Literature DB >> 17060655

Angioedema without urticaria: a large clinical survey.

Lorenza C Zingale1, Laura Beltrami, Andrea Zanichelli, Lorena Maggioni, Emanuela Pappalardo, Benedetta Cicardi, Marco Cicardi.   

Abstract

BACKGROUND: Angioedema without major urticarial flares (hives) is poorly understood. Its causes are diverse, and little is known about its pathogenic mechanisms. We report on our 11 years of experience with this condition and propose a classification of patients affected by angioedema unaccompanied by urticaria.
METHODS: From 1993 through 2003 at our outpatient clinic, 929 consecutive patients were examined for recurrent angioedema unaccompanied by urticaria. A detailed history was taken to identify known causes of angioedema, with special attention to external allergenic agents. Each patient underwent a complete physical examination, routine laboratory tests (blood cell count, protein electrophoresis, erythrosedimentation rate, examination of stool for ova and parasites, pharyngeal and urine cultures, sinus and dental radiography, and measurements of antitissue autoantibodies and rheumatoid factor in plasma), and complement parameters (C1 inhibitor, C4 and C1q). Further testing was done when pertinent, based on clinical findings. When all results were negative, response to H1-antihistamine was considered.
RESULTS: Angioedema could not be classified in 153 patients who were lost to follow-up (16.4%). Among the 776 cases with adequate data, these types of angioedema were identified: 124 (16%) related to external agents such as a drug, insect bite or foodstuff; 85 (11%) related to treatment with angiotensin-converting enzyme inhibitor; 55 (7%) associated with an autoimmune disease or infection; and 197 (25%) caused by C1 inhibitor deficiency. In the other 315 cases (41%), the etiology was undiscovered: 254 cases (33% of the study sample) were idiopathic histaminergic; 40 (5%) were idiopathic nonhistaminergic; and 21 (3%) had other causes of peripheral or generalyzed edema.
INTERPRETATION: Our data indicated that angioedema without urticaria could be classified according to specific clinical and pathogenic characteristics, and we have suggested a work-up for patients experiencing this condition.

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Year:  2006        PMID: 17060655      PMCID: PMC1609157          DOI: 10.1503/cmaj.060535

Source DB:  PubMed          Journal:  CMAJ        ISSN: 0820-3946            Impact factor:   8.262


  39 in total

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Journal:  J Allergy Clin Immunol       Date:  2004-09       Impact factor: 10.793

2.  The systemic capillary leak syndrome: appearance of interleukin-2-receptor-positive cells during attacks.

Authors:  M Cicardi; M Gardinali; G Bisiani; A Rosti; P Allavena; A Agostoni
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Authors:  A Leznoff; G L Sussman
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Review 4.  Autoantibodies and lymphoproliferative diseases in acquired C1-inhibitor deficiencies.

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5.  Angioedema associated with angiotensin-converting enzyme inhibitor use: outcome after switching to a different treatment.

Authors:  Marco Cicardi; Lorenza C Zingale; Luigi Bergamaschini; Angelo Agostoni
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Review 6.  Chronic urticaria: pathogenesis and treatment.

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Authors:  Tom Bowen; Marco Cicardi; Henriette Farkas; Konrad Bork; Wolfhart Kreuz; Lorenza Zingale; Lilian Varga; Inmaculada Martinez-Saguer; Emel Aygören-Pürsün; Karen Binkley; Bruce Zuraw; Alvin Davis; Jacques Hebert; Bruce Ritchie; Jeanne Burnham; Anthony Castaldo; Alejandra Menendez; Istvan Nagy; George Harmat; Christoph Bucher; Gina Lacuesta; Andrew Issekutz; Richard Warrington; William Yang; John Dean; Amin Kanani; Donald Stark; Christine McCusker; Eric Wagner; Georges-Etienne Rivard; Eric Leith; Ellie Tsai; Michael MacSween; John Lyanga; Bazir Serushago; Art Leznoff; Susan Waserman; Jean de Serres
Journal:  J Allergy Clin Immunol       Date:  2004-09       Impact factor: 10.793

8.  Autoimmune C1 inhibitor deficiency: report of eight patients.

Authors:  M Cicardi; G Bisiani; M Cugno; P Späth; A Agostoni
Journal:  Am J Med       Date:  1993-08       Impact factor: 4.965

9.  Kinin formation in hereditary angioedema plasma: evidence against kinin derivation from C2 and in support of "spontaneous" formation of bradykinin.

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10.  Hypocomplementemic urticarial vasculitis syndrome. Clinical and serologic findings in 18 patients.

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  39 in total

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2.  Unilateral mass-like pharyngeal and laryngeal angioedema.

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Review 3.  Hereditary angioedema in childhood: an approach to management.

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4.  Use of 5-deazaFAD to study hydrogen transfer in the D-amino acid oxidase reaction.

Authors:  L B Hersh; M S Jorns
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Review 5.  Recurrent angioedema and the threat of asphyxiation.

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6.  Drug-induced angioedema: experience of Italian emergency departments.

Authors:  G Bertazzoni; M T Spina; M G Scarpellini; F Buccelletti; M De Simone; M Gregori; V Valeriano; F R Pugliese; M P Ruggieri; M Magnanti; B Susi; L Minetola; L Zulli; F D'Ambrogio
Journal:  Intern Emerg Med       Date:  2013-11-09       Impact factor: 3.397

7.  ACE-inhibitor induced angio-oedema treated with complement C1-inhibitor concentrate.

Authors:  Eva Rye Rasmussen; Anette Bygum
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8.  Hereditary angioedema: New therapeutic options for a potentially deadly disorder.

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9.  2010 International consensus algorithm for the diagnosis, therapy and management of hereditary angioedema.

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10.  Urticaria and infections.

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