Vasculitis complicating Cystic Fibrosis (CF) has been rarely reported. We describe a case of CF patient with a generalised Schoenlein-Henoch Purpura (SHP) characterised by neurological, kydney and cardiac involvement. Given the immunological origin of the vasculitis, CF patients present some conditions that can induce an hyperergic immune response: bronchial chronic microbial infection, prolonged antibiotic treatment, pancreatic enzymes, bronchodilators, mucolytics and other drugs, are factors that represent a considerable antigenic reserve, on the other hand, the constant increase of serum immunoglobulin levels and sometimes of circulating immunecomplexes seem to facilitate the onset of vasculitis, especially SHP, in this group of patients.
Sindrome di Schoenlein-Henoch / L. Gnecchi, P. Randi, G. Rizzitelli, S. Veraldi - In: Dermatologia clinica : 300 casi inusuali presentati agli “Incontri Dermatologici” di Segrate / T. Cainelli, L. Marchesi. - Milano : McGraw-Hill Libri Italia, 2000. - ISBN 8838629595. - pp. 298-299
Sindrome di Schoenlein-Henoch
S. VeraldiUltimo
2000
Abstract
Vasculitis complicating Cystic Fibrosis (CF) has been rarely reported. We describe a case of CF patient with a generalised Schoenlein-Henoch Purpura (SHP) characterised by neurological, kydney and cardiac involvement. Given the immunological origin of the vasculitis, CF patients present some conditions that can induce an hyperergic immune response: bronchial chronic microbial infection, prolonged antibiotic treatment, pancreatic enzymes, bronchodilators, mucolytics and other drugs, are factors that represent a considerable antigenic reserve, on the other hand, the constant increase of serum immunoglobulin levels and sometimes of circulating immunecomplexes seem to facilitate the onset of vasculitis, especially SHP, in this group of patients.Pubblicazioni consigliate
I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.