Abstract
The nervous system and the skin develop next to each other in the embryo and remain intimately interconnected and interactive throughout life. The nervous system can influence skin conditions through psychoneuroimmunoendocrine mechanisms and through behaviors. Understanding the pathophysiology aids in selection of treatment plans for correcting the negative effects of the psyche on specific skin conditions. Medication options include standard psychotropic medications and alternative herbs and supplements. Other options include biofeedback, cognitive-behavioral methods, hypnosis, meditation, progressive relaxation, the placebo effect, and suggestion. When simple measures fail, combining medications with other therapeutic options may produce better results. Skin conditions that have strong psychophysiologic aspects may respond well to techniques such as biofeedback, cognitive-behavioral methods, hypnosis, meditation, or progressive relaxation that help to counteract stress. Treatment of primary psychiatric disorders that negatively influence skin conditions often results in improvement of those skin conditions. Abnormal conditions of the skin, hair, and nails can also influence the psyche negatively. Treatment of secondary psychiatric disorders such as anxiety or depression that are triggered or exacerbated by the appearance of these skin conditions or the associated discomfort may also be required.
Keywords: psychodermatology, psychosomatic, psychocutaneous, skin disorders, treatment, standard, alternative, non-drug
Overview of psychocutaneous disorders
The nervous system and the skin begin to form and develop side by side in the top layer or ectoderm of the fetus and remain intimately interconnected and interactive throughout life. The neural receptors in the skin may be viewed as the largest sense organ of the body and are key to skin protection and health. Many skin disorders have a significant psychosomatic or behavioral element.1 Nervous system-skin interactions allow drug and non-drug psychotherapeutic interventions that produce positive effects on many cutaneous diseases. These effects occur through actions of drugs, the autonomic nervous system, local hormones, and neuropeptides, resulting in neurogenic modulation of cutaneous inflammation.2 The skin is also affected by brain-regulated behavioral habits which alter exposure to various environmental factors such as sun exposure, and occupational and recreational exposures to animals, plants, and chemicals, and climate changes associated with travel. Skin disorders often have negative effects on the patient’s psychological and social status. Drug and non-drug interventions may help ameliorate the negative effects of the skin disorder on the psyche.3 A combined approach using both drug and non-drug methods is often needed when treating complex cutaneous psychosomatic and somatopsychosocial problems. Patients who are referred by a dermatologist or family physician to a psychiatrist or psychologist often refuse the referral or fail to keep the appointment. Few dermatologists are adequately cross-trained in psychiatry or psychology. A recent review of psychodermatology covered the relevant literature from 1951 to 2004.4 The development of subspecialty training in psychodermatology is currently being considered.5 How important the psychosocial aspects of skin, hair, and nails are to many individuals is reflected in the large amount of money spent on skin, hair, and nail products, and on cosmetic skin procedures.
Skin disorders with psychophysiologic aspects
Stress and emotion
Inflammatory and sensory skin disorders are significantly influenced by stress and emotion. Griesemer, who trained both as a dermatologist and as a psychiatrist, estimated the effect that emotions had on skin disease for each patient he saw during one year in his practice. From these data he developed an index6 of the effects of emotions on specific skin disorders.7 The pathways by which stress and emotion affect the nervous system, immune system, and hormonal system and their subsequent effects on inflammation and autonomic functioning and on the skin are still being elucidated. 8 Stress can induce or exacerbate anxiety disorders or depression in susceptible individuals. Drugs that reduce anxiety or depression can be helpful in those individuals. No direct anti-stress drug had yet been developed. The non-drug modalities of relaxation, biofeedback, meditation, or self-hypnosis can counteract stress and emotion.9 Simple inexpensive temperature-sensitive stress cards can be used to promote hand warming, which is associated with relaxation.10 Heart rate variability (HRV) biofeedback accompanied by slower deeper breathing can also reduce the effects of stress and emotion.11 Compact, highly portable, handheld HRV biofeedback devices such as the HeartMath emWave® personal stress reliever and the StressEraser® have recently become available.
Stress and emotion reduction in skin conditions
Inflammatory, immune-mediated, and behavioral skin disorders are influenced by psychosomatic factors.12 In a recent study, 10% of patients at a dermatology clinic had psychosomatic disorders and another 15% had adjustment disorders.13 In conjunction with other appropriate treatments for the skin disorders, reducing stress, emotions, and behavioral habits that impair healing or damage to skin, hair, or nails can enhance response to treatment. Associated anxiety or depression can be treated with anxiolytic drugs or antidepressants.14 Non-drug methods of stress reduction such as relaxation, meditation, self-hypnosis, physical exercise, or biofeedback can directly counteract the stress.
Acne
Acne vulgaris often flares with stress and premenstrually.15 With worsening of the acne, many individuals get more stressed, setting up a vicious cycle. Conventional acne treatments can help control the acne, reducing the patient’s stress about having the acne. Stress may also be lessened with relaxation training 16 or another of the above-mentioned methods.
Alopecia areata
Alopecia areata usually occurs as patchy bald spots where immune dysregulation results in the hair follicles being attacked by inflammatory T-lymphocytes. Alexithymia with difficulty recognizing and describing feelings and dissociative somatization has been reported to be more common in adults with alopecia areata than in controls.17 Stress can initiate or worsen alopecia areata.18 The hair loss can aggravate the stress, especially if the hair loss is visible to others. Self-image issues and stress may be treated with self-hypnosis19 or another of the aforementioned methods.
Atopic dermatitis
Atopic dermatitis is produced mainly by scratching and flares with stress though psychoneuroimmunomechanisms. 20 Worsening atopic dermatitis can further stress the patient, who then tends to scratch more and further worsen the dermatitis. Stress may be lessened with cognitive-behavioral methods,21 hypnosis or self-hypnosis,22 or another of the above-mentioned methods. If indicated, adjunctive anxiolytic drugs or antidepressants may be employed.
Dermatitis artifacta
Self-induced factitial damage to the skin often occurs in odd otherwise unexplainable forms and may indicate a seriously disturbed patient or may occur for secondary gain.23 Consultation with a psychiatrist or psychologist is recommended. Often the patient denies self-inflicting the trauma and frequently is noncompliant in obtaining a psychiatric evaluation.
Dyshidrosis
Dyshidrosis consisting of tiny blisters on palms and/or soles typically flares with stress.6 In addition to conventional topical treatments, stress reduction can be of benefit. Stress may be reduced by HRV biofeedback, or galvanic skin response (GSR) biofeedback24 or another of the above-mentioned methods.
Erythema nodosum
Erythema nodosum with deep painful red nodules on the legs may worsen with stress. The author has reported a case of resolution of intractable erythema nodosum following hypnoanalysis.25
Herpes simplex
Stress frequently initiates or exacerbates herpes simplex cold sore virus recurrences.26 Along with using conventional antiviral treatments for the herpes, stress reduction may be facilitated with self-hypnosis27 or another of the aforementioned methods.
Hyperhidrosis
Hyperhidrosis of hands, feet, axillae, or forehead has a clear rapid onset correlation with stress.6 Locally injected botulinum toxin (Botox®) can temporarily inactivate acetylcholine release from the nerves associated with sweating.28 Stress may be reduced with GSR biofeedback, or HRV biofeedback29 or another of the above-mentioned methods.
Lichen planus
Lichen planus, an inflammatory pruritic dermatosis, is often triggered or exacerbated by stress. The intense itching and discoloration with hyperpigmentation that typically occur with lichen planus can further fuel the stress. As an indicator of stress, elevated salivary cortisol levels have been detected in patients with oral lichen planus.30 The stress may be reduced using self-hypnosis27 or another of the aforementioned methods.
Lichen simplex chronicus
Thickened plaques of lichen simplex chronicus are produced by rubbing or scratching the skin and are initiated or exacerbated by stress. In some cases, dissociation with somatization may play a role.31 Along with standard topical treatments, stress reduction can be beneficial. The stress may be reduced with self-hypnosis27 or another of the above- mentioned methods.
Neurotic excoriations
Neurotic excoriations are skin damage self-induced by scratching,32 and neurotic or psychogenic excoriations are worsened by stress. The stress may be lessened with self-hypnosis33 or another of the aforementioned methods. The commonly associated anxiety or depression may be treated with adjunctive anxiolytic drugs or antidepressants.
Nummular dermatitis
Nummular dermatitis consists of coin-shaped patches on dry areas of skin and in some individuals can flare with stress. Connections of nerves to mast cells have been noted in the basement membrane zone in nummular dermatitis.34 Along with standard topical treatments, stress reduction can be helpful. The stress may be reduced using self-hypnosis27 or another of the above-mentioned methods.
Perioral dermatitis
Perioral dermatitis, similar to acne but located around the mouth, can be exacerbated by stress or other neurogenic factors.35 Along with conventional topical treatments, stress reduction can be useful. The stress may be reduced with self-hypnosis27 or another of the aforementioned methods.
Pruritus
Pruritus or itching is frequently worsened by stress. Many inflammatory skin diseases are itchy via neuroimmunoendocrine mechanisms.36 See later under neurogenic cutaneous sensory dysesthesias for further discussion of pruritus and its treatment. Stress reduction can be helpful. The stress may be lessened with self-hypnosis27 or another of the above-mentioned methods.
Psoriasis
Psoriasis in many patients flares with stress.37 Along with standard treatments, stress reduction can help reduce flares. Many patients are distressed by the disfigurement of the skin by the psoriatic lesions. Alexithymia with dissociative somatization can aggravate psoriasis and has a higher risk of associated alcoholism.38 Body image issues and stress and may be improved with cognitive-behavioral methods,39 biofeedback, meditation,40 relaxation training, or self-hypnosis.41
Rosacea
With rosacea the facial flushing and the papular inflammations both can flare with stress.42 Many rosacea patients are in turn distressed by their facial appearance. Stress may be reduced with self-hypnosis27 or another of the above-mentioned methods.
Seborrheic dermatitis
Stress frequently worsens the scaling and itching of seborrheic dermatitis.36 In addition to conventional treatments for the seborrheic dermatitis, stress may be reduced using self-hypnosis27 or another of the aforementioned methods.
Telogen effluvium
Telogen effluvium is diffuse hair loss and may be acute or chronic. Common initiators are stress, low protein intake, and hormonal changes.43 Stress may be reduced with one of the above mentioned methods. Any accompanying depression may be treated with an antidepressant.14
Trichotillomania
Stress can worsen the repetitive pulling and twisting behavior that produces trichotillomania.44 Reducing stress may be accomplished with self-hypnosis45 or another of the aforementioned methods.
Urticaria
Urticaria or hives may be triggered or exacerbated by stress.36 The itchy urticaria can in itself be stressful, creating a vicious circle. Stress may be reduced with self-hypnosis46 or another of the above-mentioned methods.
Influence of primary psychiatric disorders on skin diseases
Primary anxiety
Acute or chronic anxiety can worsen many skin disorders. Having a skin disorder can also induce anxiety in susceptible individuals. In a recent study, 13% of patients seen at a dermatology clinic had an anxiety disorder.13
Psychogenic pruritus
Psychogenic pruritus or itching initiated or exacerbated by anxiety or psychological trauma or stress should be considered when other causes of pruritus have been ruled out.34 Stress and anxiety may be lessened using self-hypnosis27 or another of the above-mentioned methods. Anxiety may also be treated with anxiolytics.14
Delusions
Delusions of parasitosis
Delusions of parasitosis occur when the patient insists that they have bugs growing in or on their skin when objectively they do not. This is one of the monomaniacal delusions. Compliant patients generally respond to typical antipsychotics such as pimozide or atypical antipsychotics such as olanzapine or risperidone. Parenterally administered risperidone was found to be particularly effective, since this route of administration had built-in monitoring of compliance.47
Primary depression
Depression and risk of self-harm or suicide can occur as a primary process or secondary to a skin disease. Primary depression may also be associated with acts that self-harm the skin such as scratching, picking, digging, burning, cutting, pulling, tearing, or otherwise harming the skin, hair, or nails.48 In a recent study, 32% of patients seen at a dermatology clinic had depression.13 The majority of patients who have self-inflicted dermatoses such as neurotic or psychogenic excoriations suffer from depression with somatization.49 Treating the depression with an antidepressant14 may help to reduce or eliminate the self-damaging habit.
Impulse control
Acne excoriée
Some patients who pick at their acne excessively are primarily impulsive in their picking. Along with standard treatments for the acne, reducing or stopping the picking habit is necessary. Cognitive–behavioral methods or hypnosis and self-hypnosis50 may be used. If these measures fail, hypnoanalysis may be considered.
Neurodermatitis
Some neurodermatitis patients are primarily impulsive in their picking.51 Cognitive–behavioral methods52 or hypnosis and self-hypnosis27 may be of benefit. For resistant cases, hypnoanalysis may be employed.
Trichotillomania
Trichotillomania is currently classified as an impulse control disorder.44 Cognitive-behavioral methods may be beneficial.53 Hypnoanalysis may help deal with root causes in refractory cases.
Obsessive–compulsive disorder
Obsessive–compulsive disorder spectrum patterns may be a primary factor in producing skin disease or in exacerbating a pre-existing skin disease such as acne, atopic dermatitis, or psoriasis. In a recent study, about 5% of patients evaluated at a dermatology clinic had obsessive–compulsive disorder.13
Acne excoriée
Some acne excoriators are primarily obsessive–compulsive in their picking.50 Cognitive-behavioral methods may be helpful, as may selective serotonin reuptake inhibitor (SSRI) antidepressants.54 Hypnosis with pattern-interrupt suggestions may also be of benefit.
Onychotillomania
Onychotillomania is compulsive manipulation causing damage to nails. It may be a form of obsessive–compulsive disorder. 55 Cognitive-behavioral methods may be of benefit, as may SSRI antidepressants.54 Hypnosis with pattern-interrupt suggestions may also help.
Neurodermatitis
Some patients with neurodermatitis or psychogenic excoriations fit best into the obsessive–compulsive category.49 Cognitive-behavioral methods may be of benefit, as may SSRI antidepressants.54 In some patients, hypnosis with pattern-interrupt suggestions may be effective. In unresponsive cases, hypnoanalysis may be considered.
Somatization with dissociation
Unexplainable bodily symptoms that have no underlying physical pathology are common both in general medicine and in dermatology. Common somatization with dissociation syndromes in general medicine include chronic fatigue syndrome, fibromyalgia, irritable bowel syndrome, and interstitial cystitis.56 In dermatology, somatization with dissociation syndromes include unexplained cutaneous sensory syndromes (see below), body memories from traumatic stress in post traumatic stress syndrome (PTSD) that manifest as pruritus, urticaria, or angioedema, self-induced dermatitis artifacta and trichotillomania associated with dissociative states, and body dysmorphic disorder, where the patient has a distorted somatic preoccupation involving the skin or hair.49 Among acne patients, 14% to 21% have aspects of body dysmorphic disorder.57 Nihilodermia refers to problem patients without objective skin findings but who have recurrent symptoms and are insistent on medical examination and treatment.58 Alexithymia is associated with somatization with dissociation and is characterized by difficulty in recognizing and describing feelings.59 As a general rule, functional somatic syndromes seem more responsive to active non-drug treatments requiring active patient participation, such as exercise and psychotherapy compared with passive physical procedures and injections. Also, drugs that have a central nervous system action generally are more effective than those that affect peripheral physiologic function. 60 If antidepressant treatment alone is ineffective, adding pregabalin may result in improvement.61
Neurogenic cutaneous sensory dysesthesias
Dysesthesias arising in the central nervous system
Generalized pruritus or itching without any visible skin eruption can be due to metabolic, renal, thyroid, hematologic, and other internal diseases. After ruling these out, central nervous system dysfunction as the source of neurogenic pruritus should be considered. One example is pruritus associated with neurotic excoriations.62 Another example is otherwise unexplained pruritus associated with somatization with dissociation. 63 Sedating antihistamines such as hydroxyzine or doxepin have some antipruritic effect, as may some opiate agonists, but for neurogenic pruritus there is no really potent antipruritic drug.
Dysesthesias arising in the peripheral nervous system
Brachioradial pruritus
Brachioradial pruritus or itching of the arm, antecubital fossa, and proximal forearm tends to occur in lightly pigmented individuals who have had extensive chronic sun exposure.64 This generally is more prominent during the summer. In some patients, peripheral neuropathic pruritus associated with cervical spinal foramen nerve impingement may be the etiologic factor.65 Relief from the pruritus may be obtained by sun protection, topical menthol, topical capsaicin, or oral gabapentin.
Glossodynia
After organic factors for tongue pain such as vitamin deficiency are ruled out, treatment of glossodynia is symptomatic with topical anesthetics. In some cases, oral gabapentin or oral olanzapine may be useful.66
Notalgia paresthetica
Notalgia paresthetica is a peripheral neuropathic pruritus of the medial subscapular shoulder blade area that, at least in some cases, may relate to nerve impingement in a thoracic spinal foramen.67 The topical antipruritics, menthol or capsaicin, may offer relief, as may oral gabapentin.67
Postherpetic neuralgia
Postherpetic neuralgia is a peripheral neuropathic pruritus, pain, or paraesthesia following herpes zoster (shingles). It occurs more frequently in individuals older that 60. Topical treatment with capsaicin four or five times a day, which depletes substance P in the nerves, may be useful. Oral gabapentin also may help reduce the neuropathic sensations. 68 Acupuncture and hypnosis27 for pain or pruritus have provided relief in some patients.
Pruritus ani, pruritus scroti, and pruritus vulvae
Organic factors such as pinworms, candidal and fungal infections, and inflammatory skin diseases should be ruled out first. The source of the pruritus ani, pruritus scroti, or pruritus vulvae may be peripheral neuropathic as a result of sacral nerve impingement69 or may be psychogenic. Topical pramoxine and hydrocortisone may offer relief for some patients. Oral antihistamines may benefit some patients.70
Secondary psychiatric disorders associated with skin diseases
Around 30% of patients with skin disorders are reported to have psychiatric disorders and psychosocial impairments.71 The overall prevalence of psychological disorders among patients with skin disease is about 25% to 30%, but even higher prevalence rates, above 30%, occur among patients with acne, alopecia, herpes simplex pruritus, and urticaria.72 Skin disease with associated psychological morbidity results in poorer quality of life than just having the skin disease alone.73
Secondary anxiety
Acne
In susceptible individuals, acne can lower self-esteem, self-confidence, cause embarrassment, and impair social functioning. In anxiety-prone individuals, acne can also increase anxiety substantially. The added stress and anxiety can cause acne to flare, creating a vicious cycle.74 Drug treatments for anxiety include a low-dose benzodiazepine monitored carefully, buspirone, or herbal anxiolytics, such as magnolia bark or passion flower. Relaxation techniques, self-hypnosis, or biofeedback for relaxation can enhance treatment of anxiety without the side effects of drugs.
Urticaria
Urticaria or hives with release of pruritus-inducing histamine can induce anxiety in anxiety-prone individuals. The anxiety can in turn flare the urticaria, creating a vicious cycle.36 The antihistamines diphenhydramine, doxepin, and hydroxyzine are sedating and can reduce anxiety while also reducing the urticaria through their antihistaminic effect.
Secondary depression
For each of the conditions below, patients with major depression should be referred to a psychiatrist for care. SSRIs or tricyclics may be prescribed for minor depression,14 or the herb St. John’s wort may be recommended. Cognitive-behavioral therapy may also be helpful for depression.
Acne
Acne usually begins in puberty in conjunction with sex hormone changes. Adolescent patients with severe acne had a prevalence of depression of about 18% to 29%, compared with a prevalence of depression of about 5% to 8% for the general adolescent population.75 Depressive symptoms are often concealed, denied or expressed through aggressive or disruptive behavior in adolescents. A more severe form of acne, nodulocystic acne, often persists late into adulthood. Oral isotretinoin used to treat nodulocystic acne has been questionably associated with increased depression and suicide.76
Alopecia
Hair loss may occur with androgenetic (male pattern) alopecia, alopecia areata (patchy hair loss), scarring from discoid lupus or lichen planopilaris, telogen effluvium (diffuse hair loss), hypothyroidism, as a side effects of drugs, especially cancer chemotherapy drugs, or as a result of behavior such as trichotillomania or traction alopecia. Hair appearance can affect psychosocial functioning. In susceptible individuals, hair loss can induce or exacerbate depression. Alopecia areata can worsen with depression.16
Atopic dermatitis
The pruritus or itching of atopic dermatitis can aggravate depression in depression-prone individuals, who then often scratch more and worsen their skin disorder.77 The antihistamines diphenhydramine, hydroxyzine, and doxepin cause sedation and can reduce pruritus and scratching through their antihistaminic effect. Doxepin is also a tricyclic antidepressant. Individuals with major depression should be referred to a psychiatrist for care. Self-hypnosis with suggestions for soothing can reduce pruritus or itching and give the patient a sense of greater control, which in turn can improve the depression.
Disfigurement
Disfigurement secondary to skin disorders, traumatic injuries, 78 and surgeries for skin cancers can aggravate depression in depression-prone individuals. Hypnosis and reframing can alter the patient’s perspective on their disfigurement, secondarily reducing depression.
Malignant melanoma
Metastatic melanoma often has a grim prognosis and can induce situational depression, which in turn degrades the body’s immune response79 against the melanoma metastases. Treatment of the depression may enhance the body’s ability to respond against the melanoma.
Psoriasis
In depression-prone individuals, psoriasis can initiate or exacerbate depression, which in turn can enhance the sensation of pruritus.77 Injuring the skin by scratching psoriatic plaques can exacerbate the psoriasis. Self-hypnosis can reduce pruritus or itching and give a sense of greater self-control, which in turn can lessen the depression.
Urticaria
In depression-prone individuals, chronic urticaria can initiate or exacerbate depression which can in turn exacerbate pruritus.77 Self-hypnosis can reduce pruritus or itching and give a sense of greater self-control, which can lessen the depression. Hypnosis has resolved some cases of chronic urticaria.25
Vitiligo
In depression-prone individuals, vitiligo can initiate or exacerbate depression, especially in darkly pigmented individuals. 80 The prevalence of depression in vitiligo patients was 39% in a recent quality of life study.81 Cognitive-behavioral therapy may help reduce the depression.82 Hypnosis can also help to reframe the patient’s perspective on their depigmented lesions, lessening secondary depression.
Therapeutic options
Conventional pharmacologic psychocutaneous therapies
For the most current information on specific products, check the current Physicians’ Desk Reference,83 package inserts, or other appropriate information source to ascertain dosages, indications and usage, review pharmacokinetics, and note contraindications, warnings, precautions, drug interactions, and adverse reactions. Many psychotropic drugs should be started at a low dose and progressively increased to therapeutic range, then tapered as appropriate. 14 Dosages given in the tables are for the average healthy young or middle-aged adult. Lower initial dosages are recommended in the elderly because of slower renal and/or hepatic clearance.
Antidepressants
SSRIs are used in dermatology to treat depression, anxiety, and obsessive–compulsive spectrum disorders associated with skin diseases. Side effects of SSRIs include nausea, diarrhea, insomnia, or sedation.14 SSRIs should be started at low dose and titrated upward. Onset of effects of SSRIs is slow, usually taking three to six weeks (see Table 1).
Table 1.
Category | Agent | Dosage | Side effects | Cautions |
---|---|---|---|---|
SSRI | Citalopram (Celexa®) | 20–40 mg daily | Sedation | SSRIs slow |
Escitalopram (Lexapro®) | 10 mg daily | onset of effect | ||
Fluoxetine (Prozac®) | 20–80 mg daily | Insomnia | Taper off slowly | |
Fluvoxamine (Luvox®) | 25–150 mg bid | GI symptoms | Multiple drug | |
Paroxetine (Paxil®) | 20–50 mg daily | Sedation | Interactions | |
Sertraline (Zoloft®) | 25–200 mg daily | GI symptoms | ||
Venlafaxine (Effexor®) | 25–75 mg tid | |||
Tricyclic | Amitriptyline (Elavil®) | 25–50 mg daily | Sedation, dry mouth | Tricyclics |
Clomipramine (Anafranil®) | 25–250 mg daily | Sedation, dry mouth | Risk of seizures | |
Doxepin (Sinequan®) | 25–300 mg daily | Sedation | ||
Imipramine (Tofranil®) | 25–300 mg daily | Orthostatic hypotension | Heart dysconduction | |
Nortriptyline (Pamelor®) | 25–150 mg daily | Dry mouth | ||
Protryptyline (Vivactil®) | 5–20 mg tid | Dry mouth | ||
Trimipramine (Surmontil®) | 5–50 mg tid | Sedation | ||
NE/DUI | Bupropion (Welbutrin®) | 75–150 mg bid | ||
Herbs | St. John’s wort | 300–1200 mg daily | Photosensitivity | Drug interactions |
Supplement | SAMe | 200–800 mg bid | ||
Non-drug | Exercise | Daily | ||
Hypnosis | Daily |
Abbreviations: bid, twice daily; GI, gastrointestinal; SSRI, selective serotonin reuptake inhibitor; NE/DUI, norepinephrine and dopamine reuptake inhibitor; SAMe, S-adenosul-L-methionine; tid, three times daily.
Tricylic antidepressants are also used in dermatology for depression and obsessive–compulsive spectrum disorders (see Table 1). Doxepin, which also has antihistaminic properties, is the tricyclic most commonly prescribed by dermatologists. The norepinephrine and dopamine reuptake inhibitor bupropion, an aminoketone antidepressant, is less commonly used (see Table 1).
Antipsychotics
Typical (dopamine receptor antagonist) antipsychotics are used in dermatology for delusional psychoses such as delusions of parasitosis, delusions of bromhidrosis, and Morgellons delusions of fibers (see Table 2). Atypical (serotonin-dopamine antagonist) antipsychotics are often used in dermatology for treatment of resistant cases of obsessive–compulsive spectrum disorders, as a second agent in addition to SSRIs (see Table 2).
Table 2.
Category | Agent | Dosage | Side effects | Cautions |
---|---|---|---|---|
Antipsychotics | ||||
Typical | Haloperidol (Haldol®) | 5–20 mg daily acutely Maintenance 1–10 mg daily |
Tardive dyskinesia | Mild sedation |
Pimozide (Orap®) | 0.5–10 mg daily acutely Maintenance 0.5–5 mg daily |
Tardive dyskinesia | ||
Atypical | Olanzapine (Zyprexa®) Risperidone (Risperdal®) Ziprasidone (Geodon®) |
2.5–10 mg daily 1–3 mg daily 20–100 mg bid |
Weight gain | Diabetes |
Anticonvulsants | ||||
GABA | Gabapentin (Neurontin®) Pregabalin (Lyrica®) |
100–600 mg tid 50–100 mg tid |
Abbreviations: bid, twice daily; GABA, gamma amino butyric acid; tid, three times daily.
Anticonvulsants
Gamma aminobutyric acid (GABA) elevators are used in dermatology for relief of pain, itching, or paraesthesias in peripheral neuropathies including postherpetic neuralgia (see Table 2).
Anxiolytics
Benzodiazapines are Schedule IV controlled substances because of their potential for abuse and addictive dependence. They tend to be sedating. In dermatology, they are used for pre-procedure anxiety. Generally the short-acting benzodiazapines are preferable for this purpose (see Table 3).
Table 3.
Category | Agent | Dosage | Side effects | Cautions |
---|---|---|---|---|
Benzodiazepines | Alazopram (Xanax) | 0.25–0.5 mg tid | Short-acting sedation | Use caution |
Lorazepam (Ativan) | 1 mg bid–tid | Short-acting sedation | Driving | |
Diazepam (Valium) | 2–10 mg bid–qid | Long-acting sedation | With each | |
Azaperone | Buspirone (Buspar) | 5–30 mg bid | Very slow acting | |
Herbs | Magnolia bark | 250–750 mg daily | ||
Passion flower | 0.5 1 ml fluid extract Daily–tid |
|||
Non-drug | Biofeedback | Daily and prn | ||
Cognitive-behavioral | Daily | |||
Hypnosis | Daily and prn | Avoid use driving | ||
Meditation | Daily and prn | Avoid use driving | ||
Placebo | Prn | |||
Suggestion | Prn | |||
Yoga | Daily and prn |
Abbreviations: bid, twice daily; Prn, per required need; tid, three times daily.
The serotonin agonist buspirone is an azaperone. Its advantages are that it is not a controlled substance and is nonsedating. Its disadvantage is that it has a delayed onset of action of about two weeks (see Table 3).
Sedatives
Sedating antihistamines are used extensively in dermatology for pruritus, angioedema, dermatographism, and urticaria. Hydroxyzine and promethazine are also mildly to moderately anxiolytic. In addition, doxepin has antidepressant properties (see Table 4).
Table 4.
Category | Agent | Dosage | Side effects | Cautions |
---|---|---|---|---|
Antihistamines | Certirizine (Zyrtec®) | 10 mg daily | Sedative | Use caution driving |
Diphenhydramine (Benadryl®) | 25–50 mg tid–qid | Sedative | With each | |
Doxepin (Sinequan®) | 25–100 mg tid | Sedative | ||
Hydroxyzine (Atarax®) | 25–100 mg tid | Sedative | ||
Levocetrizine (Xyzal®) | 5 mg daily | Mild sedative | ||
Promethazine (Phenergan®) | 25–100 mg tid–qid | Sedative | ||
Herbs | Valerian | 300–900 mg daily HS | ||
Supplements | Melatonin | 3 mg HS | ||
Nondrug | Hypnosis | HS | Avoid use driving | |
Progressive relaxation | HS |
Abbreviations: HS, at bedtime; qid, four times daily; tid, three times daily.
Antipruritics
While no really effective antipruritic drugs have been developed, sedating antihistamines may be helpful (see Table 4). Topical antipruritics may also offer relief (see Table 5).
Table 5.
Category | Agent | Dosage | Side effects | Cautions |
---|---|---|---|---|
Herbs | Capsaicin | Topical qid | Burning sensation | Avoid eyes |
Camphor | Topical prn | |||
Menthol | Topical prn | |||
Nondrug | Hypnosis | Daily and prn | Avoid use driving |
Abbreviations: Prn, per required need; qid, four times daily.
Complementary pharmacological psychocutaneous therapies
Herbs and supplements
Herbal therapy in dermatology was reviewed by Bedi and Shenefelt84 and use of herbs and supplements in dermatology by Levin and Maibach.85 Further information about individual herbs, their actions, interactions, and adverse effects is available in the PDR for Nonprescription Drugs, Dietary Supplements and Herbs,86 The Complete German Commission E Monographs,87 and in many other textbooks and monographs. Psychoactive herbs and supplements that may have some indirect impact on skin diseases through anxiolytic, antidepressant, or soporific activities are of particular interest in psychosomatic dermatology. Herbal therapy in psychiatry was reviewed by Sarris.88 See the current PDR for Nonprescription Drugs, Dietary Supplements and Herbs for details of their actions, interactions, adverse effects, and literature references.
Antidepressants
Saint John’s wort is approved by the German Commission E for depression. It is helpful in mild to moderate depression but not for severe depression.89 It induces cytochrome P450 which changes the metabolism of a number of other drugs. S-adenosyl-L-methionine (SAMe) is also taken as an antidepressant. A meta-analysis of studies comparing SAMe with controls showed significant clinical improvement with SAMe similar to that of standard SSRI treatment, with fewer side effects90 (see Table 1).
Anxiolytics
Aromatherapy with lavender oil has been shown to produce a significant reduction in anxiety. Lemon balm has been approved by the German Commission E for nervousness and insomnia. Kava kava has moderate anxiolytic effects, but its use is not recommended because of its potential hepatotoxicity. Magnolia bark has moderate anxiolytic effects91 and has been used in Japan for a number of years. Passion flower has been approved by the German Commission E for nervousness and insomnia (see Table 3).
Soporifics
Melatonin can produce drowsiness. When it is taken, caution should be used in operating machinery. Valerian has been approved by the German Commission E for insomnia caused by nervousness (see Table 4).
Nonpharmacologic treatments for psychocutaneous disorders
Placebo and nocebo
Expectation forms the basis for the placebo effect. The use of placebo remains controversial.92,93 The patient expectations, the doctor’s expectations, and the doctor-patient relationship can affect the patient’s experience of treatment, reduce pain, and influence outcome. While positive expectations or suggestions can produce positive placebo results, negative expectations or suggestions can produce negative nocebo results.94 Research on the placebo effect illustrates the extent to which the natural healing capacities of individuals can be enhanced and nurtured.95 In some common dermatologic conditions, such as acne and urticaria, the placebo effect is about 30%.96 Those skin disorders higher on the Griesemer scale67 are more likely to have a significant placebo effect.
Suggestion
Suggestion is the effect that words, intonation, and/or nonverbal cues have by association that can be used to change subjective perceptions, reduce pain, and influence outcome. Suggestion has been used to promote healing since antiquity. Bloch97 and Sulzberger and Wolf 98 reported on the efficacy of suggestion in treating verruca vulgaris (warts), and that efficacy has since been confirmed numerous times to a greater or lesser degree,99–102 but failed to be confirmed in a few studies.103,104 A recent study that showed negative results was criticized for using a negative suggestion of not feeding the warts rather than a positive suggestion about having the warts resolve.105
Cognitive-behavioral methods
Cognitive-behavioral methods alter dysfunctional habits by interrupting and altering dysfunctional thought patterns (cognitions) or actions (behaviors)106 that damage the skin or interfere with dermatologic therapy. Skin diseases responsive to cognitive-behavioral methods include acne excoriée, atopic dermatitis, factitious cheilitis, hyperhidrosis, lichen simplex chronicus, needle phobia, neurodermatitis, onychotillomania, prurigo nodularis, trichotillomania, and urticaria. Adding hypnosis to cognitive-behavioral therapy can facilitate aversive therapy and enhance desensitization and other cognitive-behavioral methods.107
Biofeedback
Biofeedback can enhance the patient’s awareness of tension and help them to relax, improving skin disorders that flare with stress or that have an autonomic nervous system aspect. Biofeedback of GSR can help reduce hyperhidrosis (excess sweating). Biofeedback of skin temperature by temperature-sensitive strip or by thermocouple can be used for relaxation,9 dyshidrosis, and Raynaud’s syndrome.108–110 HRV biofeedback can also help reduce the stress response that tends to exacerbate many inflammatory skin disorders. Hypnosis can produce relaxation and enhance the effects produced by biofeedback.107
Hypnosis
Hypnosis has many useful dermatologic applications. Medical hypnotherapy involves guiding the patient into a trance state of narrowed awareness, focused attention, selective wakefulness, and heightened suggestibility for a specific purpose such as relaxation, pain or pruritus reduction, or habit modification. The hypnotic trance compared with the usual waking state has objectively documented differences in regional cerebral blood flow111 and EEG112 patterns. One way that hypnosis may make suggestions more effective is by inhibiting competing thoughts so that the focus can be solely on the suggestion.113 Hypnosis may improve or clear numerous skin disorders. Examples include acne excoriée, alopecia areata, atopic dermatitis, congenital ichthyosiform erythroderma, dyshidrotic dermatitis, erythromelalgia, furuncles, glossodynia, herpes simplex, hyperhidrosis, ichthyosis vulgaris, lichen planus, neurodermatitis, nummular dermatitis, post-herpetic neuralgia, pruritus, psoriasis, rosacea, trichotillomania, urticaria, verruca vulgaris, and vitiligo.7 Generally, high and medium hypnotizables respond better than low hypnotizables, although for many purposes light trance is all that is necessary. Dermatologists should generally not use hypnosis with schizophrenics or others who are not mentally intact. Hypnosis also can reduce anxiety and pain associated with dermatologic procedures. Hypnoanalysis has been successful with reducing erythema nodosum, herpes simplex reactivation, neurodermatitis, neurotic excoriations, rosacea, urticaria, and verrucae (viral warts).25
Conclusion
Skin disorders that produce changes in the appearance of skin, hair, or nails, or changes in sensation can have a major impact on the psyche. Treating the skin disorder effectively often induces psychosocial improvement. The psyche through psychoneuroimmunoendocrine and behavioral mechanisms can in turn have a major impact on skin disorders. Treating the psyche effectively can improve many inflammatory skin disorders. The psychotropic drugs listed above are often somewhat effective by themselves. Adding non-drug psychocutaneous modalities such as biofeedback, cognitive-behavioral methods, hypnosis, or suggestion often synergistically enhance the treatment response. Teaching patients to practice safe stress using these nonpharmacologic methods, supplemented if necessary with anxiolytic standard drugs or herbal alternatives, is important, since many inflammatory skin disorders are worsened by stress. Exercise, meditation, music therapy, progressive relaxation, self-hypnosis, and other stress-reducing methods can enhance overall health and resiliency, as well as achieving improvement in specific skin disorders.
Footnotes
Disclosure
The author reports no conflicts of interest in this work.
References
- 1.Zane LT. Psychoneuroendocrinimmunodermatology: Pathophysiological mechanisms of stress in cutaneous disease. In: Koo JYM, Lee CS, editors. Psychocutaneous Medicine. New York, NY: Marcel Dekker; 2003. pp. 65–95. [Google Scholar]
- 2.Harth W, Gieler U, Kunir D, Tausk FA. Clinical Management in Psychodermatology. Berlin, AG: Springer Verlag; 2009. pp. 195–208. [Google Scholar]
- 3.Fried RG. Nonpharmacologic treatments in psychodermatology. Dermatol Clin. 2002;20:177–185. doi: 10.1016/s0733-8635(03)00055-x. [DOI] [PubMed] [Google Scholar]
- 4.Jaffarany M. Psychodermatology: A guide to understanding common psychocutaneous disorders. Prim Care Companion J Clin Psychiatry. 2007;9:203–213. doi: 10.4088/pcc.v09n0306. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 5.Poot F, Sampogna F, Onnis L. Basic knowledge in psychodermatology. J Eur Acad Dermatol Venereol. 2007;21:227–234. doi: 10.1111/j.1468-3083.2006.01910.x. [DOI] [PubMed] [Google Scholar]
- 6.Griesemer RD. Emotionally triggered disease in a dermatological practice. Psychiatr Ann. 1978;8:49–56. [Google Scholar]
- 7.Shenefelt PD. Hypnosis in dermatology. Arch Dermatol. 2000;136:393–399. doi: 10.1001/archderm.136.3.393. [DOI] [PubMed] [Google Scholar]
- 8.Urpe M, Buggiani G, Lotti T. Stress and psychoneuroimmunologic factors in dermatology. Dermatol Clin. 2005;23:609–617. doi: 10.1016/j.det.2005.05.017. [DOI] [PubMed] [Google Scholar]
- 9.Shenefelt PD. Relaxation, meditation, and hypnosis for skin disorders and procedures. In: deLuca BN, editor. Mind-Body and Relaxation Research Focus. Hauppauge, NY: Nova Science Publishers; 2008. pp. 45–63. [Google Scholar]
- 10.Barrios AA. Towards Greater Freedom and Happiness. 3rd ed. Culver City, CA: Self-Programmed Control Press; 1985. [Google Scholar]
- 11.Zucker TL, Samuelson KW, Muench F, Greenberg MA, Gevirtz RN. The effects of respiratory sinus arrhythmia biofeedback on heart rate variability and posttraumatic stress disorder symptoms: A pilot study. Appl Psychophysiol Biofeedback. 2009;34:135–143. doi: 10.1007/s10484-009-9085-2. [DOI] [PubMed] [Google Scholar]
- 12.Panconesi E. Psychosomatic factors in dermatology: Special perspectives for application in clinical practice. Dermatol Clin. 2005;23:629–633. doi: 10.1016/j.det.2005.05.020. [DOI] [PubMed] [Google Scholar]
- 13.Seyhan M, Aki T, Karincaoglu Y, Ozcan H. Psychiatric morbidity in dermatology patients: Frequency and results of consultations. Indian J Dermatol. 2006;51:18–22. [Google Scholar]
- 14.Lee CS, Koo JYM. The use of psychotropic medications in dermatology. In: Koo JYM, Lee CS, editors. Psychocutaneous Medicine. New York, NY: Marcel Dekker; 2003. pp. 427–451. [Google Scholar]
- 15.Lucky AW. Quantitative documentation of a premenstrual flare of facial acne in adult women. Arch Dermatol. 2004;140:42–44. doi: 10.1001/archderm.140.4.423. [DOI] [PubMed] [Google Scholar]
- 16.Hughes H, Brown BW, Lawlis GF, Fulton JE. Treatment of acne vulgaris by biofeedback relaxation and cognitive imagery. J Psychosom Res. 1983;27:185–191. doi: 10.1016/0022-3999(83)90021-1. [DOI] [PubMed] [Google Scholar]
- 17.Willemson R, Haentjens P, Roseeuw D, Vanderlinden J. Alexithymia in patients with alopecia areata: Educational background much more important than traumatic events. J Eur Acad Dermatol Venereol. 2009;23:1141–1146. doi: 10.1111/j.1468-3083.2009.03255.x. [DOI] [PubMed] [Google Scholar]
- 18.Gupta MA, Gupta AK, Watteel GN. Stress and alopecia areata: A psychodermatologic study. Acta Derm Venereol Stockholm. 1997;77:296–298. doi: 10.2340/0001555577296298. [DOI] [PubMed] [Google Scholar]
- 19.Willemsen R, Vanderlinden J, Deconinck A, Roseeuw D. Hypnotherapeutic management of alopecia areata. J Am Acad Dermatol. 2006;55:233–237. doi: 10.1016/j.jaad.2005.09.025. [DOI] [PubMed] [Google Scholar]
- 20.Pallanti S, Lotti T, Urpe M. Psychoneuroimmunodermatology of atopic dermatitis: From empiric data to the evolutionary hypothesis. Dermatol Clin. 2005;23:695–701. doi: 10.1016/j.det.2005.05.019. [DOI] [PubMed] [Google Scholar]
- 21.Ehlers A, Stangler U, Gieler U. Treatment of atopic dermatitis: A comparison of psychological and dermatological approaches to relapse prevention. J Consult Clin Psychol. 1995;63:624–635. doi: 10.1037//0022-006x.63.4.624. [DOI] [PubMed] [Google Scholar]
- 22.Stewart AC, Thomas SE. Hypnotherapy as a treatment for atopic dermatitis in adults and children. Brit J Dermatol. 1995;132:778–783. doi: 10.1111/j.1365-2133.1995.tb00726.x. [DOI] [PubMed] [Google Scholar]
- 23.Koblenzer CS. Dermatitis artifacta: Clinical features and approaches to treatment. Am J Clin Dermatol. 2000;4:161–163. doi: 10.2165/00128071-200001010-00005. [DOI] [PubMed] [Google Scholar]
- 24.Koldys KW, Meyer RP. Biofeedback training in the therapy of dyshidrosis. Cutis. 1979;24:219–221. [PubMed] [Google Scholar]
- 25.Shenefelt PD. Psychocutaneous hypnoanalysis: Detection and deactivation of emotional and mental root factors in psychosomatic skin disorders. Am J Clin Hypn. 2007;50:131–136. doi: 10.1080/00029157.2007.10401610. [DOI] [PubMed] [Google Scholar]
- 26.Buske-Kirchenbaum A, Geiben A, Wermke C, et al. Preliminary evidence for herpes labialis recurrence following experimentally induced disgust. Psychother Psychosom. 2001;70:86–91. doi: 10.1159/000056231. [DOI] [PubMed] [Google Scholar]
- 27.Scott MJ. Hypnosis in Skin and Allergic Diseases. Springfield, IL: Charles C. Thomas Publishers; 1960. [Google Scholar]
- 28.Lowe NJ, Glaser DA, Eadie N, Daggett S, Kowalski JW, Lai PY. Botulinum toxin type A in the treatment of primary axillary hyperhidrosis: A 52 week multicenter double-blind, randomized, placebo-controlled study of efficacy and safety. J Am Acad Dermatol. 2007;56:604–611. doi: 10.1016/j.jaad.2007.01.009. [DOI] [PubMed] [Google Scholar]
- 29.Hölzle E. Therapie der hyperhidrosis. Hautarzt. 1994;35:7–15. German. [PubMed] [Google Scholar]
- 30.Koray M, Dulger O, Ak G, et al. The evaluation of anxiety and salivary cortisol levels in patients with oral lichen planus. Oral Dis. 2003;9:298–301. doi: 10.1034/j.1601-0825.2003.00960.x. [DOI] [PubMed] [Google Scholar]
- 31.Konuk N, Koca R, Atik L, Muhtar S, Atasoy N, Bostanci B. Psychopathology, depression and dissociative experiences in patients with lichen simplex chronicus. Gen Hosp Psychiatry. 2007;29:232–235. doi: 10.1016/j.genhosppsych.2007.01.006. [DOI] [PubMed] [Google Scholar]
- 32.Ko SM. Underdiagnosed psychiatric syndrome, 2: Pathologic skin picking. Ann Acad Med Singapore. 1999;28:557–559. [PubMed] [Google Scholar]
- 33.Lehman RE. Brief hypnotherapy of neurodermatitis: A case with four-year follow-up. Am J Clin Hypn. 1978;21:48–51. doi: 10.1080/00029157.1978.10403957. [DOI] [PubMed] [Google Scholar]
- 34.Jarvikallio A, Harvima IT, Naukkarinen A. Mast cells, nerves and neuropeptides in atopic dermatitis and nummular eczema. Arch Dermatol Res. 2003;295:1–7. doi: 10.1007/s00403-002-0378-z. [DOI] [PubMed] [Google Scholar]
- 35.Guarneri F, Marini H. An unusual case of perioral dermatitis: Possible pathogenic role of neurogenic inflammation. J Eur Acad Dermatol Venereol. 2007;21:410–412. doi: 10.1111/j.1468-3083.2006.01894.x. [DOI] [PubMed] [Google Scholar]
- 36.Arck P, Paus R. From the brain-skin connection: The neuroendocrine-immune misalliance of stress and itch. Neuroimmunomodulation. 2006;13:347–356. doi: 10.1159/000104863. [DOI] [PubMed] [Google Scholar]
- 37.Griffiths CE, Richards HL. Psychological influence in psoriasis. Clin Exp Dermatol. 2001;26:338–342. doi: 10.1046/j.1365-2230.2001.00834.x. [DOI] [PubMed] [Google Scholar]
- 38.Masmoudi J, Maalej I, Masmoudi A, et al. Alexithymie et psoriasis: Etude cas-temoin a propos de 53 patients. L’Encephalie. 2009;35:10–17. doi: 10.1016/j.encep.2007.11.009. French. [DOI] [PubMed] [Google Scholar]
- 39.Fortune DG, Richards HL, Kirby B, Bowcock, Main CJ, Griffiths CE. A cognitive-behavioural symptom management programme as an adjunct in psoriasis therapy. Br J Dermatol. 2002;146:458–465. doi: 10.1046/j.1365-2133.2002.04622.x. [DOI] [PubMed] [Google Scholar]
- 40.Kabat-Zinn J. Influence of a mindfulness meditation-based stress reduction intervention on rates of skin clearing in patients with moderate to severe psoriasis undergoing phototherapy (UVB) and photochemo-therapy (PUVA) Psychosom Med. 1998;60:625–632. doi: 10.1097/00006842-199809000-00020. [DOI] [PubMed] [Google Scholar]
- 41.Tausk F, Whitmore SE. A pilot study of hypnosis in the treatment of patients with psoriasis. Psychother Psychosom. 1999;68:221–225. doi: 10.1159/000012336. [DOI] [PubMed] [Google Scholar]
- 42.Garnis-Jones S. Psychological aspects of rosacea. J Cutan Med Surg. 1998;((Suppl 4)):9–16. [PubMed] [Google Scholar]
- 43.Sinclair R. Chronic telogen effluvium: A study of 5 patients over 7 years. J Am Acad Dermatol. 2005;52(2 Suppl 1):12–16. doi: 10.1016/j.jaad.2004.05.040. [DOI] [PubMed] [Google Scholar]
- 44.Stein DJ, Gardner JP, Keuthen NJ, Franklin ME, Walkup JT, Woods DW. Trichotillomania, stereotypic movement disorder, and related disorders. Curr Psychiatry Rep. 2007;9:301–302. doi: 10.1007/s11920-007-0036-4. [DOI] [PubMed] [Google Scholar]
- 45.Barabasz M. Trichotillomania: A new treatment. Int J Clin Exp Hypn. 1987;35:146–154. doi: 10.1080/00207148708416050. [DOI] [PubMed] [Google Scholar]
- 46.Shertzer CL, Lookingbill DP. Effects of relaxation therapy and hypnotizability in chronic urticaria. Arch Dermatol. 1987;123:913–916. [PubMed] [Google Scholar]
- 47.Mercan S, Altunay IK, Taskintuna N, Oguteen O, Kayaoglu S. Atypical antipsychotic drugs in the treatment of delusional parasitosis. Int J Psychiatry Med. 2007;37:29–37. doi: 10.2190/M8M5-H1G2-1257-2017. [DOI] [PubMed] [Google Scholar]
- 48.Gupta MA, Gupta AK. Depression and dermatological disorders. In: Koo JYM, Lee CS, editors. Psychocutaneous Medicine. New York, NY: Marcel Dekker; 2003. pp. 233–249. [Google Scholar]
- 49.Gupta MA. Somatization disorders in dermatology. Int Rev Psychiatry. 2006;18:41–47. doi: 10.1080/09540260500466832. [DOI] [PubMed] [Google Scholar]
- 50.Shenefelt PD. Using hypnosis to facilitate resolution of psychogenic excoriations in acne excoriée. Am J Clin Hypn. 2004:239–245. doi: 10.1080/00029157.2004.10403603. [DOI] [PubMed] [Google Scholar]
- 51.Gupta MA, Gupta AK, Haberman HF. Neurotic excoriations: A review and some new perspectives. Compr Psychiatry. 1986;27:381–386. doi: 10.1016/0010-440x(86)90014-3. [DOI] [PubMed] [Google Scholar]
- 52.Rosenbaum MS, Ayllon T. The behavioral treatment of neurodermatitis through habit-reversal. Behav Res Ther. 1981;19:313–318. doi: 10.1016/0005-7967(81)90052-8. [DOI] [PubMed] [Google Scholar]
- 53.Rothbaum BO, Ninan PT. Manual for the cognitive-behavioral treatment of trichotillomania. In: Stein DJ, Christenson GA, Hollander E, editors. Trichotillomania. Washington, DC: American Psychiatric Publishing; 1999. pp. 263–284. [Google Scholar]
- 54.Kearney CA, Silverman WK. Treatment of an adolescent with obsessive– compulsive disorder by alternating response prevention and cognitive therapy: An empirical analysis. J Behav Ther Exp Psychiatry. 1990;21:39–47. doi: 10.1016/0005-7916(90)90047-o. [DOI] [PubMed] [Google Scholar]
- 55.Inglese M, Haley HR, Elewski BE. Onychotillomania: 2 case reports. Cutis. 2004;73:171–174. [PubMed] [Google Scholar]
- 56.Kroenke K, Sharpe M, Sykes R. Revising the classification of somato-form disorders: Key questions and preliminary recommendations. Psychosomatics. 2007;48:277–285. doi: 10.1176/appi.psy.48.4.277. [DOI] [PubMed] [Google Scholar]
- 57.Bowe WP, Leyden JJ, Crerand CE, Sarwer DB, Margolis DJ. Body dysmorphic disorder symptoms among patients with acne vulgaris. J Am Acad Dermatol. 2007;57:222–239. doi: 10.1016/j.jaad.2007.03.030. [DOI] [PubMed] [Google Scholar]
- 58.Harth W, Hermes B, Seikowski K, Gieler U. Nihilodermie in der Psychodermatologie. Hautarzt. 2007;58:427–434. doi: 10.1007/s00105-007-1329-6. German. [DOI] [PubMed] [Google Scholar]
- 59.Willemsen R, Roseeuw D, Vanderlinden J. Alexithymia and dermatology: The state of the art. Int J Dermatol. 2008;47:903–910. doi: 10.1111/j.1365-4632.2008.03726.x. [DOI] [PubMed] [Google Scholar]
- 60.Henningsen P, Zipfel S, Herzog W. Management of functional somatic syndromes. Lancet. 2007;369(9565):1691–1692. doi: 10.1016/S0140-6736(07)60159-7. [DOI] [PubMed] [Google Scholar]
- 61.Harnack D, Scheel M, Mindt A, Kupsch A, Heinz A, Strohle A. Pregabalin in patients with antidepressant treastment-resistant somatiform disorders: A case series. J Clin Psychopharmacol. 2007;27:537–539. doi: 10.1097/JCP.0b013e31814e5e84. [DOI] [PubMed] [Google Scholar]
- 62.Weisshaar E, Kucenic MJ, Fleischer AB. Pruritus: A review. Acta Derm Venereol. 2003;213(Suppl):5–32. [PubMed] [Google Scholar]
- 63.Gupta MA, Gupta AK. Medically unexplained cutaneous sensory symptoms may represent somatoform dissociation: An empirical study. J Psychosom Res. 2006;60:131–136. doi: 10.1016/j.jpsychores.2005.06.061. [DOI] [PubMed] [Google Scholar]
- 64.Walcyk PJ, Elpern DJ. Brachioradial pruritus: A tropical dermopathy. Brit J Dermatol. 1986;115:177–180. doi: 10.1111/j.1365-2133.1986.tb05714.x. [DOI] [PubMed] [Google Scholar]
- 65.Goodkin R, Wingard E, Bernhard JD. Brachioradial pruritus: Cervical spine disease and neurogenic/neurogenic pruritus. J Am Acad Dermatol. 2003;48:521–524. doi: 10.1067/mjd.2003.203. [DOI] [PubMed] [Google Scholar]
- 66.Gick CL, Mirowski GW, Kennedy JS, Bymaster FP. Treatment of glossodynia with olanzapine. J Am Acad Dermatol. 2004;51:463–465. doi: 10.1016/j.jaad.2004.02.016. [DOI] [PubMed] [Google Scholar]
- 67.Eisenberg E, Bameir E, Bergman R. Notalgia paraesthetica associated with nerve root impingement. J Am Acad Dermatol. 1997;37:998–1000. doi: 10.1016/s0190-9622(97)70083-5. [DOI] [PubMed] [Google Scholar]
- 68.Eisenberg E, River Y, Shiftrin A, Krivoy N. Antiepileptic drugs in the treatment of neuropathic pain. Drugs. 2007;67:1265–1289. doi: 10.2165/00003495-200767090-00003. [DOI] [PubMed] [Google Scholar]
- 69.Cohen AD, Vander T, Medvendovsky E, et al. Neuropathic scrotal pruritus: Anogenital pruritus is a symptom of lumbosacral radiculopathy. J Am Acad Dermatol. 2005;52:61–66. doi: 10.1016/j.jaad.2004.04.039. [DOI] [PubMed] [Google Scholar]
- 70.Weichert GE. An approach to the treatment of anogenital pruritus. Dermatol Ther. 2004;17:129–133. doi: 10.1111/j.1396-0296.2004.04013.x. [DOI] [PubMed] [Google Scholar]
- 71.Kessler RC, Berglund P, Demler O, et al. Lifetime prevalence and age-of-onset distributions of DSM-IV disorders in the National Comorbidity Survey Replication. Arch Gen Psychiatry. 2005;62:593–602. doi: 10.1001/archpsyc.62.6.593. [DOI] [PubMed] [Google Scholar]
- 72.Picardi A, Abenia D, Melchi CF, Puddu P, Pasquini P. Psychiatric morbidity in dermatological outpatients: An issue to be recognized. Brit J Dermatol. 2000;143:983–991. doi: 10.1046/j.1365-2133.2000.03831.x. [DOI] [PubMed] [Google Scholar]
- 73.Sampogna F, Picardi A, Chren MM, et al. Association between poorer quality of life and psychiatric morbidity in patients with different dermatological conditions. Psychosom Med. 2004;66:620–624. doi: 10.1097/01.psy.0000132869.96872.b2. [DOI] [PubMed] [Google Scholar]
- 74.Schulpis K, Georgala S, Papakonstantinou ED, et al. The psychological and sympatho-adrenal status in patients with cystic acne. J Eur Acad Dermatol Venereol. 1999;13:24–27. [PubMed] [Google Scholar]
- 75.Hull PR, D’Arcy C. Acne, depression, and suicide. Dermatol Clin. 2005;23:665–674. doi: 10.1016/j.det.2005.05.008. [DOI] [PubMed] [Google Scholar]
- 76.Wysowski DK, Pitts M, Beitz J. An analysis of reports of depression and suicide in patients treated with isotretinoin. J Am Acad Dermatol. 2001;45:515–519. doi: 10.1067/mjd.2001.117730. [DOI] [PubMed] [Google Scholar]
- 77.Gupta MA, Gupta AK, Schork NJ. Depression modulates pruritus perception: A study of pruritus in psoriasis, atopic dermatitis, and chronic idiopathic urticaria. Psychosom Med. 1994;56:36–40. doi: 10.1097/00006842-199401000-00005. [DOI] [PubMed] [Google Scholar]
- 78.Stoddard FJ, Stroud L, Murphy JM. Depression in children after recovery from severe burns. J Burn Care Rehabil. 1992;13:340–347. doi: 10.1097/00004630-199205000-00007. [DOI] [PubMed] [Google Scholar]
- 79.Herbert TB, Cohen S. Depression and immunity: A meta-analytic review. Psychol Bull. 1993;113:472–486. doi: 10.1037/0033-2909.113.3.472. [DOI] [PubMed] [Google Scholar]
- 80.Dogra S, Kanawar AJ. Skin diseases: Psychological and social consequences. Indian J Dermatol. 2002;47:197–201. [Google Scholar]
- 81.Sampogna F, Raskovic D, Guerra L, et al. Identification of categories at risk for high quality of life impairment in patients with vitiligo. Br J Dermatol. 2008;159:351–359. doi: 10.1111/j.1365-2133.2008.08678.x. [DOI] [PubMed] [Google Scholar]
- 82.Papadopoulos L, Bor R, Legg C. Coping with the disfiguring effects of vitiligo: A preliminary investigation into the effects of cognitive-behavioural therapy. Br J Med Psychol. 1999;72:385–396. doi: 10.1348/000711299160077. [DOI] [PubMed] [Google Scholar]
- 83.PDR Staff. 64th ed. Montvale, NJ: 2010. 2010 Physician’s Desk Reference. [Google Scholar]
- 84.Bedi MK, Shenefelt PD. Herbal therapy in dermatology. Arch Dermatol. 2002;138:232–242. doi: 10.1001/archderm.138.2.232. [DOI] [PubMed] [Google Scholar]
- 85.Levin C, Maibach H. Exploration of “alternative” and “natural” drugs in dermatology. Arch Dermatol. 2002;138:207–211. doi: 10.1001/archderm.138.2.207. [DOI] [PubMed] [Google Scholar]
- 86.PDR Staff. 2010 PDR for Nonprescription Drugs, Dietary Supplements and Herbs. 31st ed. Montvale, NJ: 2009. [Google Scholar]
- 87.Blumenthal M, editor. The Complete German Commission E Monographs: Therapeutic Guide to Herbal Medicines. Austin, TX: American Botanical Council; 1998. [Google Scholar]
- 88.Sarris J. Herbal medicines in the treatment of psychiatric disorders: A systematic review. Phytother Res. 2007;21:703–716. doi: 10.1002/ptr.2187. [DOI] [PubMed] [Google Scholar]
- 89.Linde K, Ramirez G, Mulrow C, et al. St. Johns wort for depression: An overview and meta-analysis of randomized clinical trials. BMJ. 1996;313:253–258. doi: 10.1136/bmj.313.7052.253. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 90.Bressa G. S-adenosyl-L-methionine (SAMe) as antidepressant: Meta-analysis of clinical studies. Acta Neurol Scand. 1994;154(Suppl):7–14. doi: 10.1111/j.1600-0404.1994.tb05403.x. [DOI] [PubMed] [Google Scholar]
- 91.Kuribara H, Stavinoha WB, Maruyama Y. Behavioral characteristics of honkiol, an anxiolytic agent present in extracts of magnolia bark, evaluated by an elevated plus-maze test in mice. J Pharm Pharmacol. 1998;50:819–826. doi: 10.1111/j.2042-7158.1998.tb07146.x. [DOI] [PubMed] [Google Scholar]
- 92.Hrobjartsson A, Gotzche PC. Is the placebo powerless? An analysis of clinical trials comparing placebo with no treatment. N Eng J Med. 1994;344:1594–1602. doi: 10.1056/NEJM200105243442106. [DOI] [PubMed] [Google Scholar]
- 93.Spiegel D, Kraemer H, Carlson RW. Is the placebo powerless? (Letter) N Eng J Med. 2001;345:1276–1279. [PubMed] [Google Scholar]
- 94.Speigel D. Placebos in practice (Editorial) BMJ. 2004;329:927–928. doi: 10.1136/bmj.329.7472.927. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 95.Di Blasi Z, Reilly D. Placebos in medicine: Medical paradoxes need disentangling (Letter) BMJ. 2005;330:45. doi: 10.1136/bmj.330.7481.45-a. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 96.Gupta MA, Gupta AK. Psychodermatology: An update. J Am Acad Dermatol. 1996;34:1030–1046. doi: 10.1016/s0190-9622(96)90284-4. [DOI] [PubMed] [Google Scholar]
- 97.Bloch B. Über die heilung der warzen durch suggestion. Klin Wochnschr. 1927;6:2271–2275. German. [Google Scholar]
- 98.Sulzberger MB, Wolf J. The treatment of warts by suggestion. Med Rec. 1934;140:552–556. [Google Scholar]
- 99.Obermayer ME, Greenson RR. Treatment by suggestion of verrucae planae of the face. Psychosom Med. 1949;11:163–164. doi: 10.1097/00006842-194905000-00007. [DOI] [PubMed] [Google Scholar]
- 100.Ullman M. On the psyche and warts: I. Suggestion and warts: A review and comment. Psychosom Med. 1959;2:473–488. [PubMed] [Google Scholar]
- 101.Dudek S. Suggestion and play therapy in the cure of warts in children: A pilot study. J Nerv Ment Dis. 1967;145:37–42. doi: 10.1097/00005053-196707000-00005. [DOI] [PubMed] [Google Scholar]
- 102.Sheehan DV. Influence of psychosocial factors on wart remission. Am J Clin Hypn. 1978;20:160–164. doi: 10.1080/00029157.1978.10403924. [DOI] [PubMed] [Google Scholar]
- 103.Clarke GHV. The charming of warts. J Invest Dermatol. 1965;45:15–21. doi: 10.1038/jid.1965.84. [DOI] [PubMed] [Google Scholar]
- 104.Stankler RL. A critical assessment of the cure of warts by suggestion. Practitioner. 1967;198:690–694. [PubMed] [Google Scholar]
- 105.Felt BT, Hall H, Olness K, et al. Wart regression in children: Comparison of relaxation-imagery to topical treatment and equal time interventions. Am J Clin Hypn. 1998;41:130–138. [Google Scholar]
- 106.Levenson H, Persons JB, Pope KS.Behavior therapy and cognitive therapy Goldman HH.Review of General Psychiatry 5th edNew York, NY: McGraw-Hill; 2000. 472 [Google Scholar]
- 107.Shenefelt PD. Biofeedback, cognitive-behavioral methods, and hypnosis in dermatology: Is it all in your mind? Dermatol Ther. 2003;16:114–122. doi: 10.1046/j.1529-8019.2003.01620.x. [DOI] [PubMed] [Google Scholar]
- 108.Sarti MG. Biofeedback in dermatology. Clin Dermatol. 1998;16:711–714. doi: 10.1016/s0738-081x(98)00052-2. [DOI] [PubMed] [Google Scholar]
- 109.Panconesi E, editor. Lo stress, le emozioni, la pelle. Masson; Milan: 1998. p. 94. [Google Scholar]
- 110.Freedman RR. Quantitative measurements of finger blood flow during behavioral treatments for Raynaud’s disease. Psychophysiol. 1989;26(4):437–441. doi: 10.1111/j.1469-8986.1989.tb01948.x. [DOI] [PubMed] [Google Scholar]
- 111.Rainville P, Hofbauer RK, Bushnell MC, et al. Hypnosis modulates activity in brain structures involved in the regulation of consciousness. J Cognit Neurosci. 2002;14(6):887–901. doi: 10.1162/089892902760191117. [DOI] [PubMed] [Google Scholar]
- 112.Freeman R, Barabasz A, Barabasz M, Warner D. Hypnosis and distraction differ in their effects on cold pressor pain. Am J Clin Hypn. 2000;43:137–148. doi: 10.1080/00029157.2000.10404266. [DOI] [PubMed] [Google Scholar]
- 113.Barrios AA. Understanding Hypnosis: Theory, Scope and Potential. Hauppauge NY: Nova Science Publishers; 2009. pp. 87–90. [Google Scholar]