You are in: eMedicine Specialties > Dermatology > ALLERGY AND IMMUNOLOGY Urticaria, DermographismArticle Last Updated: Feb 27, 2007AUTHOR AND EDITOR INFORMATIONAuthor: Simone Laube, MD, MRCP, Consulting Staff, Skin Centre, City Hospital, Birmingham, United Kingdom Editors: Shyam Verma, MBBS, DVD, FAAD, Adjunct Clinical Assistant Professor, Department of Dermatology, University of Virginia, SUNY at Stonybrook, Penn State Univ; Richard P Vinson, MD, Assistant Clinical Professor, Department of Dermatology, Texas Tech University School of Medicine; Consulting Staff, Mountain View Dermatology, PA; Paul Krusinski, MD, Director of Dermatology, Professor, Department of Internal Medicine, Fletcher Allen Health Care, University of Vermont; Catherine Quirk, MD, Clinical Assistant Professor, Department of Dermatology, Brown University; William D James, MD, Paul R Gross Professor of Dermatology, University of Pennsylvania School of Medicine; Vice-Chair, Program Director, Department of Dermatology, University of Pennsylvania Health System Author and Editor Disclosure Synonyms and related keywords: dermatographism, urticaria, urticarial dermographism, factitious urticaria, allergy, allergic reaction, anaphylaxis, anaphylactoid reaction, angioedema, triple response of Lewis, linear wheal, whealing, red dermatographism, red urticaria, skin scratch reactions, hives, itching INTRODUCTIONBackgroundDermographism is a normal physiological response of the skin. The term literally means writing on the skin. Firm stroking of the skin produces an initial red line (capillary dilatation), followed by an axon-reflex flare with broadening erythema (arteriolar dilatation) and the formation of a linear wheal (transudation of fluid/edema) termed the triple response of Lewis. An exaggerated response accompanied by itching to this constitutional whealing tendency is seen in approximately 2-5% of the population and is termed symptomatic dermographism. Dermographism is the most common form of physical urticaria.
PathophysiologyThe exact mechanism of dermographism remains uncertain. Trauma may release an antigen that interacts with the membrane-bound immunoglobulin E of mast cells, which release inflammatory mediators, particularly histamine, into the tissues. This causes small blood vessels to leak, allowing fluid to accumulate in the skin. Other mediators possibly involved are leukotrienes, heparin, bradykinin, kallikrein, and peptides such as substance P. FrequencyInternationalSymptomatic dermographism is the most common of the physical urticarias, affects approximately 2-5% of the population, and can occur with other forms of urticaria. Increased incidence has been reported in pregnancy (especially in second half), at the onset of menopause, in atopic children, and in patients with Behçet disease.1 Mortality/MorbiditySimple dermographism is the most common variant, and patients with this form are asymptomatic. However, other forms are associated with pruritus. Most people with dermographism are otherwise healthy. An association with thyroid disease has been described in some patients but remains controversial. RaceNo racial variance in prevalence is known. SexWhether a sexual variance in prevalence occurs is unclear. None has been consistently reported, although one study on dermographism in children reported a female predominance.2 AgeDermographism can appear in persons of any age but is more common in young adults. Peak incidence is in the second and third decades. CLINICALHistoryWhealing usually develops within 5 minutes of stroking the skin and persists for 15-30 minutes. A short refractory period after clearance of the wheal has been reported. Giant wheals can develop if deep extension of the swelling occurs.
PhysicalItching and whealing can affect all body surfaces, but the scalp and genitalia are less frequently involved. However, dyspareunia and vulvodynia have been reported in patients with symptomatic dermographism.3 Rarer forms of dermographism include the following:
CausesSymptomatic dermographism is usually idiopathic. It may have an immunologic basis in some patients. Passive transfer of the dermographic response with immunoglobulin E– or immunoglobulin M–containing serum has been reported but no allergen has been identified.
DIFFERENTIALSMastocytosis Urticaria, Chronic
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| Drug Name | Cetirizine (Zyrtec, Zyrtec Chewable Tablets) |
|---|---|
| Description | Forms complex with histamine for H1-receptor sites in blood vessels, GI tract, and respiratory tract. |
| Adult Dose | 10 mg PO qd |
| Pediatric Dose | <2 years: Not recommended 2-6 years: 5 mg PO qd or 2.5 mg PO bid >6 years: Administer as in adults |
| Contraindications | Documented hypersensitivity |
| Interactions | Increases toxicity of CNS depressants |
| Pregnancy | B - Fetal risk not confirmed in studies in humans but has been shown in some studies in animals |
| Precautions | Sedation and antimuscarinic effects (low); caution in hepatic or renal dysfunction; doses >10 mg/d may cause drowsiness |
| Drug Name | Loratadine (Claritin) |
|---|---|
| Description | Selectively inhibits peripheral histamine H1 receptors. |
| Adult Dose | 10 mg PO qd |
| Pediatric Dose | <2 years: Not recommended 2-12 years and <30 kg: 5 mg PO qd >30 kg: Administer as in adults |
| Contraindications | Documented hypersensitivity |
| Interactions | Ketoconazole, erythromycin, procarbazine, and alcohol may increase levels |
| Pregnancy | B - Fetal risk not confirmed in studies in humans but has been shown in some studies in animals |
| Precautions | Initiate therapy at lower dose in liver impairment |
| Drug Name | Desloratadine (Clarinex) |
|---|---|
| Description | Long-acting tricyclic histamine antagonist selective for H1 receptor. Relieves nasal congestion and systemic effects of seasonal allergy. Major metabolite of loratadine, which, after ingestion, is metabolized extensively to active metabolite 3-hydroxydesloratadine. |
| Adult Dose | 5 mg PO qd |
| Pediatric Dose | <12 years: Not established >12 years: Administer as in adults |
| Contraindications | Documented hypersensitivity |
| Interactions | Data are limited; erythromycin and ketoconazole increase desloratadine and 3-hydroxydesloratadine plasma concentrations, but no increase in clinically relevant adverse effects, including QTc, observed |
| Pregnancy | C - Fetal risk revealed in studies in animals but not established or not studied in humans; may use if benefits outweigh risk to fetus |
| Precautions | Decrease dose in hepatic impairment; rarely causes pharyngitis or dry mouth |
| Drug Name | Acrivastine (Semprex) |
|---|---|
| Description | Competes with histamine for H1 receptors on GI tract, blood vessels, and respiratory tract, reducing hypersensitivity reactions. |
| Adult Dose | 8 mg PO tid |
| Pediatric Dose | Not established |
| Contraindications | Documented hypersensitivity; within 14 d of initiating MAOI therapy; severe coronary disease; severe hypertension; elderly |
| Interactions | Guanethidine, methyldopa, reserpine, or beta-blockers may decrease effects; CNS depressants, alcohol, and sympathomimetics increase toxicity |
| Pregnancy | C - Fetal risk revealed in studies in animals but not established or not studied in humans; may use if benefits outweigh risk to fetus |
| Precautions | Sedation and antimuscarinic effects may occur; caution in high blood pressure, diabetes, ischemic heart disease, GI or GU obstruction, thyroid disease, prostatic hypertrophy, and increased intraocular pressure |
| Drug Name | Fexofenadine (Allegra) |
|---|---|
| Description | Competes with histamine for H1 receptors on GI tract, blood vessels, and respiratory tract, reducing hypersensitivity reactions. Does not sedate. |
| Adult Dose | 60 mg PO bid |
| Pediatric Dose | <12 years: Not recommended >12 years: Administer as in adults |
| Contraindications | Documented hypersensitivity |
| Interactions | Toxicity increases with coadministration of erythromycin and ketoconazole |
| Pregnancy | C - Fetal risk revealed in studies in animals but not established or not studied in humans; may use if benefits outweigh risk to fetus |
| Precautions | No data available on use while breastfeeding; may cause dizziness |
| Drug Name | Hydroxyzine (Atarax, Vistaril, Vistazine) |
|---|---|
| Description | Sedative antihistamine that is also anxiolytic. Antagonizes H1 receptors in periphery. May suppress histamine activity in subcortical region of CNS. |
| Adult Dose | Pruritus: 25 mg PO hs initially; increase prn to 25 mg PO tid/qid Anxiety: 50-100 mg PO qid |
| Pediatric Dose | <6 months: Not recommended 6 months to 6 years: 5-15 mg/d PO; increase to 50 mg/d PO divided tid/qid >6 years: 15-25 mg/d PO; increase to 50-100 mg/d PO divided tid/qid |
| Contraindications | Documented hypersensitivity |
| Interactions | May enhance response to alcohol, barbiturates, and other CNS depressants |
| Pregnancy | C - Fetal risk revealed in studies in animals but not established or not studied in humans; may use if benefits outweigh risk to fetus |
| Precautions | Associated with clinical exacerbations of porphyria (may not be safe for porphyria patients); ECG abnormalities (alterations in T waves) may occur; may cause drowsiness |
The authors and editors of eMedicine gratefully acknowledge the contributions of previous author, Elsbeth Young, MD, FRCP, to the development and writing of this article.
Urticaria, Dermographism excerpt
Article Last Updated: Feb 27, 2007