our efforts. In September 2025, he underwent gallbladder removal surgery. Prior to this, he was capable of functioning independently. Unfortunately, post-surgery, he encountered severe nausea that prevented him from keeping food down, resulting in a loss of 60 pounds over three months. A doctor managed to stabilize him on Reglan enough for his appetite to return, but the lingering malnutrition had already inflicted significant harm. By early December, he was relocated to a rehabilitation section of a nursing home for temporary care while we sought a new living arrangement for him. Since that time, he has lost all mobility in his legs and his left arm. His right arm has limited functionality, leaving him unable to answer phone calls or feed himself. Additionally, symptoms of dementia have emerged, including hallucinations, confusion about close family members, episodes of unresponsiveness, and conversations with people who passed away decades ago. Although he does have sporadic moments of clarity, these instances are dwindling. After several days of mental distress, he becomes utterly drained, lacking the energy even for coherent conversation. He underwent an MRI early in this process, but it yielded no conclusive results. Additionally, he had a test that utilized electrically charged needles to assess the responsiveness of the muscles and nerves in his limbs, but these were unresponsive. Another MRI is scheduled for this week, yet the neurologist's recommendation of intensive physical therapy seems unrealistic given his current inability to move; even the physical therapist found humor in this suggestion. Guillain-Barre syndrome was proposed as a potential diagnosis, but no follow-up has occurred from his doctors regarding this possibility. Currently, he has been moved to a more permanent facility within the nursing home. His vital signs seem stable, and bodily functions appear otherwise normal, aside from the neurological concerns and his immobility. Residing in a small town limits access to specialists, but my father is trying to transfer him to a facility in Atlanta, possibly Mayo or Emory (I can't recall which specifically), for further evaluation, though his insurance is creating significant obstacles. While most of our family has resigned to the thought that he may not return to his previous state, I find it hard to accept that there isn’t at least one specialist out there who could provide insight into his condition, especially considering he was relatively normal just a year ago last August. Any thoughts or suggestions for additional testing would be greatly appreciated. Thank you for taking the time to read this lengthy message.

Multiple SclerosisLupusFibromyalgia
Male25-34
16 minutes ago

ENT Inquiry: Can Nasal or Sinus Cancer Develop in 3 Months Post-Normal Endoscopy?

Subject: 62 Years Old Gender: Female Background: Long-standing nasal and sinus issues My mother has grappled with persistent nasal blockages, sinus discomfort, and ear pressure for a considerable period. Approximately three months prior, she underwent a flexible fiberoptic nasal endoscopy, which revealed signs indicative of chronic rhinitis and sinusitis. The examination showcased features such as inflamed and discolored mucosa, enlarged nasal turbinates, and the presence of clear mucus. Importantly, no masses or concerning lesions were identified during this evaluation. Additionally, her oropharyngeal examination yielded normal results. However, during a recent ENT consultation, a “suspicious lesion above the middle turbinate” was identified via endoscopy, which prompted a referral for an “urgent” CT scan (scheduled for three weeks from now, as we reside in Croatia). Currently, she does not exhibit any worsening symptoms such as facial swelling, altered vision, or recurring nosebleeds (two notable nosebleeds occurred around a year ago, but she has not experienced any since then). I have a few inquiries: 1. Is it feasible for a malignant tumor in the nasal or sinus region to arise or become significant within a mere three months, given that a fiberoptic endoscopy conducted three months earlier revealed no alarming findings? 2. Considering this clinical scenario, how much more likely could this be a nasal polyp or chronic inflammatory reaction as opposed to a cancerous growth? 3. Is there a possibility that such a lesion existed three months prior but eluded detection during the fiberoptic endoscopy? I greatly appreciate any guidance you can provide regarding these concerns.

ArthritisCrohn's DiseaseInternal Medicine
Male25-34
26 minutes ago

In Need of Support

Greetings, I'm a 23-year-old male who actively participates in sports. It was around April that I started experiencing persistent pain in my shoulder and sacroiliac joint. By July, after taking finasteride for a period of three weeks, my joint discomfort intensified significantly and began affecting almost every joint in my body. Additionally, I noticed that my joints became unusually loose, leading to my shoulders partially dislocating from their sockets. This also brought on severe cognitive fog and a sensation of pressure in my head. I am losing my sense of optimism. If anyone has insights or assistance to offer, I would greatly appreciate it. To highlight, I have never had hypermobility nor have I been particularly flexible before this issue arose.

ArthritisMultiple SclerosisFibromyalgia
Male25-34
26 minutes ago