Immunoglobulin heavy chain gene rearrangement in heavy chain deposition disease suggests it is a plasma cell disease: a case report

J Int Med Res. 2022 Mar;50(3):3000605221086428. doi: 10.1177/03000605221086428.

Abstract

Heavy chain deposition disease (HCDD) is characterized by the deposition of truncated monoclonal immunoglobulin heavy chains along glomerular basement membranes. Truncated heavy chains are thought to be associated with plasma cell disease (PCD), but previous bone marrow cytology tests showed that only 30% of HCDD cases are related to PCDs. We report the first known use of immunoglobulin heavy chain (IGH) gene rearrangement to diagnose a patient with γ3-HCDD, although bone marrow morphology test identified no abnormalities. Our findings provide strong evidence for a correlation between PCDs and HCDD, which could help understand the genetic background underlying abnormal heavy chains and assess disease prognosis. Further, concordant with previous findings, bortezomib-based chemotherapy had a good therapeutic effect in our patient. We summarize the experience of diagnosing and treating a case of HCDD, and combine this with a literature review to further explore the correlation between PCDs and HCDD, which has important clinical value.

Keywords: Immunoglobulin heavy chain gene rearrangement test; bortezomib; case report; genetic background; heavy chain deposition disease (HCDD); plasma cell disease.

Publication types

  • Case Reports
  • Review

MeSH terms

  • Antineoplastic Agents / therapeutic use
  • Bortezomib / therapeutic use
  • Genes, Immunoglobulin Heavy Chain*
  • Heavy Chain Disease* / diagnosis
  • Heavy Chain Disease* / drug therapy
  • Heavy Chain Disease* / genetics
  • Humans
  • Leukemia, Plasma Cell* / diagnosis
  • Leukemia, Plasma Cell* / genetics

Substances

  • Antineoplastic Agents
  • Bortezomib