Theresa Fogaren, Anthony C Shelton, Douglas V Faller, Dawn Marie Stull, Sara Thuenemann, Lisa Mendelson
BACKGROUND: Primary systemic light-chain (AL) amyloidosis is a rare clonal plasma cell disorder characterized by the production of abnormal immunoglobulin fragments, which form insoluble fibrils that aggregate as amyloid deposits in organs and tissues, leading to organ dysfunction and death. OBJECTIVES: The aim of this literature review is to increase awareness of AL amyloidosis and educate nurses on the care of this patient population. METHODS: This overview is based on a literature search of AL amyloidosis, including its pathogenesis, prognosis, and presentation...
July 25, 2022: Clinical Journal of Oncology Nursing