Secondary cutaneous amyloidosis
Secondary cutaneous amyloidosis is a subtype of amyloidosis that is characterized by the deposition of amyloid proteins in the skin as a result of another disease or condition. This type of amyloidosis is different from primary cutaneous amyloidosis, which is not associated with any other diseases.
Causes[edit | edit source]
Secondary cutaneous amyloidosis is usually associated with chronic inflammatory skin diseases, such as lichen planus, bullous pemphigoid, and chronic ulcers. The exact mechanism of amyloid deposition in the skin is not fully understood, but it is believed to be related to the chronic inflammation and tissue damage caused by these diseases.
Symptoms[edit | edit source]
The symptoms of secondary cutaneous amyloidosis can vary depending on the underlying disease. However, common symptoms include skin lesions that are often itchy and can range in color from red to brown. These lesions can appear anywhere on the body, but are most commonly found on the legs, arms, and trunk.
Diagnosis[edit | edit source]
The diagnosis of secondary cutaneous amyloidosis is typically made through a skin biopsy, which involves removing a small sample of skin for examination under a microscope. The presence of amyloid proteins in the skin can be confirmed through special staining techniques.
Treatment[edit | edit source]
The treatment of secondary cutaneous amyloidosis primarily involves managing the underlying disease. This can include the use of medications to reduce inflammation and slow the progression of the disease. In some cases, surgery may be necessary to remove large deposits of amyloid proteins.
See also[edit | edit source]
Secondary cutaneous amyloidosis Resources | ||
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Contributors: Prab R. Tumpati, MD