4.2.3 Hirsutism

Grading & Level of Importance: B
Review:
2026

W. Burgdorf, Munich; S. Chee, A. Salam, J. McGrath, London;
Revised by V. del Marmol, Brussels; J. White, Brussels

ICD-11

ED72

Synonyms

Hirsutes, excessive hair, endocrine hypertrichosis.

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Hirsutes, excessive hair, endocrine hypertrichosis; endocrine and para-endocrine hypertrichosis (whereas hirsutism defines an excessive form of hypertrichosis probably due to underlying disease).

Definition

Excessive terminal hair in a male pattern in a woman.

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Excessive, disease-associated, terminal hair in women with a male pattern distribution or ethnic hypertrichosis pattern without endocrinological changes.

Epidemiology

Around 4-11% of women may show signs of hirsutism in several populations. The main manifestation of hyperandrogenism in women is with polycystic ovary syndrome (PCOS), with a prevalence estimated at 65-75%. Certain populations (e.g. far East) may present ethnic hypertrichotic hair patterns not considered as hirsutism. It is a common medical finding affecting approximately 5-15 % of premenopausal women worldwide.

Aetiology & Pathogenesis

Around 5-10% of women may show signs of hirsutism.
There are many different causes.


Endocrine hirsutism: polycystic ovary syndrome; androgen-producing ovarian tumours; congenital adrenal hyperplasia (adrenogenital syndrome); acanthosis nigricans in insulin resistance, adrenal tumours; ACTH-cell hyperplasia; pituitary adenomas (Cushing’s disease); hyperprolactinemia; acromegaly.


Other causes: postmenopausal hirsutism; idiopathic hirsutism; ethnic; medication-induced hirsutism (e.g. anabolic steroids), paraneoplastic.

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There are many different causes and an early and late onset of hirsutism.

Genetically determined in both genders with early onset in a hirsute pattern. This is not ethnic or genetic hypertrichosis. While 80-90 % of women with hirsutism have measurable hyperandrogenemia, the severity of hirsutism and the level of androgen metabolism and excess are not well-correlated. Most probably a peripheral metabolic disorder affects the distribution of hair and within the follicle.

Endocrine hirsutism with late onset around puberty or even later: about 50% of women with hirsutism have endocrine abnormalities: polycystic ovary syndrome; androgen-producing ovarian tumours; congenital adrenal hyperplasia (adrenogenital syndrome); adrenal tumours; ACTH-cell hyperplasia; pituitary adenomas (Cushing’s disease); hyperprolactinemia; acromegaly.

Other causes: postmenopausal hirsutism; idiopathic hirsutism; medication-induced hirsutism (e.g. anabolic steroids).

Signs & Symptoms

Growth of terminal and vellus hairs in woman on upper lip, chin, temples, between breasts, around nipples, on shoulders, linea alba and interior aspects of thighs. Can vary from discrete excess hairs to obvious male pattern with involvement of different locations that are highly variable.

Localisation

Upper lip, chin, temples, breast, abdomen, pubic area, arms, legs, back, buttocks.

Classification

Modified Ferriman-Gallwey system with 19 locations, min 0 to 36 max points. A score of more than 8 indicates androgen excess hirsutism.

Laboratory & other workups

Hormone status (FSH/LH ratio, DHEAS, free testosterone, SHBG,17-hydroxyprogesterone, prolactin), transvaginal ultrasound evaluation of ovaries.

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In most women with hirsutism, the hormone status (FSH/LH ratio, DHEAS, androstendione, free testosterone, 17-hydroxyprogesterone, SHBG, anti-Müllerian hormone, prolactin, TSH) should be assessed and investigations such as a transvaginal ultrasound evaluation of ovaries considered.

Dermatopathology

Usually not required.

Course

Persistent, if an underlying cause cannot be found or treated adequately.

Complications

Psychosocial problems, tendency towards folliculitis after shaving, diabetes and cancer in polycystic ovarian syndrome.

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Psychosocial problems are common. Females suffer very strongly and spend a lot of time and money for hair removal. There is also a tendency towards folliculitis due to shaving and dewaxing. Type 2 diabetes mellitus may be more common if polycystic ovarian syndrome is present.

Diagnosis

Typical hair pattern, endocrine screening with more detailed evaluation if hyperandrogenism is present.

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The diagnosis is usually clinical, with typical hair pattern. Endocrine screening is usually performed with more detailed evaluation if hyperandrogenism is present. Duplex sonography should be considered to exclude superficial thrombophlebitis.

Differential Diagnosis

Ethnic variability. Hypertrichosis. Virilisation. Genetic syndromes causing hypertrichosis (consider especially in children).

Prevention & Therapy

Treat causes of hyperandrogenism.


Mechanical removal of hairs includes shaving, waxing, epilation, electroepilation, laser or light-assisted hair removal. Chemical agents to slow/stop hair growth (e.g. eflornithine). Consider spironolactone, finasteride, cyproterone or oral contraceptives.

 

Psychosocial support.

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Examine and treat the causes of hyperandrogenism and metabolic changes if present.

Mechanical removal of hair includes shaving, waxing, epilation, electroepilation, laser or light-assisted hair removal. Hair growth may be slowed or stopped by chemical means (e.g. eflornithine topically). Consider spironolactone, finasteride, low dose cyproterone acetate or oral contraceptives. Clinical effects may be seen after six to twelve months. Psychosocial support should be offered.

Special

None.

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