Abstract
Lymph node and spleen involvement is frequent in systemic amyloidosis. AL amyloidosis is the most common and clinically most important cause of lymph node amyloidosis. In most cases, the lymph node AL amyloidosis is systemic and caused by an underlying systemic plasma cell or B-cell neoplasm. For this reason, immunophenotypic analysis of the lymphoid component is required in these cases for management decisions. Other etiologies of lymph node amyloidosis include AA amyloidosis and rarely hereditary amyloidoses such as AAPOA1 or ATTR amyloidosis. By imaging studies, the spleen is involved in most cases of systemic AL and AA amyloidosis. Clinically splenic involvement may lead to hyposplenism, and occasionally, splenic rupture. In addition to AL and AA, amyloidosis and other systemic amyloidoses such as ALECT2 amyloidosis can also affect the spleen.
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Sen, F., Dogan, A. (2015). Amyloidosis of the Lymph Nodes and the Spleen. In: Picken, M., Herrera, G., Dogan, A. (eds) Amyloid and Related Disorders. Current Clinical Pathology. Humana Press, Cham. https://doi.org/10.1007/978-3-319-19294-9_32
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DOI: https://doi.org/10.1007/978-3-319-19294-9_32
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