- Clinical science
Alopecia is the loss of hair from any hair-bearing area of the body, but most often the scalp. It may be congenital or acquired, circumscribed or diffuse, and cicatricial or nonscarring. Androgenetic alopecia, a type of diffuse, nonscarring, acquired alopecia, is the most common, affecting > 70% of the general population by 70 years of age. Alopecia areata, an acquired, circumscribed, nonscarring alopecia, is the next most common type. Clinical diagnosis is usually possible. In ambiguous cases, diagnosis is aided by microscopic examination of the hair, trichograms, and scalp biopsy. Treatment depends on the type of alopecia and includes long-term (at least 1 year) use of topical minoxidil, corticosteroids (topical, intralesional, or oral), or antiandrogens. Surgery (hair transplant) or camouflaging techniques are used when medical therapy fails. The prognosis is variable and depends on the etiology and severity of hair loss.
- Alopecia: : loss of hair (baldness)
- Effluvium : process of hair loss
- Atrichia : inherited hair loss
- Hypotrichosis : congenital sparse hair, which is usually associated with syndromes such as Netherton syndrome and Rothmund-Thomson syndrome
- Anagen phase: phase of active growth
- Telogen phase: resting phase
- Catagen phase: phase of follicular regression
|According to etiology (congenital/acquired) and pattern (diffuse/circumscribed)||According to scarring or nonscarring types|
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- The diagnosis is often clear from the patient history and physical examination.
- Hair pull test: About 50 strands of hair are lightly tugged away from the scalp; if > 5 strands can be pulled out, the test is positive.
- Dermoscopy: examination of the scalp skin, follicle size and hair shaft diameter by magnification
- Microscopic examination of hair follicles and shaft: to determine the phase of hair growth (anagen, telogen) and structural abnormalities of the shaft
- Scalp biopsies from sites of active disease: to confirm diagnosis of cicatricial alopecia
- Trichograms: aids diagnosis and prognosis of nonscarring alopecia
Congenital diffuse alopecia
- Trichorrhexis nodosa: A hair shaft deformity characterized by the development of weak points in the shaft due to physical/chemical trauma in genetically predisposed individuals.
- Pili torti: The hair shaft is flattened and has multiple twists → fragile hair which breaks easily
- Monilethrix (beaded hair): Autosomal dominant disorder with beaded hair shafts which break easily, close to the scalp, a few months after birth.
- Genetic syndromes: Menkes disease, Netherton's syndrome, etc.
Acquired diffuse alopecia
- Definition: Androgenetic alopecia is a progressive, nonscarring alopecia; that affects the regions of the scalp with the most androgen-sensitive hair follicles; , resulting in a characteristic pattern of balding (bitemporal scalp in men and vertex and frontal scalp in women).
- Differential diagnosis
|Androgenetic alopecia in men (male pattern baldness)||Androgenetic alopecia in women (female pattern baldness)|
|Clinical features|| |
|Diagnosis|| || |
- The telogen (resting) phase of hair growth predominates → premature shedding of the resting hair follicles → diffuse, nonscarring hair loss
- Endocrine: hypothyroidism, hypopituitarism, hypoparathyroidism, diabetes mellitus.
- Drugs: anabolic steroids, antithyroid drugs, heparin, coumarin, antimetabolites (chemotherapy), oral contraceptives, etc.
- Nutritional: hypervitaminosis A, zinc deficiency, malnutrition states
- Stress: major surgery, sepsis, after childbirth (telogen gravidarum), acute or chronic illness (e.g., ), severe psychological stress
- Hair density reduces by < 50%
- Does not progress to complete baldness.
- Treatment: reassurance and manage underlying condition
Congenital circumscribed alopecia
- Temporal triangular alopecia
- A well demarcated hamartomatous lesion predominantly composed of sebaceous glands
- A solitary hairless, velvety, orange/tan plaque
- Seen in infancy/early childhood
- Risk of malignant degeneration (basal cell carcinoma, squamous cell carcinoma, etc.), esp. at puberty
- Treatment: Surgical excision before puberty
Aplasia cutis congenita
- Intra-uterine developmental disruption of one/more layers of the scalp
- A part of the scalp is missing at birth, which, on healing → scarred, hairless patch
- Treatment: Small lesions: no treatment; Large lesions: surgical excision + primary closure/repair (with help of tissue expanders and skin flaps)
Acquired circumscribed alopecia
- Definition: Hair loss in well demarcated patches due to immune mediated inflammation of hair follicles
- Prevalence: 1 in 1000 people
- Age: mostly in people < 30 years
- Sex: ♂ = ♀
- Abrupt onset (within weeks)
- Smooth, circular, well defined patches of hair loss without scarring (Bland scalp)
- Exclamation point hairs
- Various patterns of distribution
- Ophiasis: Hair loss localized to the back and sides of the scalp
- Sisiapho: Sparing of the sides and back of the scalp
- Extensive alopecia areata: Hair loss affecting > 50% of the scalp
- Alopecia universalis : All hair bearing sites are affected Alopecia universalis mimics telogen effluvium
- Alopecia totalis: Complete baldness
- Nail involvement (up to 40% of cases): nail pitting, onycholysis, Beau lines, etc.
- Other autoimmune disorders may be present (e.g., vitiligo, autoimmune disorders of the thryoid, etc.)
- Diagnostics: usually clinical, biopsy rarely necessary + histology, trichogram
- Trichotillomania: Compulsive pulling out of one's own hair → ill defined patchy hair loss and hairs of different lengths.
- Loose anagen syndrome: Abnormal keratinization of the hair root → poor anchoring of the hair follicle to the scalp → hair falling out in clumps with minimal traction
- : The affected areas of scalp are scaly compared to the smooth hair loss of alopecia
- Secondary syphilis: patchy hair loss → moth-eaten appearance of scalp
- Brocq pseudopelade
- Prognosis: Is poor for alopecia universalis and totalis