You are in: eMedicine Specialties > Dermatology > PSYCHOCUTANEOUS DISEASES Dermatitis ArtefactaArticle Last Updated: Aug 24, 2007AUTHOR AND EDITOR INFORMATIONAuthor: John YM Koo, MD, Vice Chair, Department of Dermatology, University of California San Francisco Medical Center; Professor, Clinical Dermatology, Department of Dermatology, University of California at San Francisco School of Medicine John YM Koo is a member of the following medical societies: American Academy of Dermatology, American Psychiatric Association, and National Psoriasis Foundation Coauthor(s): Patricia T Ting, MD, Staff Physician, Department of Medicine, University of Calgary Editors: Jacek C Szepietowski, MD, PhD, Professor and Vice-Head, Department of Dermatology, Venereology and Allergology, Wroclaw Medical University, Poland; David F Butler, MD, Professor of Dermatology, Texas A&M University College of Medicine; Director, Division of Dermatology, Scott and White Clinic; Director Dermatology Residency Training Program, Scott and White Clinic; Edward F Chan, MD, Clinical Assistant Professor, Department of Dermatology, University of Pennsylvania School of Medicine; Catherine Quirk, MD, Clinical Assistant Professor, Department of Dermatology, Brown University; Dirk M Elston, MD, Director, Department of Dermatology, Geisinger Medical Center Author and Editor Disclosure Synonyms and related keywords: factitious disorder, Munchhausen's syndrome by proxy, Münchhausen syndrome by proxy, Munchhausen syndrome by proxy, acne excoriee, picker's nodules, picker nodules, psychocutaneous disease, psychosomatic dermatoses, self-injurious behaviors, obsessive-compulsive behavior, attention-seeking behavior, self injury, self-induced excoriations INTRODUCTIONBackgroundThe skin and nervous system develop adjacent to each other as the ectoderm and neuroectoderm, respectively, in the embryo and remain interconnected throughout life. Dermatitis artefacta is defined as the deliberate and conscious production of self-inflicted skin lesions to satisfy an unconscious psychological or emotional need. These skin lesions serve as powerful, self-expressive, nonverbal messages. Patients often deny responsibility for their creation. Neurotic excoriation is differentiated from dermatitis artefacta by its conscious compulsive nature. Dermatitis artefacta falls under the general category of factitious disorders, which excludes neurotic excoriations, delusional disorders, malingering, and Münchhausen syndrome (except Münchhausen syndrome by proxy). Psychiatric conditions, in particular depression, anxiety, personality disorders, delusional disorders, and dissociative disorders, are often coexistent in 25-33% of all dermatological conditions. Dermatitis artefacta may occur in persons of any age and commonly manifests within the context of chronic medical and/or dermatological conditions. These self-induced skin lesions may be present continuously, or they may be episodic, occurring during periods of heightened psychosocial stress and/or uncontrolled psychoses. Patients with dermatitis artefacta require both dermatological assessment and psychosocial support. PathophysiologyThe pathophysiology of dermatitis artefacta is poorly understood. Multifactorial causes include genetics, psychosocial factors, and personal or family history of psychiatric illness. Commonly, a family member is involved in the medical field, and patients tend to be well versed in medical terminology. Acute episodes often represent a maladaptive response to a psychosocial stressor. Long-standing cases may be secondary to underlying anxiety or depression, emotional deprivation, an unstable body image, or a personality disorder with borderline features. Many patients also have an associated chronic medical or dermatological condition. FrequencyInternationalThe prevalence in the pediatric population is 1 case in 23,000 persons. It is more common than is typically thought because it is poorly recognized and underreported. Mortality/MorbidityDermatitis artefacta is poorly recognized and underreported. Additionally, many patients are lost to follow-up.
RaceNo racial or ethnic predisposition has been noted. SexMost patients with dermatitis artefacta are females.
AgeThe highest incidence occurs between late adolescence (age 11-14 y) and early adulthood. CLINICALHistory
PhysicalDermatitis artefacta is a challenging clinical diagnosis. It is suggested based on findings that include an absence of other dermatoses to explain the lesions and histological findings that are inconsistent with the clinical presentation.
CausesThe cause is multifactorial. One should be sure to rule out hypochondriasis, substance abuse disorder, and psychotic disorders.
DIFFERENTIALSAlopecia Areata Anagen Effluvium Atopic Dermatitis Bedbug Bites Contact Dermatitis, Allergic Contact Dermatitis, Irritant Delusions of Parasitosis Friction Blisters Impetigo Insect Bites Neurotic Excoriations Onycholysis Prurigo Nodularis Pruritus and Systemic Disease Telogen Effluvium Trichotillomania
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| Drug Name | Bacitracin, Neomycin and Polymyxin B (AK-Spore Ointment, Neocin, Neosporin) |
|---|---|
| Description | Bacitracin prevents transfer of mucopeptides into growing cell wall, inhibiting bacterial growth. Neomycin is used for treatment of minor infections; inhibits bacterial protein synthesis and growth. Polymyxin B disrupts bacterial cytoplasmic membrane, permitting leakage of intracellular constituents and causing inhibition of bacterial growth. |
| Adult Dose | Apply 1-4 times/d to affected areas and cover with sterile bandages prn |
| Pediatric Dose | Administer as in adults |
| Contraindications | Documented hypersensitivity; epithelial herpes simplex keratitis; mycobacterial and fungal infections |
| Interactions | None reported |
| 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 | Caution when treating extensive burns (>20% BSA) because absorption of neomycin is possible and may cause nephrotoxicity and ototoxicity; prolonged use may result in overgrowth of nonsusceptible organisms |
| Drug Name | Fusidic acid (Fucidin, Fusidin, Fusidin Leo) |
|---|---|
| Description | Topical antibacterial that inhibits bacterial protein synthesis, causing bacterial death. |
| Adult Dose | Apply to affected area bid for 2 wk |
| Pediatric Dose | Administer as in adults |
| Contraindications | Documented hypersensitivity |
| Interactions | None reported |
| 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 | Discontinue if irritation or sensitivity occurs |
For impetiginized skin lesions.
| Drug Name | Cephalexin (Keflex, Keftab, Biocef) |
|---|---|
| Description | First-generation cephalosporin that inhibits bacterial replication by inhibiting bacterial cell wall synthesis. Bactericidal and effective against rapidly growing organisms forming cell walls. Resistance occurs by alteration of penicillin-binding proteins. Effective for treatment of infections caused by streptococci or staphylococci, including penicillinase-producing staphylococci. May use to initiate therapy when streptococcal or staphylococcal infection is suspected. Used orally when outpatient management is indicated. Recommended for impetigo caused by Staphylococcus aureus resistant to erythromycin. Primary activity against skin florae. Used for skin infections or prophylaxis in minor procedures. |
| Adult Dose | 500 mg PO q6h for 10 d |
| Pediatric Dose | 25-50 mg/kg/d PO q6h for 10 d; not to exceed 3 g/d |
| Contraindications | Documented hypersensitivity |
| Interactions | Coadministration with aminoglycosides increases nephrotoxic potential |
| Pregnancy | B - Fetal risk not confirmed in studies in humans but has been shown in some studies in animals |
| Precautions | Adjust dose in severe renal insufficiency (high doses may cause CNS toxicity); superinfections and promotion of nonsusceptible organisms may occur with prolonged use or repeated therapy |
| Drug Name | Erythromycin (E-Mycin, Eryc, Ery-Tab) |
|---|---|
| Description | Use with hypersensitivity or contraindication to penicillin or cephalexin. May result in GI upset, prompting prescription of an alternative macrolide or a change to tid dosing. Covers most potential etiologic agents, including Mycoplasma species. Less active against Haemophilus influenzae. Although 10 d seems to be a standard course of treatment, treating until patient has been afebrile for 3-5 d seems more rational. Inhibits bacterial growth, possibly by blocking dissociation of peptidyl tRNA from ribosomes, causing RNA-dependent protein synthesis to arrest. For treatment of staphylococcal and streptococcal infections. In children, age, weight, and severity of infection determine proper dosage. When bid dosing is desired, half the total daily dose may be taken q12h. For more severe infections, double the dose. Has added advantage of being a good anti-inflammatory agent by inhibiting migration of polymorphonuclear leukocytes. |
| Adult Dose | 250 mg erythromycin stearate/base (or 400 mg ethylsuccinate) PO q6h, or 500 mg q12h (1 h ac or 2 h pc) Alternatively, 333 mg PO q8h; increase to 4 g/d depending on severity of infection |
| Pediatric Dose | 30-50 mg/kg/d (base or ethylsuccinate) PO divided q6-8h; not to exceed 2 g/d (base) or 3.2 g/d (ethylsuccinate) |
| Contraindications | Documented hypersensitivity; hepatic impairment |
| Interactions | Coadministration may increase toxicity of theophylline, digoxin, carbamazepine, and cyclosporine; may potentiate anticoagulant effects of warfarin; coadministration with lovastatin and simvastatin increases risk of rhabdomyolysis; decreases metabolism of repaglinide, thus increasing serum levels and effects |
| Pregnancy | B - Fetal risk not confirmed in studies in humans but has been shown in some studies in animals |
| Precautions | Caution in liver disease; estolate formulation may cause cholestatic jaundice; adverse GI effects are common (give doses pc); discontinue use if nausea, vomiting, malaise, abdominal colic, or fever occurs |
First-line therapy for depression. Other medications in this category include paroxetine, citalopram, and sertraline. For dermatitis artefacta associated with obsessive-compulsive disorder, the use of an SSRI for at least 6 months to 1 year accompanied by psychotherapy is recommended.
| Drug Name | Fluoxetine (Prozac) |
|---|---|
| Description | Selectively inhibits presynaptic serotonin reuptake with minimal or no effect in reuptake of norepinephrine or dopamine. May cause more adverse GI effects than other SSRIs currently available, which is the reason it is not recommended as a first choice. May be given as a liquid and a cap. May give as single dose or in divided doses. Presence of food does not appreciably alter medication levels. May take up to 4-6 wk to achieve steady-state levels because of long half-life (72 h). Long half-life is both an advantage and a drawback. If it works well, an occasional missed dose is not a problem; if problems occur, eliminating all active metabolites takes a long time. Choice depends on adverse effects and drug interactions. Adverse effects of SSRIs seem to be quite idiosyncratic; thus, if dosing is started at a conservative level and advanced as tolerated, relatively few reasons exist to recommend one over another. |
| Adult Dose | 20 mg/d PO in morning and increase after several wk by 20 mg/d; not to exceed 80 mg/d Note: If patient is taking 20 mg/d, may initiate once-weekly dosing with 90-mg delayed-release product 7 d after last daily dose of 20 mg |
| Pediatric Dose | <8 years: Not established >8 years: 10-20 mg PO qd |
| Contraindications | Documented hypersensitivity; concurrently taking MAOIs or took them in last 2 wk; coadministration with thioridazine |
| Interactions | Increases toxicity of diazepam and trazodone by decreasing clearance; also increases toxicity of MAOIs and highly protein-bound drugs; serotonin syndrome (ie, myoclonus, rigidity, confusion, nausea, hyperthermia, autonomic instability, coma, eventual death) occurs with simultaneous use of other serotonergic agents (eg, anorectic agents, tramadol, buspirone, trazodone, clomipramine, nefazodone, tryptophan); discontinue other serotonergic agents at least 2 wk prior to SSRI initiation |
| Pregnancy | B - Fetal risk not confirmed in studies in humans but has been shown in some studies in animals |
| Precautions | Caution in hepatic impairment and history of seizures; discontinue MAOIs at least 14 d before initiating therapy |
| Drug Name | Doxepin (Sinequan, Zonalon) |
|---|---|
| Description | Has antihistamine, antipruritic, and antidepressant properties. May be effective for depression (with agitation) and a primary symptom of pruritus. Increases concentration of serotonin and norepinephrine in CNS by inhibiting their reuptake by presynaptic neuronal membrane, which is associated with a decrease in symptoms of depression. |
| Adult Dose | 30-150 mg/d PO hs or 2-3 divided doses; gradually increase dose to 300 mg/d prn; maintain effective dose for at least 6-8 wk |
| Pediatric Dose | <12 years: Not recommended >12 years: 25-50 mg/d PO hs or bid/tid and increase gradually to 100 mg/d |
| Contraindications | Documented hypersensitivity; urinary retention; acute recovery phase following myocardial infarction; glaucoma |
| Interactions | Decreases antihypertensive effects of clonidine but increases effects of sympathomimetics and benzodiazepines; effects of desipramine increase with phenytoin, carbamazepine, and barbiturates |
| 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 | Caution in cardiovascular disease, conduction disturbances, seizure disorders, urinary retention, hyperthyroidism, and thyroid replacement therapy |
| Drug Name | Amitriptyline (Elavil, Endep) |
|---|---|
| Description | May be effective for depression with primary symptoms of pain sensations (eg, burning, chafing, stinging). Analgesia usually requires doses <50 mg qhs. Inhibits reuptake of serotonin and/or norepinephrine at presynaptic neuronal membrane, which increases concentration in CNS. May increase or prolong neuronal activity because reuptake of these biogenic amines is important physiologically in terminating transmitting activity. |
| Adult Dose | 25-150 mg/d mg PO hs; use minimum effective dose |
| Pediatric Dose | Children: 0.1 mg/kg PO hs; increase as tolerated over 2-3 wk to 0.5-2 mg/d hs Adolescents: 25-50 mg/d PO initially; increase gradually to 100 mg/d in divided doses |
| Contraindications | Documented hypersensitivity; use of MAOIs within 14 d of initiating therapy; history of seizures, cardiac arrhythmias, glaucoma, or urinary retention |
| Interactions | Phenobarbital may decrease effects; coadministration with CYP2D6 enzyme system inhibitors (eg, cimetidine, quinidine) may increase levels; inhibits hypotensive effects of guanethidine; may interact with thyroid medications, alcohol, CNS depressants, barbiturates, and disulfiram |
| 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 | Caution in cardiac conduction disturbances and history of hyperthyroidism, renal, impairment, or hepatic impairment; avoid use in elderly persons |
| Drug Name | Pimozide (Orap) |
|---|---|
| Description | Previously shown to be effective for delusions of parasitosis. Centrally acting dopamine-receptor antagonist. Available in 2-mg scored tab in United States; 2-, 4-, and 10-mg tab available in Canada. Clinical response usually occurs within 10-14 d. |
| Adult Dose | 1-2 mg PO qd initially; increase by 2-4 mg at weekly intervals; not to exceed 10 mg/d or 200 mcg/kg/d (0.2 mg/kg/d); maintain effective therapeutic dose for at least 1 mo and then titrate down in 1-mg decrements over 1-2 wk until minimum effective dose is achieved |
| Pediatric Dose | Not established |
| Contraindications | Documented hypersensitivity; history of cardiac arrhythmias or long QT syndrome; concurrently with macrolide antibiotics |
| Interactions | Increases toxicity of MAOIs, alfentanil, CNS depressants, and guanabenz |
| 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 | ECG recommended at initiation of therapy and regular intervals thereafter; careful observation for appearance of extrapyramidal symptoms (eg, akathisia, rigidity, dystonia, irreversible tardive kinesia) necessary in geriatric patients; adverse effect of restlessness (akathisia) may be treated with diphenhydramine or benztropine |
Lower risk of extrapyramidal adverse effects than with typical antipsychotics.
| Drug Name | Risperidone (Risperdal) |
|---|---|
| Description | Previously shown to be effective for delusions of parasitosis. Binds to dopamine D2 receptor with 20-times lower affinity than for 5-HT2 receptor. Improves negative symptoms of psychoses and reduces prevalence of extrapyramidal adverse effects. Indicated for treatment of psychotic disorders, including schizophrenia and bipolar disorder. Clinical response usually occurs within 10-14 d. |
| Adult Dose | 2-6 mg PO qhs; start at 0.5 or 1 qhs; may divide into bid dosing |
| Pediatric Dose | <16 years: Not recommended >16 years: 0.5-1 mg PO bid; not to exceed 6 mg/d |
| Contraindications | Documented hypersensitivity. |
| Interactions | Coadministration with carbamazepine may decrease effects; may inhibit effects of levodopa; clozapine may increase levels; oral solution not compatible with cola or tea |
| 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 | May cause extrapyramidal reactions, hypotension, tachycardia, and arrhythmias; hyperglycemia may occur and, in some cases, be extreme, resulting in ketoacidosis, hyperosmolar coma, or death; do not split or chew oral disintegrating tab |
| Drug Name | Olanzapine (Zyprexa) |
|---|---|
| Description | May inhibit serotonin, muscarinic, and dopamine effects. Efficacy similar to risperidone; has fewer dose-dependent adverse effects but is associated with more concern about weight gain. |
| Adult Dose | 5-20 mg/d PO in divided doses; lower doses recommended for dermatology-related psychoses |
| Pediatric Dose | Children: Not established Adolescents: Administer as in adults |
| Contraindications | Documented hypersensitivity |
| Interactions | Fluvoxamine may increase effects; antihypertensives may increase risk of hypotension and orthostatic hypotension; levodopa, pergolide, bromocriptine, charcoal, carbamazepine, omeprazole, rifampin, and cigarette smoking may decrease effects |
| 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 | Caution in narrow-angle glaucoma, cardiovascular disease, cerebrovascular disease, prostatic hypertrophy, seizure disorders, hypovolemia, and dehydration; hyperglycemia may occur and in some cases be extreme, resulting in ketoacidosis, hyperosmolar coma, or death; administration of more than 1 IM injection is associated with substantial orthostatic hypotension (33%), thus, maintain patient in recumbent position and monitor blood pressure before repeating IM doses |
| Drug Name | Quetiapine (Seroquel) |
|---|---|
| Description | May act by antagonizing dopamine and serotonin effects. Efficacy similar to risperidone and olanzapine. Fewer dose-dependent adverse effects and less concern for weight gain. |
| Adult Dose | 25 mg PO bid; titrate to 150-750 mg/d PO; not to exceed 800 mg/d; lower doses recommended for dermatology-related psychoses |
| Pediatric Dose | Children: Not established Adolescents: Administer as in adults |
| Contraindications | Documented hypersensitivity |
| Interactions | May antagonize levodopa and dopamine agonists; phenytoin, thioridazine, and other liver enzyme inducers may reduce levels; CYP4503A inhibitors (eg, ketoconazole, fluconazole, erythromycin) increase serum concentrations |
| 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 | May induce orthostatic hypotension associated with dizziness, tachycardia, and syncope; neuroleptic malignant syndrome and tardive dyskinesia have been associated with this treatment; hyperglycemia may occur and, in some cases, be extreme, resulting in ketoacidosis, hyperosmolar coma, or death; caution in hepatic impairment (decrease dose) |
Article Last Updated: Aug 24, 2007