Workup and Management of Adult Hair Loss
For adult hair loss, the recommended approach begins with clinical pattern recognition to distinguish alopecia areata (patchy loss with exclamation-mark hairs) from androgenetic alopecia (diffuse central thinning with preserved frontal hairline) or telogen effluvium (diffuse shedding), as laboratory testing is unnecessary when the diagnosis is clinically evident. 1, 2
Initial Clinical Assessment
Pattern recognition is the cornerstone of diagnosis:
- Patchy hair loss with exclamation-mark hairs (short broken hairs at patch margins) confirms alopecia areata and can be identified with dermoscopy 1, 2
- Diffuse central scalp thinning with preserved frontal hairline indicates androgenetic alopecia 2, 3
- Diffuse shedding across the entire scalp suggests telogen effluvium, often precipitated by stress, nutritional deficiency, or recent illness 2, 4
- Scalp inflammation or scaling raises concern for tinea capitis or scarring alopecia and warrants fungal culture or biopsy 2, 5
Key history elements include:
- Duration of hair loss: onset <1 year predicts better prognosis with 34-50% spontaneous remission in limited alopecia areata 1, 2
- Family history: present in 20% of alopecia areata cases 2
- Medication history: chemotherapy causes anagen effluvium 2
- Hair-care practices: tight hairstyles suggest traction alopecia 2
Laboratory Testing Strategy
The British Association of Dermatologists emphasizes that investigations are unnecessary in most cases when the diagnosis is clinically evident. 1, 2
Targeted testing only when diagnosis is uncertain or systemic disease is suspected:
- Fungal culture: only if scalp inflammation or scaling suggests tinea capitis 1, 2
- Skin biopsy: reserved for uncertain diagnosis or suspected scarring alopecia 1, 2
- Serum ferritin: if iron deficiency suspected (optimal ≥60 ng/mL needed for hair growth) 2
- TSH and free T4: if thyroid disease suspected 2
- Total testosterone, free testosterone, SHBG: only if signs of androgen excess (acne, hirsutism, irregular periods) 2
Common pitfall: Ordering extensive autoimmune panels in straightforward alopecia areata is unnecessary, as the modest increase in autoimmune disease prevalence does not justify routine screening 1, 2
First-Line Management by Diagnosis
Limited Patchy Alopecia Areata (≤5 patches, each ≤3 cm)
Watchful waiting with reassurance is the legitimate first-line approach, as 34-50% of patients recover within one year without treatment. 1, 2
- Counsel patients that regrowth cannot be expected within 3 months of any individual patch 1, 2
- No treatment alters the long-term course of alopecia areata, though some induce temporary regrowth 1, 2
If treatment is desired:
- Intralesional triamcinolone acetonide 5-10 mg/mL (0.05-0.1 mL per injection, administered monthly) yields regrowth in approximately 62% of patients, with effects lasting about 9 months (Strength of recommendation B, Quality III) 1, 2
- Inject just beneath the dermis in the upper subcutis; each 0.05-0.1 mL injection produces a tuft of hair growth about 0.5 cm in diameter 1
- Main limitation is patient discomfort; skin atrophy at injection sites is a consistent side-effect 1
Treatments to avoid:
- Potent topical corticosteroids lack convincing efficacy evidence 1, 2
- Dithranol and minoxidil lotion are widely prescribed but have no convincing evidence of effectiveness 1
Extensive Alopecia Areata (>50% scalp involvement, alopecia totalis/universalis)
Contact immunotherapy with diphenylcyclopropenone (DPCP) is the best-documented treatment but achieves cosmetically worthwhile regrowth in <50% of patients (Strength of recommendation C). 1, 2
- Requires multiple hospital visits over several months 1, 2
- Protocol: sensitize with 2% DPCP to small scalp area, then apply weekly starting at 0.001%, increasing concentration until mild dermatitis occurs 1
- Some temporary local inflammation but serious side-effects are rare 1
Wigs provide immediate cosmetic benefit and are often the most practical solution for extensive, longstanding disease (Strength of recommendation D). 1, 2
Treatments not recommended:
- Systemic corticosteroids and PUVA have potentially serious side-effects and inadequate efficacy evidence 1, 2
- Oral zinc and isoprinosine are ineffective in controlled trials 2
Androgenetic Alopecia
For men: Initiate combination therapy with oral finasteride 1 mg daily and topical minoxidil 5% solution twice daily, as this is the only FDA-approved approach proven to halt progression and stimulate regrowth. 2, 3
For women: Topical minoxidil 2% solution twice daily is first-line treatment, which arrests progression rather than stimulates regrowth. 2
- Treatment must be continuous to maintain results; stopping leads to resumed hair loss 2, 3
- Initial therapeutic response often takes 12-24 months 6
- Monitor response with standardized photographs 3
Adjunctive therapy:
- Platelet-rich plasma (PRP) injections show promise with increased hair density: 3-5 sessions at 1-month intervals, then maintenance every 6 months 2, 3
Telogen Effluvium
Removal of the precipitating trigger (stress, nutritional deficiency, illness) leads to spontaneous remission in up to 80% of cases with short duration (<1 year). 1, 2
Tinea Capitis
Systemic oral antifungal therapy is required; fungal culture must be obtained before initiating treatment. 2
Critical Pitfalls to Avoid
- Do not confuse trichotillomania with alopecia areata: trichotillomania shows broken hairs firmly anchored in anagen, whereas alopecia areata displays exclamation-mark hairs 1, 2
- Failing to address psychological impact: hair loss can cause considerable psychological and social disability; patients with low self-esteem or work/social difficulties should be considered for mental-health referral 1, 2
- Starting aggressive treatments in children: intralesional steroids are often poorly tolerated and many clinicians are reluctant to use contact immunotherapy in pediatric patients 1