Secondary systemic amyloidosis

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Secondary Systemic Amyloidosis

Secondary systemic amyloidosis (pronunciation: /ˌsɛkənˈdɛri sɪˌstɛmɪk ˌæmɪˈlɔɪˈdoʊsɪs/) is a form of amyloidosis that is typically associated with chronic inflammatory conditions.

Etymology

The term "secondary systemic amyloidosis" is derived from the Greek words "amyloid" meaning "starch-like" and "osis" meaning "condition". The prefix "secondary" is used to denote that the condition is a result of another underlying disease or condition.

Definition

Secondary systemic amyloidosis is a disorder characterized by the deposition of insoluble protein aggregates, known as amyloid fibrils, in various organs and tissues of the body. This condition is considered secondary because it often occurs as a complication of another disease that causes prolonged inflammation, such as rheumatoid arthritis, inflammatory bowel disease, or tuberculosis.

Symptoms

The symptoms of secondary systemic amyloidosis can vary widely depending on the organs affected. Common symptoms may include fatigue, weight loss, and swelling in the legs and ankles due to kidney disease. If the heart is affected, symptoms may include shortness of breath, irregular heartbeat, and fluid retention.

Diagnosis

Diagnosis of secondary systemic amyloidosis typically involves a combination of physical examination, medical history, and laboratory tests. A definitive diagnosis is usually made through a biopsy of affected tissue, which is then examined under a microscope for the presence of amyloid deposits.

Treatment

Treatment for secondary systemic amyloidosis primarily focuses on managing the underlying disease causing the inflammation. This may involve the use of anti-inflammatory medications, immune system suppressants, or other treatments specific to the underlying condition. In some cases, chemotherapy or stem cell transplantation may be used to slow the progression of the disease.

Related Terms

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