aldara and vitiligo

albinism of the ocular type, autoimmune polyendocrinopathy syndrome, congenital deafness with vitilego and achalasia, dyschromatosis symmetrica hereditaria, ermine phenotype, familial histiocyctic reticulosis, kabuki syndrome, and the syndrome of spastic paraparesis, vitiligo, premature graying and characteristic facies.

Autoimmune diseases occur when these reactions inexplicably take place against the body own cells and tissue by producing self-reactive antibodies. In vitiligo, the autoantibody is directed against the melanocytes. http://www.aarda.org/patient_information.

My primary care physician did test my thyroid when I first met him when he noticed I had Vitiligo and I found out I have hypothyroidism. I am being treated for that but I've read that this autoimmune disorder may be caused by vitamin deficiencies and my doctor has never mentioned I should be tested.

The doctor called it vulvar dysplasia, and he prescribed aldara cream 3 times a week because he said that since there are so many a laser would be very painful and that we should try to remove some with aldara first. I have a few questions about using aldara. 1) is it harmful to shave on off days from using aldara? 2) Can shaving make the warts worse? 3) Is sex okay when the cream is not on the skin? Thank you!

Yes, I'm not saying that Aldara acts on HPV itself. It is indeed the body's own immune system that gets rid of HPV-infected cells, however since the virus is not systemic and lays on the outskirts of your skin, it is hard for the immune cells to detect it and excrete cytotoxins that destroy compromised cells. That's why Aldara is marketed as "killing HPV from the inside out".

s activity is, at least in part, correlated with the reaction that it generates. If you have been using Aldara for 4 weeks with no effect and little local reaction, it is time to try something else such as freezing with liquid nitrogen. In answer to your specific questions however: 1. No, the location has little to do with response. Warts that have appeared more recently tend to respond better.

To have a second opinion we went to an another dermatologist he said it is not vitiligo and is 100 % curable this may be because of thyroid / liver problem and suggested LFT and thyroid tests. Now am totally confused what to do, what all tests (another than the mentioned above) should we do so as to know the actual cause. Is there any tests / specific symptoms for vitiligo ?

I just found out I had HPV yesterday and had my warts frozen and was given aldara to use in two days time. My question was, when would it be ok to masturbate again, and when would it be ok to have sex again?

White spots on the body may suggest a fungal infection, pityriasis alba, and vitiligo. Vitiligo presents as white patches which may occur symmetrically in both sides of the body. The borders are well demarcated. As for fungal infections, it presents as white patches of skin with a central scaling. It may not be stark white unlike vitiligo. Pityriasis usually involves children.They present as diffuse patches of whitish spots. I suggest you have this assessed by your dermatologist.

Update: Yes, there is a relationship. I now have both vitiligo and alopecia areata. The doctors have confirmed that there is a relationship as well as the alopecia areata registry. In case anyone has the same question...now you know :) Thanks! This discussion is related to <a href="/posts/Autoimmune-Disorders/Relationship-btw-Alopecia-areata-and-Vitiligo/show/1456377">Relationship btw Alopecia areata and Vitiligo?</a>.

First I noticed vitiligo on my inner wrists and a small amount near my mouth. Then a year later was diagnosed as hypothyroid. Next, I seem to not have the general health I used to -- find I'm much more susceptible to viruses, etc., even ending up with shingles at one point. Seems like my immune system is failing me in several areas. Anyone else with Hashimoto's experiencing this same pattern? Any suggestions to halt or slow down this decline?

White skin patches may have fungal infections, pityriasis alba and vitiligo as differentials. These are differentials that you may need to consider for any hypopigmented areas on the skin. Is there any scaling involved?

m a 48 year old female and have developed flat brown splotchy hyperpigmentation on my face and arms. What is this? Is it hormonal? How do I get rid of it and prevent more? I also have areas of depigmentation (small white spots) all over my arms and legs. Again, what is it and can I get rid of it and prevent more? I'd appreciate any information about causes and potential treatment options. Thank you.

19 year old male began having depigmentation around eyes, mouth, side of torso, full thumbs, and on finger tips at 18 years old. Dermatologist and GP think vitiligo but no visible improvement from prednizone 50 mg, betamethasone dipropionate .05% topical, elidel pimecromlimus cream 1%. Biopsy of skin on finger stated “a normal density of epidermal melanocyte which argues against vitiligo. No fungal, organism or increased much were found.

I did drastically change my diet though eating more vegetables and fruits and taking a daily vitamin and reducing alcohol intake and not smoking at all. I will continue using aldara and hopefully *fingers crossed* all the warts will go away :) im very thankful and hope i dont need surgery which the date was already set for. so for all of you that are in the same boat as i am in I would strongly recommend taking aldara its worth a try!

I used aldara with great success. However, I have read it has a higher success rate in females than males. Still, I do not know how credible this information exactly is. I found using Aldara to clear up the majority of warts, and then using a different treatment (such as cryo) to clear any remaining warts seemed to be effective. I used a combination of TCA and Aldara, and have been wart free for a month now (took 3 months to entirely clear).

i would stop the use and the redness/ swelling would go away and i would contine use and everything would be okay. recently i bought an aldara imitation cream, not the same brand name as aldara and have been experiencing more of a rash like reddish irritation where i use the cream. when i stop using it it will almost go away totaly but when i start back up using the cream the same rash in the same place will re appear. so im not sure if its the cheaper cream or if i have herpes.

I've been using Aldara for over two weeks now and am experiencing absolutely no side effects at all. Now I'm not disappointed believe me, but the one and only nice thing about side effects is that they indicate that whatever you are using is not "working" per-se but that it's doing *something*. Is this normal? Also, my doctor did a pretty deep freeze of the warts before sending me home with Aldara.

Current treatment options for vitiligo include medical - topical steroid therapy , oral and topical psoralen photochemotherapy and depigmentation using hydroquinone; surgical-autologous skin grafts and micropigmentation, and adjunctive therapies- sunscreens and cosmetic products.' You can get a thyroid function test done if you feel it is required in consultation with your doctor. You could read more about this condition at the following links - http://www.medicinenet.

I have recently been using Aldara cream to try and eliminate my genital warts (HPV). Although the warts minimised in size after three months my doctor told me to stop using aldara because of the ineffectiveness and incredible sores and lesions that i endured whilst treatment. He reccomended me to a dermatologist for the treatment of the HPV.

I was just diagnosed with genital warts, probably the worst news i had ever heard only because the amount of partners I had been with was very slim and my fiance is the only person that I did not use a condom with....anyways, i have several questions that keep running through my head and need some answers to hold me over till i talk to my doctors next. Once my outbreak goes away with the medicine my doctor prescribed me (Aldara) will they keep coming back monthly?

while your boyfriend probably didn't get HPV from kissing you, he could have gotten the Epstein Barr Virus, which explains the sore throat. The Epstein Barr Virus is a very serious virus although doctors typically don't want to scare you and tell you this. It causes a really bad cancer...lymphoma!!! (i.e. Hodgkin's disease possibly). It doesn't absolutely cause this, but you have a VERY increased risk of developing lymphoma once you get the Epstein Barr Virus.

The pressure urticaria and vitiligo is what made me think thyroid. I had the rheumatoid factor and that was negative. That's when we discovered the low positive ANA. Thanks so much!! O and my mom has rheumatoid, fibro, lichen planus, and ulcerative colitis What type of test would you run for the symptoms I mentioned?

Aldara and vitiligo

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