Dermatitis herpetiforme en joven con enfermedad celiaca silente. Virtual Soc. ISSN Dermatitis herpetiformis, also called Duhring-Brocq disease, is a recurrent disease characterized by symmetric chronic papulo-vesicular eruption, mainly located in extension surfaces, and intense pruritus. It is associated with a gluten-sensitive enteropathy. Its diagnosis is based on clinics, pathological anatomy and direct immunofluorescence apart from serological tests.
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Patients should address specific medical concerns with their physicians. Toggle navigation. VesiculoBullous Disorders Chapter. From Related Chapters. Page Contents Epidemiology Incidence : Up to 39 cases per , Usual onset at 20 to 40 years Gender preponderance in men by ratio Ethnicity Most commonly affects white patients Rarely affects black or asian patients. Symptoms: Precede lesion onset by 8 to 12 hours Intense Pruritus Skin burning. Signs Grouping of lesions may occur herpetiform-like Altered pigmentation at sites of healed lesions Polymorphous collection of lesions Urticaria l wheals Vesicle s Bulla e Erythematous Papule s Symmetric distribution of lesions on limbs and trunk Common sites Elbow s and knees Buttocks and Shoulder s Sacral area Uncommon sites Scalp and hairline Face and posterior neck Rare sites Palms and soles Mucus Membranes.
Differential Diagnosis Pemphigus hermetiformis. Course Prolonged course over years Spontaneous remission in one third of patients. Images: Related links to external sites from Bing. Related Studies. Trip Database TrendMD. Ontology: Dermatitis Herpetiformis C Definition NCI A chronic autoimmune skin disorder characterized by the development of pruritic papulovesicular and bullous lesions in the elbows, knees, buttocks, and back.
Definition MSH Rare, chronic, papulo-vesicular disease characterized by an intensely pruritic eruption consisting of various combinations of symmetrical, erythematous, papular, vesicular, or bullous lesions. A variety of different autoantibodies has been detected in small numbers in patients with dermatitis herpetiformis.
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A chronic autoimmune skin disorder characterized by the development of pruritic papulovesicular and bullous lesions in the elbows, knees, buttocks, and back. Rare, chronic, papulo-vesicular disease characterized by an intensely pruritic eruption consisting of various combinations of symmetrical, erythematous, papular, vesicular, or bullous lesions.
Disease or Syndrome T Morbo di Duhring , Dermatite erpetiforme. Dermatitis herpetiformis , Duhrings sykdom.
This table lists symptoms that people with this disease may have. For most diseases, symptoms will vary from person to person. People with the same disease may not have all the symptoms listed. The HPO collects information on symptoms that have been described in medical resources. The HPO is updated regularly. If you need medical advice, you can look for doctors or other healthcare professionals who have experience with this disease.
Was a pleasure to read Dr. Lesions usually begin with itching or burning sensation and erythematous papules or urticarial plaques. Grouped vesicles with centrifugal growth, with serous or hemorrhagic contents and symmetrical distribution were typical. Exulcerated skin and crusts were also seen, followed by residual hypo or hyperpigmentation. Even though, all the 14 patients were referred to Gastroenterology, only 6 of them pursue the specialist evaluation.
Dermatitis herpetiformis DH is a chronic autoimmune blistering skin condition,  characterised by blisters filled with a watery fluid  that is intensely itchy. DH is a cutaneous manifestation of Coeliac disease. Dermatitis herpetiformis was first described by Louis Adolphus Duhring in The age of onset is usually about 15—40, but DH also may affect children and the elderly. Men are slightly more affected than women. Dermatitis herpetiformis is characterized by intensely itchy , chronic papulovesicular eruptions, usually distributed symmetrically on extensor surfaces buttocks, back of neck, scalp, elbows, knees, back, hairline, groin, or face.