Welcome to I See AL amyloidosis, a dedicated resource to help healthcare practitioners find the latest information about the signs, symptoms and diagnosis of AL amyloidosis.
AL amyloidosis is a rare and fatal disease characterised by misfolded proteins that produce abnormal light chains. These chains may form amyloid fibrils, which aggregate and deposit in multiple vital organs.
AL amyloidosis is also clinically evident in soft tissues in 17% of cases.
AL amyloidosis impacts the lives of tens of thousands of patients each year. It is not easy to identify. Improved disease awareness is one of the critical components of achieving earlier diagnosis and improved prognosis.
Patients present with a range of symptoms. Proper diagnosis commonly takes ≥1 year after initial presentation.
One third of patients may visit ≥5 different physicians before diagnosis.
AL AMYLOIDOSIS IS A LIFE-THREATENING DISEASE, AND A DELAYED DIAGNOSIS IS DIRECTLY LINKED TO POORER OUTCOMES
Dr Vaishali Sanchorawala (haematology/oncology) and Dr Omar Siddiqi (cardiology) highlight the need to recognise the symptoms of AL amyloidosis early.
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A dedicated online resource for healthcare professionals to learn about the diagnosis and management of rare haematological malignancies: AL amyloidosis, Waldenström's macroglobulinemia, mantle cell lymphoma and acute myeloid leukaemia.