cure for erythema multiforme?

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It is generally thought to be an allergic reaction (hypersensitivity), and milder forms of the "rash" goes away pretty quickly. If you can treat the underlying cause of the reaction then you can control it. Medications, foods and other things may cause the reaction.

There can be extensive involvement, and some may be triggered by herpes virus. In these cases the treatment may be more diffcult. In cases caused by herpes an antiviral medication may help. In very serious cases skin grafts might even be called for.  (+ info)

I took my 3 year old son to the ER . He has a rash all over and a fever they said its Erythema Multiforme?

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he was taking an antibiotic this is why he got this has anyone ever had this ? or know someone who has ? I'm taking him to the doc in the AM just wonder what i should ask

Thanks for any and all help
Erythema multiforme is a common rash, the name just means it is redness (the erythema part), multiforme (because it takes on varied appearance). It's usually viral in origin, but it is also associated with medications. In his case, it may be due to the antibiotic, or another virus has simply taken advantage of the situation where his immune system is already busy elsewhere. It's unusual in a child of his age, but not entirely unheard of. I'd wait to see what the pediatrician has to say about it. You may be in for a change of antibiotic at the very least. If it is a true EM rash, it will last about 2 weeks, no matter what you do, as that's the usual time frame to battle off a virus. In the meantime he'll be more comfy after a cool bath with a handful of oatmeal thrown in, or a handful of baking soda. Also strip him to the shorts, and keep him fairly cool and out of sunlight. If he gets in the least bit sweaty or hot he'll itch and be in misery. He needs lots to drink, and whatever you can get him to eat is fine. It's not usually contagious, so if there are other children you probably have no worries there. Keep the fever in control with children's Tylenol or Ibuprofen. When the fever comes down, he'll probably feel like being up and messing about- it's amazing how resilient they are. Otherwise, just wait to see what the pediatrician has to say about it all. He should do fine, just itchy and red until it finally goes it's way. I've had 6, with plenty of mystery rashes along the way, and seen plenty more through work. Most go as quietly as they came on, with no problems aside from living with the itchy, grumpy child in the meantime.  (+ info)

What is diffuse erythema plus and diffuse gastritis?

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I have an endoscopy result with following results
diffuse erythema+ and final impression says diffuse gastritis.
Can anybody explain what does they mean?
Diffuse means scattered and erythema is redness. Gastritis is inflammation of the stomach lining. You have redness and inflammation in your stomach, spread around rather than in just one place. With this result your doctor should be able to prescribe medicine to help.  (+ info)

what to do to mild erythema in the lower eosophagus and mild erosion to the first part of deodenum?

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i had a previous treatment for the H.pylori.Now i am suffering from a pain in my stomach.The doctor saw a mild erythema in my lower esophagus and mild erosion in the duodenum.I did not take the biopsy. His impression is gastroduodenitis.the question is ;What is the treatment and diet that should be taken?
Gastro- duodenoscopy might have been done to detect erythema of lowerpart of the esophagus and duodenum.This may be due persistance or relapse of H.Pylori infection.Omeperazole group of drugs
with or without antibiotic supplementation will help you. Please consult Gastroenterologist for the definitive type of treatment. No special dietary precautions are necessary. Avoid spicy and hot(for taste)foods.  (+ info)

What are some treatments for severe Idiopathic craniofacial erythema?

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I think i have severe Idiopathic craniofacial erythema because my face goes red whenever someone even says my name. School it is most common and im getting tired of being scared to go to school fearing by face will turn red and it gets worse when everyone notices. I feel like im on fire and then i can't concentrate on school work, or ask questions or comment so my face goes red so i dont get very good "participation" marks. Please help me.
According to experiencefestival.com, "A number of treatments are available. The most successful non-invasive procedure is cognitive behavioural therapy (CBT), which attempts to alleviate the anxiety felt by sufferers.

"In extreme cases a surgical procedure known as Endoscopic Transthoracic Sympathicotomy (ETS) is available. Pioneered by surgeons in Sweden, this procedure has recently become increasingly controversial due to its many potential adverse effects. Patients who have undergone the procedure frequently complain of compensatory sweating and fatigue. ETS is now normally only considered in extreme cases where other treatments have been ineffective."

I checked out Wikipedia.org for the definition of Endoscopic Transthoracic Sympathicotomy, and it says that, "Endoscopic thoracic sympathectomy (ETS) is a surgical procedure where certain portions of the sympathetic nerve trunk are destroyed. ETS is used to treat hyperhidrosis, facial blushing, Raynaud's disease and Reflex Sympathetic Dystrophy. By far the most common complaint treated with ETS is palmar hyperhidrosis, or "sweaty palms". In this disorder, the palms may constantly shed so much sweat that the affected person is unable to handle paper, sign documents, keep clothes dry, or shake hands. The result is often social phobia so severe as to be disabling.

Sympathectomy refers to the destruction of tissue anywhere in either of the two sympathetic trunks, long chains of nerve ganglia lying along either side of the spine. Each trunk is broadly divided into three regions: cervical (up by the neck), thoracic (in the chest) and lumbar (in the lower back). The most common area targeted in sympathectomy is the upper thoracic region, that part of the sympathetic chain lying between the first and fifth thoracic vertebrae."

I hope you find something that will bring you the relief I'm sure you're desperate for.  (+ info)

Can Lexa pro be taken by a person with glioblastoma multiforme brain cancer?

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A friend who has glioblastoma multiforme brain cancer was recently prescribed lexapro for depression & anxiety. Since taking for only 4 days it seems to have caused lack of appetite, aggression, short temper, further depression. Is this worth it, we are told that it could take 4-8 weeks to work and I have been reading about the side effects...anyone who is familiar with this?
Obviously your doctor thought it was worth it to prescribe it to you. Any other similar drug will take just as long to work and most the side effects will become less or go away as time passes.  (+ info)

What color is the ribbon for glioblastoma multiforme?

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I know that they have ribbons for other cancers and diseases, but what is the color for this one. My grandma just died from it, and i would just like to know. Thank you.
Glioblastoma Multiforme doesn't have its own ribbon, since it is such a specific diagnosis. My 3 year old son Conrad has medulloblastoma (another type of brain cancer) and the ribbon for brain cancer is gray. We are sorry for your loss. Brain cancer is a scary disease.
-Mommy to Super Conrad, 3yo brain cancer smasher!  (+ info)

How did she end up with Gliobastoma Multiforme?

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My best friend who is only 15 was diagnosed with stage four brain cancer (GBM). We were doing some research and they said it was most likely found in men, and men that were over 50. She's a 15 year old girl. I was wondering why she may have gotten this when its more likely for an older man? It is something herditary?

PS please pray for her shes on chemo and has been given 6 months to live. but i want her to see her 16th birthday in december.
Tell her any decent doctor would not give her a death sentence like 6 months to live. A good doctor never gives up. Also suggest she look into Avastin...it's newly approved for gbms. My gbm is also grade 4 and I'm 23. There's no research for people her age or my age...or very few studies. It is most common in men and senior citizens (over the age of 70), but it can effect everyone. It is not a hereditery cancer or tumor. I went through surgery, then 6 1/2 weeks of radiation (which both did great reduction to my tumor) then a year of temodar (oral chemo) which didn't work for me, but does great for most people, now I am on Avastin and an IV chemo which has been working well so far :) The sad part is that gbms are infamous for coming back over and over...most likely this is something she will fight forever. I was told after it's gone I've got about 5 to 6 years until I can expect to see a new one. My first isn't even gone and I've already had a 2nd and gotten rid of the 2nd. I was diagnosed in Dec 08. Best of luck to your friend. She will be in my thoughts. <3  (+ info)

Can anyone tell me what to expect when someone dies from a Glioblastoma Multiforme?

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My mom was diagnosed about 4 months ago with an inoperable Glioblastoma in her frontal lobe. Is there anyone out there that has witnessed this? My sister and I are taking care of her but we are not sure how fast she will pass, and what to expect. She finished traditional radiation about 6 weeks ago. And is taking maintenence Temodar. She is walking around now, but not talking a lot. And she has a lot of swelling due to high doses of steriods.
I'm sorry to hear about your Mom. I can't answer your question, but just wanted you to know I'll keep all of you in my prayers.  (+ info)

Anyone ever heard of someone or are you surviving a Glioblastoma Multiforme?

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I am a true believer of miracles, and I was just curious as to whether or not there have been any survivors that anyone knows about or if you are one I would like to hear from you!!
God Bless!!
No significant advancements in the treatment of glioblastoma have occurred in the past 25 years. Although current therapies remain palliative, they have been shown to prolong quality survival. Mean survival is inversely correlated with age, which may reflect exclusion of older patients from clinical trials. Without therapy, patients with GBMs uniformly die within 3 months. Patients treated with optimal therapy, including surgical resection, radiation therapy, and chemotherapy, have a median survival of approximately 12 months, with fewer than 25% of patients surviving up to 2 years and fewer than 10% of patients surviving up to 5 years. Whether the prognosis of patients with secondary glioblastoma is better than or similar to those patients with primary glioblastoma remains controversial,....That's what the doctors say, but i've heard of many people being cured from many things as worse as this thanks to the help and to the faith in their religion, in god. I believe that if you are a true believer u will overcome anything. Goodluck and many god bless.  (+ info)

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