{"id":11059,"date":"2025-07-27T13:58:07","date_gmt":"2025-07-27T11:58:07","guid":{"rendered":"https:\/\/valintermed.com\/?p=11059"},"modified":"2025-07-27T13:58:07","modified_gmt":"2025-07-27T11:58:07","slug":"priobretennyy-bulleznyy-epidermoliz","status":"publish","type":"post","link":"https:\/\/valintermed.com\/en\/medlibrary\/acquired-bullous-epidermal-necrosis\/","title":{"rendered":"Acquired epidermolysis bullosa"},"content":{"rendered":"
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Acquired epidermolysis bullosa (EB) is a rare skin disease characterized by the formation of blisters on the skin and mucous membranes that occur in response to mechanical trauma or other damage. EB is caused by a violation of the mechanical properties of the dermal and epidermal layers, which leads to weakness of the connections between them. Unlike hereditary epidermolysis bullosa, which is associated with genetic mutations, the acquired variant can be associated with various systemic diseases, infections and environmental factors. EB can have a severe course, especially in older people or with concomitant diseases, which requires careful diagnosis and targeted treatment.<\/p>\n

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