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Malignancy and Immune Disorders in Patients With Hereditary Angioedema
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Abstract
Background
With the advent of new therapies, patients with hereditary angioedema (HAE) are living longer lives. Although complement dysregulation has been linked to various disease states, it is currently not known if HAE patients are at an increased risk of developing malignancy or autoimmune conditions.
Case Presentation
: We reviewed the charts of 49 HAE patients and identified 6 patients who had a co-existing malignancy diagnosis (two with breast cancer, one with melanoma, one with pancreatic cancer, one with renal cancer and one with cervical dysplasia) and 6 patients who had a diagnosis of a co-existing immune disorder (two with rheumatoid arthritis, two with ulcerative colitis, one with chronic urticaria with hypothyroidism and one with Sjogren’s syndrome). Nearly all malignancy cases occurred in older HAE patients (> 50 years) and malignancy was diagnosed before HAE in 3 of the patients.
Conclusions
Our case series has identified multiple hereditary angioedema (HAE) patients with co-existing malignancy and immune disorders. Based on these findings, we would advocate that physicians managing HAE patients should maintain a high index of suspicion for these conditions.
Title: Malignancy and Immune Disorders in Patients With Hereditary Angioedema
Description:
Abstract
Background
With the advent of new therapies, patients with hereditary angioedema (HAE) are living longer lives.
Although complement dysregulation has been linked to various disease states, it is currently not known if HAE patients are at an increased risk of developing malignancy or autoimmune conditions.
Case Presentation
: We reviewed the charts of 49 HAE patients and identified 6 patients who had a co-existing malignancy diagnosis (two with breast cancer, one with melanoma, one with pancreatic cancer, one with renal cancer and one with cervical dysplasia) and 6 patients who had a diagnosis of a co-existing immune disorder (two with rheumatoid arthritis, two with ulcerative colitis, one with chronic urticaria with hypothyroidism and one with Sjogren’s syndrome).
Nearly all malignancy cases occurred in older HAE patients (> 50 years) and malignancy was diagnosed before HAE in 3 of the patients.
Conclusions
Our case series has identified multiple hereditary angioedema (HAE) patients with co-existing malignancy and immune disorders.
Based on these findings, we would advocate that physicians managing HAE patients should maintain a high index of suspicion for these conditions.
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