[Acquired C1 esterase inhibitor deficiency via bradykinin-mediated angioedema: Four cases]

Ann Dermatol Venereol. 2018 Oct;145(10):598-602. doi: 10.1016/j.annder.2018.02.012. Epub 2018 Apr 17.
[Article in French]

Abstract

Background: Acquired C1-esterase inhibitor (C1-INH) deficiency angioedema (C1-INH-AAE) is a form of bradykinin-mediated angioedema. This rare disorder is due to acquired consumption of C1-INH, hyperactivation of the classic pathway of human complement, and potentially fatal recurrent angioedema symptoms. Clinical symptoms of C1-INH-AAE are very similar to those of hereditary angioedema (HAE) but usually appear after the fourth decade of life and induce abdominal pain less frequently. Laboratory tests are essential in establishing the diagnosis with low levels or abnormal structure and function of C1-INH. Most patients present C1-INH autoantibodies. Furthermore, C1q is reduced in AAE, contrary to HAE. The long-term prognosis is determined by associated hematologic malignancies.

Patients and methods: We report 4 cases of C1-INH-AAE associated with lymphoproliferative disorders referred to the Reference Centre for Angioedema of Besançon, France. The patients were aged between 60 and 77 years. C1 INH antibodies were found in three patients. Symptoms were triggered by angiotensin-converting enzyme (ACE) inhibitors or angiotensin II receptor blockers (ARBs) in 3 patients. Hematologic malignancy was present at diagnosis (one case of chronic lymphoid leukemia) or was diagnosed during follow-up (one case of indolent marginal zone non-Hodgkin lymphoma and two cases of monoclonal gammopathy).

Discussion: C1-INH-AAE induced by ACE inhibitors or ARBs may be associated with hematologic malignancies. This form of revelation does not necessarily indicate a diagnosis of ACE or ARBs angioedema, and screening should therefore be performed for C1 Inh and C1q. An underlying hematologic malignancy should be routinely sought and the long-term prognosis determined.

Keywords: Acquired bradykinin-mediated angioedema; Angiœdème bradykinique acquis; Anticorps anti-C1 inhibiteur; C1-inhibitor antibodies; C1-inhibitor deficiency; Déficit en C1 inhibiteur; Hémopathie maligne; Malignant hemopathy.

Publication types

  • Case Reports

MeSH terms

  • Abdominal Pain / etiology
  • Aged
  • Angioedema / chemically induced
  • Angioedema / diagnosis
  • Angioedema / etiology*
  • Angioedema / immunology
  • Angioedemas, Hereditary / diagnosis
  • Angiotensin II Type 1 Receptor Blockers / adverse effects
  • Angiotensin-Converting Enzyme Inhibitors / adverse effects
  • Autoantibodies / immunology*
  • Autoimmune Diseases / chemically induced
  • Autoimmune Diseases / diagnosis
  • Autoimmune Diseases / etiology*
  • Autoimmune Diseases / immunology
  • Bradykinin / physiology*
  • Complement C1 Inhibitor Protein / immunology*
  • Female
  • Humans
  • Leukemia, Lymphocytic, Chronic, B-Cell / complications*
  • Leukemia, Lymphocytic, Chronic, B-Cell / immunology
  • Lymphoma, B-Cell, Marginal Zone / complications*
  • Lymphoma, B-Cell, Marginal Zone / immunology
  • Male
  • Middle Aged
  • Paraproteinemias / complications*
  • Paraproteinemias / immunology

Substances

  • Angiotensin II Type 1 Receptor Blockers
  • Angiotensin-Converting Enzyme Inhibitors
  • Autoantibodies
  • Complement C1 Inhibitor Protein
  • Bradykinin