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Urticaria, Chronic: Differential Diagnoses & Workup

Author: Daniel J Hogan, MD, Clinical Professor of Internal Medicine (Dermatology), NOVA Southeastern University; Investigator, Hill Top Research, Florida Research Center
Contributor Information and Disclosures

Updated: Oct 23, 2009

Differential Diagnoses

Acute Febrile Neutrophilic Dermatosis
Mastocytosis
Atopic Dermatitis
Muckle-Wells syndrome
Bedbug Bites
Pruritic Urticarial Papules and Plaques of Pregnancy
Bullous Pemphigoid
Reticular erythematosus mucinosis
Chronic infantile neurologic cutaneous articular syndrome
Scabies
Contact Dermatitis, Allergic
Schnitzler Syndrome
Erythema Multiforme
Urticarial Vasculitis
Familial cold autoinflammatory syndrome
Wells Syndrome (Eosinophilic Cellulitis)
Fixed Drug Eruptions
Insect Bites
Lupus Erythematosus, Subacute Cutaneous

Other Problems to Be Considered

Melkersson-Rosenthal syndrome

Workup

Laboratory Studies

Elicit a history and perform a physical examination and challenge testing for physical causes in patients with chronic urticaria. Direct the selection of laboratory tests using the information elicited from the history and physical examination.

  • Complete blood cell count with differential: Patients with parasitic infections, especially in developing countries, or patients experiencing a drug reaction may have an elevated eosinophil count. The absence of blood eosinophilia may obviate the necessity for stool examination for ova.
  • Erythrocyte sedimentation rate: It may be elevated in persons with urticarial vasculitis.
  • Hepatitis B and C titers: Both hepatitis B and C may be associated with cryoglobulinemia, which is associated with some forms of cold-induced urticaria and urticarial vasculitis. In addition, an association has been reported between hepatitis C and chronic urticaria.14
  • Antinuclear antibody titers: These are indicated in patients in whom urticarial vasculitis is suggested.
  • Erythrocyte sedimentation rate, C-reactive protein, antinuclear antibody, and rheumatoid factor: Testing should be performed if an underlying rheumatologic disorder is suspected.
  • Stool ova and parasites: Consider this test in patients with GI tract symptoms, an elevated eosinophil count, or a positive travel history.
  • Serum cryoglobulins: Cryoglobulinemia is associated with some forms of cold-induced urticaria.
  • Complement studies: C3 (associated with pulmonary involvement in a subset of patients with urticarial vasculitis), C4 (may be low in hereditary angioedema), and C1-esterase inhibitor (hereditary angioedema) functional assays may be performed.
  • Thyroid function, antithyroid microsomal, and peroxidase antibody titers: Patients with urticaria unresponsive to antihistamines or steroids may have elevated titers, which may respond to thyroid hormone therapy.15 Patients may be euthyroid. Urticaria is also more common in patients with Hashimoto thyroiditis. If antithyroglobulin and antimicrosomal antibodies are present, this supports the diagnosis of chronic immunologic urticaria. The plasma level of thyrotropin helps screen for thyroid dysfunction.
  • CU Index (Chronic Urticaria Index) is available from a few reference laboratories. Patients with a chronic form of urticaria with a positive functional anti-FcεR test result likely have an autoimmune basis for their disease. A positive result does not indicate which autoantibody (anti-IgE, anti-FcεRI, or anti-FcεRII) is present. This test is usually combined with thyroid function, antithyroid microsomal titers, and peroxidase antibody titers.

Other Tests

  • Challenge testing: Challenge testing may be required to exclude a physical urticaria.
  • Skin biopsy: Histologic examination is not necessary for the diagnosis urticaria. A biopsy is necessary for the diagnosis of urticarial vasculitis or a neutrophil-predominant pattern of urticaria that may not respond well to antihistamines. A skin biopsy is indicated when individual urticarial lesions persist for more than 24 hours or have associated petechiae or purpura and in patients with systemic symptoms such as fever, arthralgia, or arthritis. Histological evidence of leukocytoclasia (neutrophilic infiltration with fragmentation of nuclei) is a characteristic feature of urticarial vasculitis. The presence of neutrophils may indicate potential benefit from treatment with dapsone or colchicine.
  • Prick or radioallergosorbent assay testing: This might be useful if contact urticaria is suggested.
  • Skin prick testing: Results may help identify a food allergy, which is a rare cause of chronic urticaria.

Histologic Findings

Dermal edema, blood vessel dilatation, and mild perivascular infiltrate predominantly consisting of monocytes and CD4+ lymphocytes are characteristic findings; some forms exist in which neutrophils predominate.

More on Urticaria, Chronic

Overview: Urticaria, Chronic
Differential Diagnoses & Workup: Urticaria, Chronic
Treatment & Medication: Urticaria, Chronic
Follow-up: Urticaria, Chronic
References

References

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Further Reading

Keywords

chronic urticaria, hives, wheals, allergy, allergic reaction, anaphylaxis, anaphylactoid reaction, angioedema

Contributor Information and Disclosures

Author

Daniel J Hogan, MD, Clinical Professor of Internal Medicine (Dermatology), NOVA Southeastern University; Investigator, Hill Top Research, Florida Research Center
Daniel J Hogan, MD is a member of the following medical societies: Alpha Omega Alpha, American Academy of Dermatology, American Contact Dermatitis Society, and Canadian Dermatology Association
Disclosure: Nothing to disclose.

Medical Editor

Robert A Schwartz, MD, MPH, Professor and Head, Dermatology, Professor of Pathology, Pediatrics, Medicine, and Preventive Medicine and Community Health, UMDNJ-New Jersey Medical School
Robert A Schwartz, MD, MPH is a member of the following medical societies: Alpha Omega Alpha, American Academy of Dermatology, American College of Physicians, and Sigma Xi
Disclosure: Nothing to disclose.

Pharmacy Editor

Richard P Vinson, MD, Assistant Clinical Professor, Department of Dermatology, Texas Tech University School of Medicine; Consulting Staff, Mountain View Dermatology, PA
Richard P Vinson, MD is a member of the following medical societies: American Academy of Dermatology, Association of Military Dermatologists, Texas Dermatological Society, and Texas Medical Association
Disclosure: Nothing to disclose.

Managing Editor

Warren R Heymann, MD, Head, Division of Dermatology, Professor, Department of Internal Medicine, University of Medicine and Dentistry of New Jersey
Warren R Heymann, MD is a member of the following medical societies: American Academy of Dermatology, American Society of Dermatopathology, and Society for Investigative Dermatology
Disclosure: Nothing to disclose.

CME Editor

Catherine M Quirk, MD, Clinical Assistant Professor, Department of Dermatology, University of Pennsylvania
Catherine M Quirk, MD is a member of the following medical societies: Alpha Omega Alpha and American Academy of Dermatology
Disclosure: Nothing to disclose.

Chief Editor

Dirk M Elston, MD, Director, Department of Dermatology, Geisinger Medical Center
Dirk M Elston, MD is a member of the following medical societies: American Academy of Dermatology
Disclosure: Nothing to disclose.

 
 
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