[Acquired angioedema with C1-INH deficiency and accompanying chronic spontaneous urticaria in a patient with chronic lymphatic B cell leukemia]

Hautarzt. 2015 Oct;66(10):723-5. doi: 10.1007/s00105-015-3679-9.
[Article in German]

Abstract

Acquired angioedema due to C1 inhibitor deficiency (C1-INH-AAE) is characterized by recurrent edema of the subcutaneous and/or submucosal tissue without wheals and negative family history of angioedema. Here, we present the case of a patient with a chronic lymphatic B cell leukemia who suffered from both C1-INH-AAE and chronic spontaneous urticaria. Oral corticosteroids, antihistamines, and the anti-IgE antibody omalizumab were applied to treat the chronic urticaria in combination with the plasma-derived C1 esterase inhibitor concentrate Berinert® and the bradykinin B2 receptor antagonist icatibant, but the symptoms did not improved significantly. Thus, polychemotherapy targeting the slow-growing lymphoproliferative disease including rituximab was initiated, which resulted in remission of both the urticaria and the angioedema.

Keywords: Icatibant; Lymphoproliferative disorders; Omalizumab; Rituximab; Urticaria.

Publication types

  • Case Reports
  • English Abstract

MeSH terms

  • Angioedema / complications*
  • Angioedema / diagnosis
  • Angioedema / drug therapy
  • Antineoplastic Agents / administration & dosage
  • Chronic Disease
  • Complement C1 Inactivator Proteins / deficiency*
  • Diagnosis, Differential
  • Drug Therapy, Combination / methods
  • Humans
  • Immunosuppressive Agents / administration & dosage
  • Leukemia, Lymphocytic, Chronic, B-Cell / complications*
  • Leukemia, Lymphocytic, Chronic, B-Cell / diagnosis
  • Leukemia, Lymphocytic, Chronic, B-Cell / drug therapy*
  • Male
  • Middle Aged
  • Omalizumab / administration & dosage
  • Rituximab / administration & dosage
  • Treatment Outcome
  • Urticaria / diagnosis
  • Urticaria / drug therapy*
  • Urticaria / etiology*

Substances

  • Antineoplastic Agents
  • Complement C1 Inactivator Proteins
  • Immunosuppressive Agents
  • Omalizumab
  • Rituximab