Secondary cutaneous amyloidosis

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Secondary Cutaneous Amyloidosis

Secondary cutaneous amyloidosis (pronunciation: sek-un-dair-ee kyoo-tay-nee-uhs am-uh-loi-doh-sis) is a type of amyloidosis that affects the skin. It is characterized by the deposition of amyloid proteins in the skin as a result of another disease or condition.

Etymology

The term "secondary cutaneous amyloidosis" is derived from the Latin "secundarius" meaning "second", the Greek "kutanea" meaning "skin", and the Greek "amyloid" meaning "starch-like", referring to the protein deposits that resemble starch when stained with iodine.

Definition

Secondary cutaneous amyloidosis is a condition where amyloid proteins are deposited in the skin as a secondary effect of another disease or condition. This is in contrast to primary cutaneous amyloidosis, where the amyloid deposits occur without a known cause or underlying condition.

Symptoms

Symptoms of secondary cutaneous amyloidosis can vary depending on the underlying condition causing the amyloid deposits. Common symptoms include skin changes such as rashes, nodules, or blisters, and systemic symptoms related to the underlying condition.

Causes

Secondary cutaneous amyloidosis is caused by an underlying disease or condition that leads to the abnormal production or accumulation of amyloid proteins. These conditions can include chronic inflammatory diseases, infections, and certain types of cancer.

Diagnosis

Diagnosis of secondary cutaneous amyloidosis typically involves a skin biopsy to confirm the presence of amyloid deposits. Additional testing may be required to identify the underlying condition causing the amyloidosis.

Treatment

Treatment for secondary cutaneous amyloidosis focuses on managing the underlying condition causing the amyloid deposits. This can involve medication, surgery, or other treatments depending on the specific condition.

Related Terms

External links

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