eMedicine Specialties > Allergy and Immunology > Urticaria and Angioedema
Angioedema: Differential Diagnoses & Workup
Updated: Oct 20, 2008
- Overview
- Differential Diagnoses & Workup
- Treatment & Medication
- Follow-up
- Multimedia
Differential Diagnoses
Other Problems to Be Considered
Allergic
Inhalants
Bites and stings
Natural rubber latex
Foods (eg, milk, eggs, peanuts, tree nuts, soy, wheat, seafood, sulfites)
Drugs
ACE inhibitors
Beta-lactam antibiotics
Sulfonamides
Aspirin/nonsteroidal anti-inflammatory drugs
Insulin
Dilantin
Streptokinase
Viral infections
Herpes simplex
Hepatitis B
Hepatitis C
Mononucleosis
Coxsackieviruses A and B
Bacterial infections
Dental caries/abscesses
Pharyngitis
Tonsillitis
Sinusitis
Otitis media
Upper respiratory infection
Urinary tract infection
Parasitic infections
Ascaris species
Strongyloides species
Echinococcus species
Toxocara species
Fasciola species
Filaria species
Schistosoma species
Workup
Laboratory Studies
- Laboratory evaluation of the complement system is essential to diagnose HAE or AAE.
- In type I HAE, C1-INH and C4 levels are low. C4 levels are low during an attack; they may be normal in between attacks.
- In type II HAE, which is characterized by normal levels of C1-INH that is dysfunctional, a functional or qualitative assay of C1-INH must be performed before the diagnosis can be excluded. C4 levels are low during an attack.
- In type III HAE, C1-INH levels and function and C4 levels are normal at all times.
- In HAE and AAE, C4 levels are low during angioedema episodes but may be normal in between episodes. C4 can be used for screening between angioedema episodes, with the understanding that a normal level does not rule out the diagnosis.
- To differentiate between AAE and HAE, the C1q level should be measured. The hallmarks of AAE are low C1q, C2, C4, and C1-INH levels. In HAE, C1q levels are usually normal or only slightly decreased. Levels of C1q are rarely less than 50% of the normal values in HAE; in AAE, C1q levels are less than 10% of the normal values.
- Complete blood cell count: Leukocytosis should be absent. If leukocytosis is present, an infectious etiology should be sought. The white blood cell count may be elevated secondary to hemoconcentration.
- Electrolytes: Abnormalities may be present secondary to vomiting and diarrhea. Prerenal renal failure can also result from intravascular volume depletion.
- If time permits, a blood sample should be submitted for a type and crossmatch and for determination of the prothrombin time and activated partial thromboplastin time before surgical airway intervention is instituted.
Imaging Studies
- Plain abdominal films may show a "stacked coin" or "thumbprint" appearance of the intestines.
- A chest film may show pleural effusion.
- A soft tissue neck film may show soft tissue swelling.
- A CT scan image of the abdomen may show severe edema of the bowel wall.
Procedures
- Airway protection is the most important consideration in patients with angioedema. In cases of possible airway compromise, early intervention with intubation may be preferred. Intubation may be exceedingly difficult, and advanced techniques (eg, fiberoptic intubation) may be necessary. In severe cases of laryngeal edema, a surgical airway must be created via cricothyrotomy or tracheotomy.
More on Angioedema |
| Overview: Angioedema |
Differential Diagnoses & Workup: Angioedema |
| Treatment & Medication: Angioedema |
| Follow-up: Angioedema |
| Multimedia: Angioedema |
| References |
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References
Agah R, Bandi V, Guntupalli KK. Angioedema: the role of ACE inhibitors and factors associated with poor clinical outcome. Intensive Care Med. Jul 1997;23(7):793-6. [Medline].
Agostoni A, Cicardi M. Drug-induced angioedema without urticaria. Drug Saf. 2001;24(8):599-606. [Medline].
Agostoni A, Aygören-Pürsün E, Binkley KE, et al. Hereditary and acquired angioedema: problems and progress: proceedings of the third C1 esterase inhibitor deficiency workshop and beyond. J Allergy Clin Immunol. Sep 2004;114(3 Suppl):S51-131. [Medline].
Bork K, Barnstedt SE, Koch P, Traupe H. Hereditary angioedema with normal C1-inhibitor activity in women. Lancet. Jul 15 2000;356(9225):213-7. [Medline].
Bowen T, Cicardi M, Farkas H, et al. Canadian 2003 International Consensus Algorithm For the Diagnosis, Therapy, and Management of Hereditary Angioedema. J Allergy Clin Immunol. Sep 2004;114(3):629-37. [Medline].
Ebo DG, Stevens WJ. Hereditary angioneurotic edema: review of the literature. Acta Clin Belg. Jan-Feb 2000;55(1):22-9. [Medline].
Farkas H, Harmat G, Füst G, et al. Clinical management of hereditary angio-oedema in children. Pediatr Allergy Immunol. Jun 2002;13(3):153-61. [Medline].
Fay A, Abinun M. Current management of hereditary angio-oedema (C'1 esterase inhibitor deficiency). J Clin Pathol. Apr 2002;55(4):266-70. [Medline].
Frigas E. Angioedema with acquired deficiency of the C1 inhibitor: a constellation of syndromes. Mayo Clin Proc. Oct 1989;64(10):1269-75. [Medline].
Gaboriau HP, Solomon JW. Angioneurotic edema. J La State Med Soc. Feb 1997;149(2):50-2. [Medline].
Heymann WR. Acquired angioedema. J Am Acad Dermatol. Apr 1997;36(4):611-5. [Medline].
Howes LG, Tran D. Can angiotensin receptor antagonists be used safely in patients with previous ACE inhibitor-induced angioedema?. Drug Saf. 2002;25(2):73-6. [Medline].
Kyrmizakis DE, Papadakis CE, Liolios AD, et al. Angiotensin-converting enzyme inhibitors and angiotensin II receptor antagonists. Arch Otolaryngol Head Neck Surg. Dec 2004;130(12):1416-9.
Markovic SN, Inwards DJ, Frigas EA, Phyliky RP. Acquired C1 esterase inhibitor deficiency. Ann Intern Med. Jan 18 2000;132(2):144-50. [Medline].
Moore GP, Hurley WT, Pace SA. Hereditary angioedema. Ann Emerg Med. Oct 1988;17(10):1082-6. [Medline].
Nzeako UC, Frigas E, Tremaine WJ. Hereditary angioedema: a broad review for clinicians. Arch Intern Med. Nov 12 2001;161(20):2417-29. [Medline].
Rodgers GK, Galos RS, Johnson JT. Hereditary angioedema: case report and review of management. Otolaryngol Head Neck Surg. Mar 1991;104(3):394-8. [Medline].
Shah UK, Jacobs IN. Pediatric angioedema: ten years' experience. Arch Otolaryngol Head Neck Surg. Jul 1999;125(7):791-5. [Medline].
Sim TC, Grant JA. Hereditary angioedema: its diagnostic and management perspectives. Am J Med. Jun 1990;88(6):656-64. [Medline].
Waytes AT, Rosen FS, Frank MM. Treatment of hereditary angioedema with a vapor-heated C1 inhibitor concentrate. N Engl J Med. Jun 20 1996;334(25):1630-4. [Medline].
Zirkle M, Bhattacharyya N. Predictors of airway intervention in angioedema of the head and neck. Otolaryngol Head Neck Surg. Sep 2000;123(3):240-5. [Medline].
Further Reading
Keywords
angioneurotic edema, oedema, laryngeal edema, hereditary angioedema, HAE, acquired angioedema, AAE, allergic reactions, hereditary angioneurotic edema, airway obstruction, swelling
Differential Diagnoses & Workup: Angioedema