AI Article Synopsis

  • * About 10-15% of individuals with amyloidosis also develop multiple myeloma, but limited research has focused on the clinical and genetic characteristics of these patients.
  • * In this study, a patient with MM exhibited a complex near tetraploid karyotype with notable genetic abnormalities, particularly the t(11;14) translocation, which is commonly found in both MM and AL amyloidosis.

Article Abstract

Cytogenetic and iFISH plays a major part in the diagnosis of the MM and have an important prognostic significance. 10-15% of patients with amyloidosis will also have multiple myeloma (MM). Few studies have addressed the clinical and cytogenetic features of patients with AL amyloidosis with concurrent multiple myeloma. This study of MM case in which we found a near tetraploid complex karyotype with the t(11;14) (q13;q32) abnormality in cytogenetic analysis and the presence of t(4;14) and del(17p) by iFISH, referred to several studies which showed the translocation t(11;14) as the most frequent abnormality in both AL amyloidosis and MM.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7390876PMC
http://dx.doi.org/10.1016/j.lrr.2020.100217DOI Listing

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