Diagnostics and exclusion of hereditary angioedema. A standarized approach for the practice;Diagnostik und ausschluss des hereditären angioödems: Ein standardisierter ansatz für die praxis

Hautarzt

Volumn 63, Issue 7, 2012, Pages 567-572

  Magerl, M ^a   Brasch, J ^b   Forster U ^a   Hauswald, B ^c   Mohr, B ^b   Praßler J ^d   Treudler, R ^e   Vetter, R ^f   Wahn, V ^a   Zampelli, V ^g   Ziemer, M ^f   Maurer, M ^a  

^a CHARITÉ UNIVERSITÄTSMEDIZIN BERLIN   (Germany)

^b UNIVERSITY HOSPITAL SCHLESWIG HOLSTEIN   (Germany)

^c UNIVERSITY HOSPITAL CARL GUSTAV CARUS   (Germany)

^d FRIEDRICH SCHILLER UNIVERSITY JENA   (Germany)

^e UNIVERSITY HOSPITAL LEIPZIG   (Germany)

^f Universitätsklinik für Dermatologie und Venerologie   (Germany)

^g DESSAU MEDICAL CENTER   (Germany)

Author keywords

Anamnestic algorithm; Angioedema; Bradykinin; C1 inhibitor; Diagnostic algorithm

Indexed keywords

BRADYKININ;

ALGORITHM; ANGIONEUROTIC EDEMA; ARTICLE; DIFFERENTIAL DIAGNOSIS; MAST CELL; MEDICAL PRACTICE;

EID: 84864350044     PISSN: 00178470     EISSN: 14321173     Source Type: Journal    
DOI: 10.1007/s00105-012-2388-x     Document Type: Article

References (38)

1. Bygum A (2009) Hereditary angio-oedema in Denmark: a nationwide survey. Br J Dermatol 161(5):1153-1158
2. Goring HD et al (1998) Hereditary angioedema in the German-speaking region. Hautarzt 49(2):114-122
3. Roche O et al (2005) Hereditary angioedema due to C1 inhibitor deficiency: patient registry and approach to the prevalence in Spain. Ann Allergy Asthma Immunol 94(4):498-503 (Pubitemid 40547939)
4. Romero DS, Di Marco P, Malbran A (2009) Hereditary angioedema. Family history and clinical manifestations in 58 patients. Medicina (B Aires) 69(6):601-606
5. Maurer M, Magerl M (2010) Hereditary angioedema: an update on available therapeutic options. J Dtsch Dermatol Ges 8(9):663-672
6. Bowen T et al (2010) International consensus algorithm for the diagnosis, therapy and management of hereditary angioedema. Allergy Asthma Clin Immunol 6(1):24
7. Gompels MM et al (2005) C1 inhibitor deficiency: consensus document. Clin Exp Immunol 139(3):379-394 (Pubitemid 40333248)
8. Bas M et al (2007) Nonallergic angioedema: role of bradykinin. Allergy 62(8):842-856 (Pubitemid 47037860)
9. Davis AE III (2005) The pathophysiology of hereditary angioedema. Clin Immunol 114(1):3-9 (Pubitemid 39646476)
10. Davis AE III, Mejia P, Lu F (2008) Biological activities of C1 inhibitor. Mol Immunol 45(16):4057-4063
11. Nussberger J et al (1998) Plasma bradykinin in angio-oedema. Lancet 351(9117):1693-1697 (Pubitemid 28254530)
12. Skidgel R, Erdos E (2006) Histamine, bradykinin, and their antagonists. In: H. JG, L. LE (Hrsg) Goodman and Gilman's the pharmacologic basis of therapeutics, Vol. 11. McGraw-Hill, New York
13. Agostoni A et al (2004) Hereditary and acquired angioedema: problems and progress: proceedings of the third C1 esterase inhibitor deficiency workshop and beyond. J Allergy Clin Immunol 114(3, Suppl 1):S51-S131 (Pubitemid 39200689)
14. Binkley KE (2010) Factor XII mutations, estrogen-dependent inherited angioedema, and related conditions. Allergy Asthma Clin Immunol 6(1):16
15. Bork K et al (2000) Hereditary angioedema with normal C1-inhibitor activity in women. Lancet 356(9225):213-217 (Pubitemid 30446977)
16. Breitbart SI, Bielory L (2010) Acquired angioedema: autoantibody associations and C1q utility as a diagnostic tool. Allergy Asthma Proc 31(5):428-434
17. Wagenaar-Bos IG et al (2008) Functional C1-inhibitor diagnostics in hereditary angioedema: assay evaluation and recommendations. J Immunol Methods 338(1-2):14-20
18. Bork K et al (2006) Hereditary angioedema: new findings concerning symptoms, affected organs, and course. Am J Med 119(3):267-274 (Pubitemid 43255068)
19. Bork K et al (2006) Symptoms, course, and complications of abdominal attacks in hereditary angioedema due to C1 inhibitor deficiency. Am J Gastroenterol 101(3):619-627 (Pubitemid 43340941)
20. Dirks K, Deuerling J, Lutz H (2001) Sonography in hereditary angioedema: typical findings demonstrated by the example of 3 cases. Ultraschall Med 22(4):186-190 (Pubitemid 32843775)
21. Wakisaka M et al (2008) Computed tomography of the gastrointestinal manifestation of hereditary angioedema. Radiat Med 26(10):618-621
22. Prematta MJ et al (2009) Frequency, timing, and type of prodromal symptoms associated with hereditary angioedema attacks. Allergy Asthma Proc 30(5):506-511
23. Bork K (2010) Diagnosis and treatment of hereditary angioedema with normal C1 inhibitor. Allergy Asthma Clin Immunol 6(1):15
24. Bouillet L (2010) Hereditary angioedema in women. Allergy Asthma Clin Immunol 6(1):17
25. Krassilnikova S, Craig ET, Craig TJ (2010) Summary of the International Multicenter Prospective Angioedema C1-inhibitor Trials 1 and 2(IMPACT1 and 2). Expert Rev Clin Immunol 6 (3):327-334
26. Bork K et al (2007) Treatment of acute edema attacks in hereditary angioedema with a bradykinin receptor-2 antagonist (Icatibant). J Allergy Clin Immunol 119(6):1497-1503 (Pubitemid 46855846)
27. Cicardi M et al (2010) Icatibant, a new bradykinin-receptor antagonist, in hereditary angioedema. N Engl J Med 363(6):532-541
28. Krause K et al (2010) Successful treatment of hereditary angioedema with bradykinin B2-receptor antagonist icatibant. J Dtsch Dermatol Ges 8(4):272-274
29. Cicardi M et al (2010) Ecallantide for the treatment of acute attacks in hereditary angioedema. N Engl J Med 363(6):523-531
30. Choi G et al (2007) Recombinant human C1-inhibitor in the treatment of acute angioedema attacks. Transfusion 47(6):1028-1032 (Pubitemid 46802091)
31. Zuraw BL et al (2010) Nanofiltered C1 inhibitor concentrate for treatment of hereditary angioedema. N Engl J Med 363(6):513-522
32. Boyle RJ, Nikpour M, Tang ML (2005) Hereditary angio-oedema in children: a management guideline. Pediatr Allergy Immunol 16(4):288-294 (Pubitemid 40868483)
33. Farkas H (2010) Pediatric hereditary angioedema due to C1-inhibitor deficiency. Allergy Asthma Clin Immunol 6(1):18
34. Zingale LC et al (2006) Angioedema without urticaria: a large clinical survey. CMAJ 175(9):1065-1070 (Pubitemid 44683294)
35. Cicardi M, Zanichelli A (2010) Acquired angioedema. Allergy Asthma Clin Immunol 6(1):14
36. Karim Y, Griffiths H, Deacock S (2004) Normal complement C4 values do not exclude hereditary angioedema. J Clin Pathol 57(2):213-214 (Pubitemid 38177769)
37. Tarzi MD et al (2007) An evaluation of tests used for the diagnosis and monitoring of C1 inhibitor deficiency: normal serum C4 does not exclude hereditary angio-oedema. Clin Exp Immunol 149(3):513-516 (Pubitemid 47256155)
38. Cichon S et al (2006) Increased activity of coagulation factor XII (Hageman factor) causes hereditary angioedema type III. Am J Hum Genet 79(6):1098-1104 (Pubitemid 44853481)