Treatment of Amyloidosis

Treatment for amyloidosis depends on the form of the disease, but goals generally include slowing its progression, reducing symptoms, and extending life. Treatments may include:

  • Chemotherapy: Chemotherapy medicines are often given intravenously (IV), subcutaneously, or orally. Common chemotherapy medicines for AL amyloidosis include bortezomib (Velcade), cyclophosphamide, and dexamethasone.
  • Stem cell transplantation: Autologous hematopoietic stem cell transplantation is considered the most effective treatment for amyloidosis in eligible patients.
  • Treating the underlying condition: For secondary amyloidosis (AA), the underlying condition must be treated. For example, eradication of infections can resolve AA lidoses.
  • Medications to help with symptoms: These include painkillers, anti-sickness medicines, and diuretics.
  • Kidney dialysis: If your kidneys are not working properly, you may need kidney dialysis.
  • Kidney transplant or liver transplant: If these organs are damaged, you may need a kidney transplant or liver transplant.
  • Supportive therapies: Treatments such as diuretics to manage fluid retention, blood thinners to reduce the risk of blood clots, and pain medications may be used to alleviate symptoms and improve quality of life.

Amyloidosis

Amyloidosis is a rare disease characterized by the abnormal accumulation of amyloid proteins in organs and tissues. This buildup can disrupt normal function and lead to organ damage. Amyloidosis symptoms may include weight loss, swelling, and organ dysfunction.

Amyloidosis treatment helps to manage symptoms, slow the progression of the disease, and address underlying conditions that may contribute to amyloidosis. In this article, we will study the meaning of amyloidosis, its types, stages of development, causes, symptoms, and treatment in detail.

Amyloidosis

Table of Content

  • Amyloidosis Meaning
  • Types of Amyloidosis
  • Stages of amyloidosis
  • Causes of Amyloidosis
  • Symptoms of Amyloidosis
  • Diagnosis of Amyloidosis
  • Treatment of Amyloidosis
  • Conclusion: Amyloidosis
  • FAQs on Amyloidosis

Similar Reads

Amyloidosis Meaning

Amyloidosis is a rare disease that occurs when abnormal proteins, called amyloid fibrils, build up in tissue throughout the body. These deposits can affect one organ or multiple and can build up in the heart, brain, kidneys, spleen, and other parts. Amyloidosis can be primary (due to abnormal production of amyloid proteins) or secondary (resulting from chronic inflammatory conditions or other diseases). In advanced stages, amyloidosis can lead to organ dysfunction and failure, highlighting the importance of early detection and management of this condition....

Types of Amyloidosis

The types of amyloidosis are:...

Stages of Amyloidosis

The stages of amyloidosis are:...

Causes of Amyloidosis

Causes of amyloidosis includes:...

Symptoms of Amyloidosis

Symptoms of Amyloidosis includes:...

Diagnosis of Amyloidosis

The diagnostic methods for amyloidosis are:...

Treatment of Amyloidosis

Treatment for amyloidosis depends on the form of the disease, but goals generally include slowing its progression, reducing symptoms, and extending life. Treatments may include:...

Conclusion – Amyloidosis

Amyloidosis is a rare, serious disease that can be difficult to diagnose because of its varied presentation. It’s caused by the accumulation of misfolded protein aggregates in the body’s tissues, which can lead to organ dysfunction, disability, and death. Amyloidosis can affect multiple organs and has different manifestations. Diagnosis involves a combination of medical history, imaging tests, and tissue biopsy. Treatment strategies aim to reduce the production of abnormal proteins, manage symptoms, and address complications through medications, chemotherapy, stem cell transplants, and supportive therapies....

FAQs on Amyloidosis

What are the Main Causes of Amyloidosis?...

Contact Us