Relapsing angioedema

Authors

  • M. Branco Ferreira Assistente de Imunoalergologia, Serviço de Medicina III do Hospital de Santa Maria, Lisboa
  • Maria Helena Clode Chefe de Serviço de Imunoalergologia, Serviço de Medicina III do Hospital de Santa Maria, Lisboa
  • A. G. Palma Carlos Director de Serviço de Imunoalergologia Unidade de Jmunoalergologia, Serviço de Medicina III do Hospital de Santa Maria, Lisboa

Keywords:

angioedema, C1 inhibitor deficit, monoclonal gammopathy

Abstract

The authors present the case report of a male patient, with a rare and potentially lethal disease, angioedema, due to an acquired deficit of C1 esterase inhibitor, which lead to several emergency room admissions in the two years prior to admission. Additionally, this patient had two extremely rare findings in this type of disease: a normal C1q levai and a monoclonal gammopathy of unknown significance. The authors present a review of the literature of acquired angioedema and the associations with other diseases that are generally found in these patients.

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References

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Additional Files

Published

1999-06-30

How to Cite

1.
Branco Ferreira M, Clode MH, Palma Carlos AG. Relapsing angioedema. RPMI [Internet]. 1999 Jun. 30 [cited 2024 Dec. 18];6(2):103-6. Available from: https://revista.spmi.pt/index.php/rpmi/article/view/2051

Issue

Section

Case Reports

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