Psychocutaneous Diseases




Abstract


Psychocutaneous diseases are commonly encountered in the practice of dermatology, and many affected individuals lack insight into their condition or refuse a psychiatric referral. With a systematic approach to evaluation and treatment, such patients can be successfully managed by dermatologists. Psychodermatologic disorders can be conceptualized in two ways: (1) by the type of psychodermatologic condition – primary psychiatric disorder, secondary psychiatric disorder, psychogenic pruritus and dysesthesia, or psychophysiologic disorder; or (2) by the symptom complex and diagnostic pattern of the underlying psychopathology – anxiety, depression, psychosis, and/or obsession–compulsion. Treatment utilizing psychopharmacologic agents and non-pharmacologic therapies can be directed by the underlying psychopathology. This chapter reviews selected primary and secondary psychiatric conditions that are frequently seen by dermatologists.




Keywords

psychocutaneous, psychodermatology, delusions of parasitosis, body dysmorphic disorder, trichotillomania, excoriation (skin-picking) disorder, acne excoriée, dermatitis artefacta, body-focused repetitive behavior, nonsuicidal self-injury, psychopharmacology

 




Introduction


“Psychodermatology” refers to any aspect of dermatology in which psychological factors play a significant role. At least a third of patients seen in dermatology practices require consideration of associated emotional and psychosocial factors for effective management of their skin condition .


Many patients with psychodermatologic problems resist referral to a mental health professional, and some become upset if such a referral is suggested. Ironically, the individuals who are the most psychologically “ill” often have the least insight into the psychogenic nature of their condition and frequently refuse a psychiatric referral. The dermatologist is then faced with two choices. The first is to try to address the psychological condition. If a dermatologist decides to take this route, it is necessary to be familiar with the approach to diagnosis, therapeutic options (both pharmacologic and non-pharmacologic, including potential side effects of medications), and limitations of what can be accomplished in a dermatology practice. The other option is to disregard the psychological problem and allow this component of the patient’s disorder to remain untreated, which is not optimal. Dermatologists can learn to effectively handle psychodermatologic issues within the limits of their training and practice setting. Although less comprehensive than treatment delivered in collaboration with a psychiatrist, in the authors’ opinion, management of these issues by a dermatologist is better than no treatment at all.


Clinically useful methods of conceptualizing and classifying psychodermatologic disorders are presented in Fig. 7.1 . This incorporates updates from the fifth edition of the American Psychiatric Association’s Diagnostic and Statistical Manual of Mental Disorders (DSM-5™) . Selected primary and secondary psychiatric conditions that are commonly encountered in a dermatologic practice are discussed in this chapter. Strategies for the evaluation and management of patients with these disorders are reviewed, including pharmacologic and non-pharmacologic treatments. Disorders characterized by pruritus and dysesthesia are covered in Chapter 6 .




Fig. 7.1


Classification of psychodermatologic disorders.

Psychocutaneous disorders can be conceptualized by: (1) the specific psychodermatologic condition and its classification; and (2) the presenting symptom complex of the underlying psychopathology. Primary psychiatric disorders are those in which the patient has no primary skin disease and all of the cutaneous findings are self-induced. S econdary psychiatric disorders involve the development of psychological problems as the result of a skin disease. Psychophysiologic disorders are those in which a primary skin condition, such as psoriasis, is exacerbated by emotional factors. A particular patient with a psychodermatologic disorder can have a presenting symptom complex with features from one or more of the four major psychopathologic patterns of anxiety, depression, psychosis, and obsessions/compulsions.




Overview


Psychodermatologic disorders can be conceptualized in two ways: (1) by the specific psychodermatologic condition; or (2) by the symptom complex and diagnostic pattern of the underlying psychopathology, including anxiety, depression, psychosis, and obsession–compulsion. The latter approach is useful because knowledge of the psychopathologic manifestations enables the clinician to choose the most appropriate psychopharmacologic agent ( Table 7.1 ). For example, if the underlying psychopathology involves obsessions and/or compulsions, a selective serotonin reuptake inhibitor (SSRI; e.g. fluoxetine) would be a logical choice of therapy .



Table 7.1

Psychopathologic patterns and psychotropic medications used in dermatology.

The pharmacologic treatment of psychodermatologic disorders can be chosen based on the underlying pathophysiology. This list is not exhaustive and focuses on psychotropic medications that are more frequently used in a dermatologic practice. SSRI, selective serotonin reuptake inhibitor.

















































PSYCHOPATHOLOGIC PATTERNS AND PSYCHOTROPIC MEDICATIONS USED IN DERMATOLOGY
Underlying psychopathology and symptom complex Possible pharmacologic treatment Comments and precautions
Anxiety



  • Excessive anxiety and worry



  • Restlessness; feeling “keyed up” or “on edge”



  • Irritability



  • Fatigability



  • Difficulty concentrating or mind going blank



  • Muscle tension or feeling “shaky”



  • Sleep disturbance



  • Somatic symptoms, e.g. dizziness, sweating, palpitations, abdominal complaints

Acute anxiety: Benzodiazepines


  • Clonazepam (0.5–2 mg once or twice daily, as needed)



  • Lorazepam (0.5–2 mg every 6–8 hours, as needed)




  • Treatment not to exceed 4 weeks because of dependency/addiction risk



  • May cause sedation



  • Taper dosage to avoid withdrawal symptoms

Chronic anxiety: Non-benzodiazepines – start low and titrate slowly


  • Azapirone anxiolytic




    • Buspirone (15 mg/day, divided into three doses; increase daily dose by 5 mg every 2-3 days, up to a maximum of 60 mg/day if needed)




  • SSRIs (see Depression below)



  • Tricyclic antidepressants (e.g. doxepin; see Depression below)



  • Serotonin–norepinephrine reuptake inhibitor




    • Venlafaxine, extended release (37.5–75 mg/day, up to 225 mg/day)





  • Onset of action often delayed 2-4 weeks



  • Do not cause dependency/addiction

Depression



  • Depressed mood



  • Anhedonia



  • Unexplained weight loss/gain or appetite change



  • Insomnia or hypersomnia



  • Psychomotor agitation or retardation



  • Fatigue, lack of energy



  • Feelings of hopelessness, worthlessness



  • Excessive guilt



  • Difficulty with concentration, indecisiveness



  • Suicidal ideation/plan



  • Crying spells



  • Preoccupation with physical concerns




  • SSRIs – start at minimal effective dose and increase every week or every other week as tolerated; if no response at 6–8 weeks, then change to a different class of antidepressants




    • Fluoxetine (10–20 mg/day, up to 40 mg/day)



    • Paroxetine (10–20 mg/day, up to 40 mg/day)



    • Sertraline (25–50 mg/day, up to 200 mg/day)



    • Escitalopram (5–10 mg/day, up to 30 mg/day)



    • Citalopram (10–20 mg/day, up to 40 mg/day)





  • SSRIs have a slow onset of action, with full therapeutic response not seen until 6–8 weeks



  • SSRIs may cause gastrointestinal disturbances, sexual dysfunction



  • Avoid abrupt discontinuation of SSRIs, as may cause dysphoria, dizziness, gastrointestinal distress



  • Citalopram and escitalopram can cause dose-dependent QT prolongation




  • Tricyclic antidepressants (TCAs)




    • Doxepin (dosage for pruritus is typically 10–25 mg at bedtime; for depression, typically start at 10–25 mg at bedtime and increase every 1–2 weeks to a therapeutic dose of 25–150 mg at bedtime or up to 300 mg in divided doses, depending on tolerance and disease severity)





  • TCAs can lead to weight gain, cardiac conduction abnormalities, orthostatic hypotension, and anticholinergic side effects



  • Doxepin often causes sedation, especially in the elderly and smaller individuals; should be started at low doses (e.g. 10 mg/day) in these individuals

Psychosis



  • Delusions are the most common feature that presents to dermatologists



  • Fixed false belief that the patient is convinced is true



  • Delusion is usually encapsulated (narrow focus)




  • Pimozide (starting dose is 1 mg/day; increase by 1 mg every 1–2 weeks until optimal response is reached, typically at 4–6 mg/day)




  • Must taper dosage of pimozide and not discontinue abruptly to avoid withdrawal symptoms such as dyskinetic movements



  • Pimozide is associated with QT prolongation, cardiac toxicity, extrapyramidal side effects (e.g. tardive dyskinesia), and drug interactions (avoid if taking macrolides, protease inhibitors, azole antifungals, grapefruit juice)



  • Baseline ECG often recommended when starting pimozide




  • Atypical (second-generation) antipsychotics




    • Risperidone (1–2 mg/day, up to 4 mg/day)



    • Olanzapine (5–10 mg/day, up to 20 mg/day)



    • Aripiprazole (10–15 mg/day)





  • Weight gain, metabolic effects, and other side effects of atypical antipsychotics are listed in Table 7.2



  • Increasingly being used for delusions of parasitosis because of lower risk of tardive dyskinesia and QT prolongation compared to pimozide.

Obsessive–compulsive disorder (OCD)



  • Presence of intrusive obsessions and/or compulsions (see text)



  • Varying degrees of insight




  • SSRIs (start at low dose and increase every week or every other week until reach therapeutic range)




    • Fluoxetine (20 mg/day, up to 40–80 mg/day)



    • Paroxetine (20 mg/day, up to 40–60 mg/day)



    • Sertraline (50 mg/day, up to 200 mg/day)



    • Fluvoxamine (50 mg/day, up to 200–300 mg/day)



    • Escitalopram (10 mg/day, up to 20–40 mg/day)



    • Citalopram (20 mg/day, up to 40 mg/day)





  • OCD often requires higher doses of SSRIs, and patients may take longer to respond (e.g. 10–12 weeks)



  • Once a therapeutic response is achieved, continue treatment for 1–2 years, followed by gradual tapering of the dosage




  • Tricyclic antidepressants




    • Clomipramine (50 mg/day, up to 100–250 mg/day)





  • Clomipramine has a less tolerable side-effect profile than SSRIs, including cardiac toxicity and arrhythmias; check blood levels when the dose is ≥150 mg/day




  • Serotonin–norepinephrine reuptake inhibitor




    • Venlafaxine (75 mg/day, up to 225–350 mg/day)





  • Venlafaxine may cause hypertension and an increased risk of gastrointestinal bleeding



In the classification method based on psychodermatologic conditions, most patients can be grouped into one of four categories (see Fig. 7.1 ):




  • primary psychiatric disorders , in which the patient has no primary skin disease and all of the cutaneous findings are self-induced, as in delusions of parasitosis



  • secondary psychiatric disorders , in which the patient develops psychological problems as a result of a skin disease



  • psychogenic pruritus and dysesthesia , in which the patient presents with a purely sensory complaint (e.g. pruritus, burning, stinging) without evidence of a primary skin disease or underlying medical condition (see Ch. 6 )



  • psychophysiologic disorders , in which a primary skin disorder (e.g. atopic dermatitis) is exacerbated by emotional factors (e.g. anxiety)





Primary Psychiatric Disorders With Dermatologic Manifestations


Delusions of Parasitosis




Synonyms


▪ Delusional parasitosis ▪ Delusional infestation ▪ Ekbom syndrome



Key features





  • Fixed, false belief that the skin is infested with parasites



  • May experience sensations of biting, crawling, or stinging



  • Need to distinguish from substance-induced formication



  • Requires treatment with an antipsychotic medication




Introduction


Delusions of parasitosis is classified as a somatic type of delusional disorder (previously referred to as monosymptomatic hypochondriacal psychosis) within the broad group of schizophrenia spectrum and other psychotic disorders . Delusions are defined as fixed beliefs that are not amenable to change despite conflicting evidence, and somatic delusions are focused on bodily functions or sensations. Individuals with delusions of parasitosis have the isolated, fixed belief that their skin is infested by parasites, in the absence of any objective evidence of infestation .


Clinical features


Patients with delusions of parasitosis do not meet criteria for a diagnosis of schizophrenia. However, they should fulfill the DSM-5™ diagnostic criteria for a delusional disorder which are: (1) the delusion must be present for ≥1 month; (2) the patient does not exhibit impaired functioning or bizarre behavior apart from the impact of the delusion; and (3) the delusion cannot be attributable to the effects of a substance, medication, medical condition, or other psychiatric disorder . The delusional belief is “encapsulated”, i.e. there is a narrow and specific focus on skin infestation. Patients may be able to state that others view their beliefs as irrational (“factual insight”), but they lack the true insight necessary to personally accept the valid explanation.


Individuals with delusions of parasitosis typically present with a history of symptoms for months or even years. They have often already been evaluated by many physicians and have tried to eradicate their alleged “parasites” by methods such as using pesticides, hiring exterminators, or changing their residence. Patients frequently bring in bits of skin, lint, and other samples that they believe represent “parasites”, which is referred to as the “matchbox sign” ( Fig. 7.2 ). They may report cutaneous sensations of crawling, biting, or stinging.




Fig. 7.2


Delusions of parasitosis.

A Multiple excoriations and hypopigmented scars resulting from the patient’s attempts to “dig out” parasites. B Samples of alleged “parasites” brought in by a patient (“matchbox sign” or “specimen sign”).

Courtesy, Kalman Watsky, MD.


Skin findings in delusions of parasitosis range from none to excoriations, lichenification, prurigo nodularis, and ulcerations (see Fig. 7.2 ). All of these are self-induced, usually resulting from the patient’s efforts to dig out “parasites”.


One intriguing aspect of this disorder is the potential for a shared delusional system whereby the patient’s close contacts come to believe in the delusion as well. Folie à deux (“craziness for two”) is the term used to describe two people who share the same delusion. Occasionally, larger numbers of people harbor the same delusion, which may include the patient’s parent(s) and children .


Morgellons disease is a controversial condition with manifestations that fall within the spectrum of delusions of parasitosis . A hallmark of this disorder is that patients claim to observe fibers exuding from their skin, and it has received widespread media and Internet coverage. Multiple articles in the medical literature and investigation by the Centers for Disease Control and Prevention support the categorization of Morgellons disease as a form of delusions of parasitosis .


Epidemiology


The average age of onset is 55–60 years . Among individuals over 50 years of age, women experience the disorder twice as often as men; however, prior to age 50, men and women are equally affected. Younger patients with this disorder are usually of a lower socio-economic status and may have a history of substance abuse, while older patients are frequently of a higher socio-economic status.


Differential diagnosis


Delusions of parasitosis is distinct from formication , which represents a tactile hallucination involving the sensation of “bugs” crawling within or biting the skin. Formication does not involve a fixed, false belief that the sensations are caused by a skin infestation. Formication and/or delusions of skin infestation can result from use of drugs, especially amphetamines and cocaine (see Ch. 89 ). As noted above, patients with delusions due to the effects of a substance, medication, medical condition (e.g. true skin infestation, neurologic disorder), or other psychiatric disorder (e.g. schizophrenia, depression with psychotic features) are excluded from diagnosis of delusions of parasitosis.


Management


One of the most challenging aspects of management is getting patients with delusions of parasitosis to agree to take an antipsychotic medication. The first step is to establish rapport and address their concerns seriously without challenging their beliefs, making sure to do a thorough dermatologic examination. When discussing the diagnosis with the patient, communicate it in a matter-of-fact manner and refrain from making any statements that may be misinterpreted by the patient as supporting his/her delusional ideation. Often, it is more feasible to present the antipsychotic medication as one that may work empirically for symptoms of formication and agitation rather than to confront the individual about psychiatric issues. If the medication is presented in an objective and pragmatic manner, the patient may have less difficulty accepting it as a therapy.


The treatment of choice for delusions of parasitosis has traditionally been pimozide ( Tables 7.1 and 7.2 ). As part of the discussion on therapy, the dermatologist should explain to the patient that he or she does not have Tourette syndrome (the FDA-approved indication for pimozide) or schizophrenia. There have been multiple reports of successful treatment of delusions of parasitosis with atypical antipsychotic medications (e.g. risperidone, olanzapine, aripiprazole), which have more favorable side-effect profiles (see Tables 7.1 and 7.2 ). Patients with delusions of parasitosis can often be successfully tapered off medication after 2–6 months of therapy.


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Sep 15, 2019 | Posted by in Dermatology | Comments Off on Psychocutaneous Diseases

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