Light chain deposition disease with predominant hepatic involvement – a clinical case report

Authors

  • Susana Costa Serviço de Medicina II dos Hospitais da Universidade de Coimbra
  • Patrícia Dias Serviço de Medicina II dos Hospitais da Universidade de Coimbra
  • Elsa Gaspar Serviço de Medicina II dos Hospitais da Universidade de Coimbra
  • Maria Augusta Cipriano Serviço de Medicina II dos Hospitais da Universidade de Coimbra
  • Francisco Parente Serviço de Medicina II dos Hospitais da Universidade de Coimbra
  • Alberto Lourenço Serviço de Medicina II dos Hospitais da Universidade de Coimbra
  • Borges Alexandrino Serviço de Medicina II dos Hospitais da Universidade de Coimbra
  • J. J. Alves de Moura Director de Serviço, Serviço de Medicina II dos Hospitais da Universidade de Coimbra; Professor da Faculdade de Medicina

Keywords:

Lightchain deposition disease

Abstract

Light chain deposition disease (LCDD) is one of the least common
of the monoclonal plasma cell dyscrasias. It is characterized by
multi-systemic infi ltrative light chains, with the kidney being
almost always involved. Isolated liver involvement is rare and this
organ is usually affected in patients who also have renal disease,
dysfunction of which is the commonest clinical presentation. The
authors report a patient who presented LCDD with predominantly
hepatic involvement.

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References

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Additional Files

Published

2006-09-29

How to Cite

1.
Costa S, Dias P, Gaspar E, Cipriano MA, Parente F, Lourenço A, Alexandrino B, Alves de Moura JJ. Light chain deposition disease with predominant hepatic involvement – a clinical case report. RPMI [Internet]. 2006 Sep. 29 [cited 2024 May 17];13(3):172-8. Available from: https://revista.spmi.pt/index.php/rpmi/article/view/1642

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Case Reports

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