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  2. Dermatitis herpetiformis - Wikipedia

    en.wikipedia.org/wiki/Dermatitis_herpetiformis

    Dermatitis herpetiformis (DH) is a chronic autoimmune blistering skin condition, [3] characterised by intensely itchy blisters filled with a watery fluid. [4] DH is a cutaneous manifestation of coeliac disease , [ 5 ] although the exact causal mechanism is not known.

  3. Transient acantholytic dermatosis - Wikipedia

    en.wikipedia.org/wiki/Transient_acantholytic...

    One series of 300 patients with Grover's disease reported an association with other coexisting dermatoses including atopic dermatitis, contact dermatitis, and xerosis cutis. [6] More recent reports have indicated a connection with the Pfizer vaccine for Covid-19 [ 7 ] and as a presenting symptom of SARS-CoV-2 infection itself. [ 8 ]

  4. Dermatitis - Wikipedia

    en.wikipedia.org/wiki/Dermatitis

    Contact dermatitis is typically treated by avoiding the allergen or irritant. [9] [10] Antihistamines may help with sleep and decrease nighttime scratching. [2] Dermatitis was estimated to affect 245 million people globally in 2015, [6] or 3.34% of the world population. Atopic dermatitis is the most common type and generally starts in childhood.

  5. Keratosis pilaris - Wikipedia

    en.wikipedia.org/wiki/Keratosis_pilaris

    Keratosis pilaris (KP; also follicular keratosis, lichen pilaris, or colloquially chicken skin. [1]) is a common, autosomal-dominant, genetic condition of the skin's hair follicles characterized by the appearance of possibly itchy, small, gooseflesh-like bumps, with varying degrees of reddening or inflammation. [2]

  6. Dyshidrosis - Wikipedia

    en.wikipedia.org/wiki/Dyshidrosis

    Dyshidrosis is a type of dermatitis, characterized by itchy vesicles of 1–2 mm in size, on the palms of the hands, sides of fingers, or bottoms of the feet. [8] Outbreaks usually conclude within three to four weeks, but often recur.

  7. Linear IgA bullous dermatosis - Wikipedia

    en.wikipedia.org/wiki/Linear_IgA_bullous_dermatosis

    Adult linear IgA disease is an acquired, autoimmune blistering disease that may present with a clinical pattern of vesicles indistinguishable from dermatitis herpetiformis, or with vesicles and bullae in a bullous pemphigoid-like appearance. [2] This disease can often be difficult to treat even with usually effective medications such as ...

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