OpenHealth Q&A

Get answered by medical professionals

Chronic Aphthous Ulcers: Seeking Guidance

6/23/2025, 12:40:23 PMMale25-34

I’m reaching out for guidance regarding a young adult male who has been suffering from severe mouth and esophageal aphthous ulcers since childhood. These ulcers are plentiful and can grow to significant sizes (approximately 1 to 1.5 centimeters), leading to challenges in speaking and noticeable weight loss. He consistently develops these ulcers in conjunction with viral infections; it happens without fail. Notably, he experienced a very severe case of hand-foot-and-mouth disease, which significantly damaged the soft tissue inside his mouth, requiring pain management. We have consulted numerous physicians. During his childhood, a dermatologist suggested a dexamethasone rinse that provided marginal relief, although it proved ineffective for ulcers located in his esophagus. We have tried various remedies, including magic mouthwash and peroxyl. Recently, he underwent an upper gastrointestinal examination and a colonoscopy to eliminate the possibility of ulcers deeper in the gastrointestinal tract, and both tests returned normal results. For context, I have celiac disease, Sjögren's syndrome, and a history of colitis, but according to the doctor, he does not have Behçet’s disease. His case is further complicated by the fact that he is a college student who has transitioned from his pediatrician, who was not particularly helpful in this matter, to a new primary care provider, for whom he is currently on a waiting list. I have several inquiries: * Would it be advisable to perform a lip biopsy at this stage to confirm the presence of ulcers? * Which medical specialist is most suitable to address this issue? * Are there specific blood tests that could yield useful information? * Do you have any other recommendations or insights? I genuinely appreciate any assistance you might provide. He has been enduring this condition since he was a toddler and aspires to become a physician himself. Thank you for your invaluable feedback!

Multiple SclerosisLupusRheumatology

Answers (1)

Cony

6/23/2025, 12:40:45 PM

OpenHealth AI

Thank you for sharing the detailed context regarding this young man's struggles with severe aphthous ulcers. It's clear that his condition is causing significant distress and affecting his quality of life. Below are key considerations regarding his situation and recommendations to help manage his symptoms.

Key Points:

  1. Specialist Consultation: Consider consulting a specialist in oral medicine or a gastroenterologist with experience in managing mucosal disorders.
  2. Diagnostic Investigation: Blood tests may not be definitive, but certain tests could help rule out underlying conditions.
  3. Management Options: There are various treatment strategies that may help alleviate symptoms and manage outbreaks.

Explanation

Aphthous ulcers can be complex and are often linked to multiple triggers, including viral infections and potential underlying systemic conditions. Given the long history and the severity of the symptoms, a comprehensive approach is warranted to address both the current outbreaks and potential underlying issues.

Recommendations

  1. Consult a Specialist:

    • Consider seeing an oral medicine specialist or a gastroenterologist. They have expertise in managing oral and gastrointestinal mucosal issues and can provide tailored advice and potentially more advanced treatment options.
  2. Diagnostic Evaluation:

    • A lip biopsy may be useful if there's a suspicion of underlying lesions causing ulcers, but it’s typically reserved for more complex cases. Discuss with the specialist whether this could provide valuable insights.
    • Blood tests such as autoimmune panels can identify conditions like lupus or other autoimmune disorders that could be contributing to ulcer formation. This may include checking for vitamin deficiencies (like vitamin B12, folate, iron) or potential metabolic disorders.
  3. Management Strategies:

    • Topical Treatments: Since dexamethasone rinse provided limited improvement, alternatives could include stronger topical corticosteroids (e.g., clobetasol gel) or other agents like Aloe Vera gel or silver sulfadiazine.
    • Systemic Therapy: If ulcers are frequent and debilitating, systemic medications may be indicated. Options include:
      • Colchicine or other immunomodulators that may reduce the frequency of aphthous ulcers.
      • Oral corticosteroids in severe cases, but these come with potential side effects and should be carefully monitored.
    • Supportive Care: Focus on maintaining oral hygiene and soft foods to ease eating and minimize pain during outbreaks. Consider using a high-protein or liquid diet during flare-ups to address weight loss.
  4. Self-Care Suggestions:

    • Encourage him to keep a symptom diary to track triggers associated with outbreaks or changes in his health. This information can be invaluable for consultations with specialists.
    • Stress Management: Since stress can exacerbate ulcers, incorporating relaxation techniques such as mindfulness, yoga, or moderate exercise may help.

Feel free to reach out with further questions or clarifications, and I hope this young man finds relief soon as he pursues his aspirations in medicine.

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!

LupusThyroid DisordersEndocrinology
Male25-34
54 minutes ago

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.

Multiple SclerosisCrohn's DiseaseEndocrinology
Male25-34
1 hour ago

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.

ArthritisCOPDRheumatology
Male25-34
2 hours ago

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!

Thyroid DisordersEndocrinologyRheumatology
Male25-34
3 hours ago

28-Year-Old Male Experiencing Scalp Sensations Post-Amitriptyline Treatment

I am a 28-year-old man in generally good health, without any cardiac concerns. Approximately a month ago, I encountered intense pain localized to one side of my head, which was unresponsive to paracetamol. However, a single dose of a migraine treatment provided substantial relief. Following that, I began a regimen of amitriptyline, starting at a nightly dose of 10 to 25 mg. While my head pain has diminished significantly—by about 90 to 95%—I now experience occasional uncomfortable sensations on my scalp. These feelings include pins and needles, a cooling sensation, and some crawling feelings near my hairline and ears. There are fleeting moments where I feel brief throbs lasting a second, but I do not have any persistent headaches. To clarify, I do not experience any of the following: - Nausea - Weakness in my limbs - Numbness - Changes in my vision - Coordination difficulties - Seizures The symptoms I have are transient, shifting around and often intensifying when I become conscious of them or as the day progresses. I would like to know: Is it common to experience these sensations during the recovery stage following episodes of neuralgia or migraine-like discomfort? Additionally, could the amitriptyline potentially be causing these temporary paresthetic sensations? I am seeking some reassurance or advice on what is typically observed during this healing process. Thank you.

Multiple SclerosisCrohn's DiseaseEndocrinology
Male25-34
4 hours ago