Updated: Sep 23, 2009
Trichotillomania is characterized by the persistent and excessive pulling of one's own hair, resulting in noticeable hair loss. In 1889, Hallopeau, a Greek dermatologist, first used the word trichotillomania to describe a patient who pulled out his hair.1 Despite this first description of trichotillomania in the late 1800s, little is understood about the disorder in children.
Hair pulling in trichotillomania can occur on any part of the body where hair grows. The most common area of hair pulling is the scalp, followed by the eyelashes and eyebrows.2 However, hair pulling also can occur in the pubic region and any other area of the body with hair. The alopecia that results from hair pulling can range from small undetectable areas of hair loss to total baldness.
The Diagnostic and Statistical Manual of Mental Disorders, Fourth Edition (DSM-IV-TR) classifies trichotillomania as an impulse-control disorder.3 The hair-pulling behavior can occur during both relaxed and stressful times, but people with trichotillomania often experience a mounting sense of tension before hair pulling occurs or when attempting to resist the behavior. In addition, as noted in the DSM-IV-TR, a "gratification" or "sense of relief" occurs after the hair is pulled. Therefore, at times, trichotillomania may be described better as a type of obsessive-compulsive disorder (OCD) because of its compulsivelike nature.
In many individuals, adolescent-onset trichotillomania indicates more severe psychopathology as an impulse-control disorder or OCD, whereas preschool-onset trichotillomania is often described as a childhood habit disorder. Trichotillomania in younger children is often mistaken for a short-term habit of hair pulling; therefore, careful analysis of the duration of the behavior is important for making the diagnosis because the behavior must last several months to be considered trichotillomania.
Trichotillomania can cause a child to experience distress and may result in moderate impairment in social or academic functioning.2 Additionally, trichotillomania may result in impairment in other important areas of functioning, such as family relationships.
The DSM-IV-TR diagnostic criteria for trichotillomania include (1) recurrent pulling out of one's hair, resulting in noticeable hair loss, (2) an increasing sense of tension immediately before pulling out the hair or when attempting to resist the behavior, (3) pleasure, gratification, or relief when pulling out the hair, (4) the disturbance is not better accounted for by another mental disorder and is not due to a general medical condition (eg, a dermatologic condition), and (5) the disturbance causes clinically significant distress or impairment in social, occupational, or other important areas of functioning.3
Trichotillomania results in highly variable patterns of hair loss. The scalp is the most common area of hair pulling, followed by the eyebrows, eyelashes, pubic and perirectal areas, axilla, limbs, torso, and face. The resulting alopecia can range from thin unnoticeable areas of hair loss to total baldness in the area(s) being plucked. In addition, trichophagia (ie, mouthing and/or ingesting hair) is common in persons who pull out their hair. This chewing or mouthing behavior can frequently lead to the formation of trichobezoars (ie, hair casts) in the stomach or small intestines. Trichobezoars can result in anemia, abdominal pain, hematemesis, nausea and/or vomiting, bowel obstruction, perforation, gastrointestinal (GI) bleeding, acute pancreatitis, and obstructive jaundice.
Accurate prevalence rates of trichotillomania are difficult to approximate due to the frequent denial of the disorder and the failure of many individuals with the disorder to seek professional intervention. Therefore, as indicated in the DSM-IV-TR, exact systematic data on prevalence rates of trichotillomania are limited.
Although US epidemiologic studies on the prevalence rate of trichotillomania are rare, estimates indicate that approximately 8 million people have trichotillomania. An accurate prevalence rate is difficult to achieve because of individuals who attempt to hide the disorder. Future studies are needed to confirm the prevalence rates. In a study of college students, approximately 1%-2% had past or current symptoms of trichotillomania.4 Although empiric data are not available, some studies indicate that substantially more children suffer from trichotillomania than adults.
Trichotillomania results in highly variable patterns of hair loss, ranging from small undetectable patches of hair loss to total baldness. Ingestion of the pulled hair can result in trichobezoar formation and subsequent anemia, abdominal pain, hematemesis, nausea and/or vomiting, bowel obstruction, perforation, GI bleeding, pancreatitis, and obstructive jaundice.
No prevalence rates of trichotillomania among various racial groups are available.
In children, trichotillomania is typically observed in equal numbers of males and females. Among adults, more females than males present with the disorder. Exact estimates of sex differences are limited.
Trichotillomania is frequently a chronic disorder (lasting weeks to decades), with a variable age of onset. According to the DSM-IV-TR, the following age data exist:
Trichotillomania can be difficult to diagnose. Symptoms may include pulling hair (resulting in alopecia), denying hair-pulling behavior, pulling hairs from other objects or people, avoiding social situations, experiencing increased stress and anxiety levels, and experiencing GI complaints related to trichobezoar formation.
Physical signs of trichotillomania may include variable patterns of alopecia or hair thinning, hair abnormalities, and trichobezoar formation.
The etiology of trichotillomania continues to be unknown. However, the following explanations are proposed hypotheses for the onset and maintenance of the hair-pulling behavior:
Anxiety Disorder: Obsessive-Compulsive
Disorder
Tinea capitis
Alopecia areata (Approximately 33% of children who have trichotillomania are misdiagnosed as having alopecia areata. Therefore, a confirmed thorough assessment is important.)
Traction alopecia
Male pattern baldness
Other causes of alopecia (eg, infections, medications, febrile illnesses, crash diets)
Other mental disorders
Systematic diseases (eg, cancer, leukemia, Hodgkin disease, cirrhosis, hypothyroidism, tuberculosis)
Anxiety Disorder: Habit
Stereotypic movement disorder
Factitious disorder with predominately physical signs and symptoms
Short-term habit in children
See Procedures.
After a diagnosis of trichotillomania is confirmed through a workup, take the following actions:
Consider removal of trichobezoars in the stomach and intestines.
Consult with psychiatry, psychology, or developmental-behavioral pediatrics specialists.
A child with trichotillomania requires no special diet.
No activity limitations are suggested for a child with trichotillomania. However, if the hair-pulling behavior is associated with a specific activity, that specific activity may require close monitoring. As indicated in a study of individuals with trichotillomania, the following are possible activities during which patients with trichotillomania may engage in hair pulling:
Few drug studies on trichotillomania in children and adults exist. However, SSRIs have demonstrated a degree of effectiveness in some patients with trichotillomania. In children, SSRIs (eg, fluoxetine, sertraline, fluvoxamine) may be more advantageous as a medication choice than tricyclic antidepressants (TCAs) because of their milder adverse effects.
Physicians are advised to be aware of the following information and use appropriate caution when considering treatment with antidepressants in the pediatric population.
In December 2003, the UK Medicines and Healthcare Products Regulatory Agency (MHRA) issued an advisory that most SSRIs are not suitable for use by persons younger than 18 years for treatment of "depressive illness." After review, this agency decided that the risks to pediatric patients outweigh the benefits of treatment with SSRIs, except fluoxetine (Prozac), which appears to have a positive risk-benefit ratio in the treatment of depressive illness in patients younger than 18 years.
In October 2003, the US Food and Drug Administration (FDA) issued a public health advisory regarding reports of suicidality in pediatric patients treated with antidepressant medications. This advisory reported suicidality (both ideation and attempts) in clinical trials of various antidepressant drugs in pediatric patients. The FDA has asked that additional studies be performed, because suicidality occurred in both treated and untreated patients with major depression and thus could not be definitively linked to drug treatment.
However, a recent study of more than 65,000 children and adults treated for depression between 1992 and 2002 by the Group Health Cooperative in Seattle found that suicide risk declines, not rises, with the use of antidepressants. This is the largest study to date to address this issue.8
Currently, evidence does not exist to associate OCD and other anxiety disorders treated with SSRIs with an increased risk of suicide.
Antidepressant agents chemically unrelated to tricyclic, tetracyclic, or other available antidepressants. Inhibits CNS neuronal uptake of serotonin (5-HT). May also have weak effect on norepinephrine and dopamine neuronal reuptake.
SSRIs are greatly preferred over the other classes of antidepressants. Because the adverse effect profile of SSRIs is less prominent, improved compliance is promoted. SSRIs do not have the cardiac arrhythmia risk associated with tricyclic antidepressants. Arrhythmia risk is especially pertinent in overdose, and suicide risk must always be considered when treating a child or adolescent with mood disorder.
Selectively inhibits presynaptic serotonin reuptake with minimal or no effect in reuptake of norepinephrine or dopamine. Approved in children aged 8-18 y for major depressive disorder and in children aged 7-17 y for obsessive compulsive disorder.
20-80 mg/d PO
<7 years: Not established
≥7 years: Initial doses of 10-20 mg/d have been used
Adolescents: Administer as in adults
Increases toxicity of diazepam and trazodone by decreasing clearance; also increases toxicity of MAOIs and highly protein-bound drugs
Documented hypersensitivity; MAOIs concurrently or within previous 14 d
C - Fetal risk revealed in studies in animals but not established or not studied in humans; may use if benefits outweigh risk to fetus
Caution in hepatic impairment and history of seizures; discontinue MAOIs at least 14 d before initiating therapy; recently, the FDA has urged that all antidepressants should be used with caution in children and adolescents, as their use has been associated with increased suicidal ideation
Selectively inhibits presynaptic serotonin reuptake. Approved for children aged 6-17 y with OCD.
50-200 mg/d PO
<6 years: Not established
6-12 years: 25 mg/d PO initially; may gradually increase dose if needed, not to exceed 100 mg/d
13-17 years: 50 mg PO qd; may gradually increase dose if needed; not to exceed 200 mg/d
Increases toxicity of MAOIs, diazepam, tolbutamide, and warfarin
Documented hypersensitivity; MAOIs concurrently or within previous 14 d
C - Fetal risk revealed in studies in animals but not established or not studied in humans; may use if benefits outweigh risk to fetus
Caution in preexisting seizure disorders, recent myocardial infarction, unstable heart disease, and hepatic or renal impairment; recently, the FDA has urged that all antidepressants should be used with caution in children and adolescents, as their use has been associated with increased suicidal ideation
Potent selective inhibitor of neuronal serotonin reuptake. Does not significantly bind to alpha-adrenergic, histamine, or cholinergic receptors and, thus, has fewer adverse effects than TCAs. Approved for OCD in children aged 8 y or older.
50-300 mg/d PO
<8 years: Not established
≥8 years: 25 mg PO qhs initially; in controlled clinical trials, typical dosage range was 50-200 mg/d, not to exceed 200 mg/d for children ≤11 y and 300 mg/d for adolescents
Risk of hypertensive crisis increases with coadministration with MAOIs; fluvoxamine potentiates effect of triazolam and alprazolam and, thus, when taking concurrently, reduce dose by at least 50%; reduce dose of theophylline by one third, and monitor plasma levels if taking concurrently; alcohol, cimetidine, sertraline, phenothiazines, and warfarin increase toxicity
Documented hypersensitivity; MAOIs concurrently or within previous 14 d
C - Fetal risk revealed in studies in animals but not established or not studied in humans; may use if benefits outweigh risk to fetus
Caution in liver dysfunction, cardiovascular disease, and history of seizures or suicidal tendencies; recently, the FDA has urged that all antidepressants should be used with caution in children and adolescents, as their use has been associated with increased suicidal ideation
These antidepressants are structurally related to phenothiazine antipsychotic agents. They exhibit 3 major pharmacologic actions in varying degrees (ie, amine pump inhibition, sedation, anticholinergic action [peripheral and central]). They also inhibit reuptake of norepinephrine or serotonin (ie, 5-hydroxytryptamine, 5-HT) at the presynaptic neuron.
Inhibits reuptake of norepinephrine or serotonin (5-HT) at presynaptic neuron. Approved for children aged 10-17 y for OCD.
<10 years: Not established
10-17 years: 25 mg/d PO qd or in divided doses with meals for 2 wk initially; may increase if needed, not to exceed 3 mg/kg or 100 mg/d, whichever is the smaller dose
25-100 mg/d PO; approved for OCD in children >10 y
May increase effects of CNS stimulants, CNS depressants, MAOIs, sympathomimetics, alcohol, antipsychotics, benzodiazepines, barbiturates, anticholinergic agents, and thyroid medications (cardiac effects); TCAs may decrease effects of clonidine and guanethidine; effects of TCAs may be increased by phenothiazines, methylphenidate, oral contraceptives (estrogen), and marijuana; effects of TCAs may be decreased by lithium, barbiturates, chloral hydrate, and smoking
Documented hypersensitivity; narrow-angle glaucoma; in acute recovery phase following myocardial infarction; current use of MAOI or fluoxetine or use within previous 14 d
C - Fetal risk revealed in studies in animals but not established or not studied in humans; may use if benefits outweigh risk to fetus
May impair mental or physical abilities required for performance of potentially hazardous tasks; caution in cardiovascular disease, conduction disturbances, seizure disorders, urinary retention, hyperthyroidism, and in those receiving thyroid replacement therapy; recently, the FDA has urged that all antidepressants should be used with caution in children and adolescents, as their use has been associated with increased suicidal ideation
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Franklin ME, Flessner CA, Woods DW, Keuthen NJ, Piacentini JC, Moore P, et al. The child and adolescent trichotillomania impact project: descriptive psychopathology, comorbidity, functional impairment, and treatment utilization. J Dev Behav Pediatr. Dec 2008;29(6):493-500. [Medline].
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trichotillomania, childhood habit disorder, impulse-control disorder, hair pulling, obsessive-compulsive disorder, OCD, trichophagia, trichobezoars
Cynthia R Ellis, MD, Director of Developmental Medicine, Associate Professor, Department of Pediatrics and Psychiatry, Munroe Meyer Institute for Genetics and Rehabilitation, University of Nebraska Medical Center
Cynthia R Ellis, MD is a member of the following medical societies: Nebraska Medical Association
Disclosure: Nothing to disclose.
Holly Jean Roberts, PhD, Assistant Professor, Pediatrics, Munroe-Meyer Institute, University of Nebraska Medical Center
Holly Jean Roberts, PhD is a member of the following medical societies: Autism Society of America, National Association of School Psychologists, and Psi Chi
Disclosure: Nothing to disclose.
Connie J Schnoes, MA, PhD, Psychologist, Director of Training, Supervising Practitioner, Father Flanagan's Boys' Home, Boys Town
Disclosure: Nothing to disclose.
Chet Johnson, MD, Medical Director, Child Development Unit, Department of Pediatrics, Professor, University of Kansas Medical Center
Chet Johnson, MD is a member of the following medical societies: American Academy of Pediatrics
Disclosure: Nothing to disclose.
Mary L Windle, PharmD, Adjunct Assistant Professor, University of Nebraska Medical Center College of Pharmacy, Pharmacy Editor, eMedicine
Disclosure: Pfizer Inc Stock Investment from financial planner; Avanir Pharma Stock Investment from financial planner ; WebMD Salary and stock Employment and investment from financial planner
Carrie Sylvester, MD, MPH, Director of Education in Child and Adolescent Psychiatry, Professor, Departments of Psychiatry and Pediatrics, Northwestern University Medical School
Carrie Sylvester, MD, MPH is a member of the following medical societies: American Academy of Child and Adolescent Psychiatry, American Academy of Pediatrics, American Medical Women's Association, American Psychiatric Association, and American Society for Adolescent Psychiatry
Disclosure: Nothing to disclose.
Caroly Pataki, MD, Professor of Clinical Psychiatry and Behavioral Sciences, Department of Psychiatry, Division Chair, Child and Adolescent Psychiatry, Director of Training, Child and Adolescent Psychiatry Residency Program, University of Southern California Keck School of Medicine
Caroly Pataki, MD is a member of the following medical societies: American Academy of Child and Adolescent Psychiatry, New York Academy of Sciences, and Physicians for Social Responsibility
Disclosure: Nothing to disclose.
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