Alopecia areata is a common non-scarring autoimmune hair loss disorder targeting hair follicles, resulting in sudden, smooth, localized patches of hair loss on the scalp or any hair-bearing site. Its course is relapsing and unpredictable.
1. Pattern and Timeline:
Onset: Sudden, over weeks, resulting in well-defined, smooth patches on the scalp. May involve the beard, eyebrows, or body hair.
Patterns: Most common is patchy. Less common but important patterns:
Alopecia Totalis: Loss of all scalp hair.
Alopecia Universalis: Loss of all body hair.
Ophiasis: Band-like loss along the occipital/temporal margins (poor prognosis).
Course: Many patients with patchy AA experience spontaneous regrowth within 12 months, but relapses are common.
2. Symptoms and Associated Features:
Sensation: Usually asymptomatic; some report mild tingling or tightness (trichodynia) in active patches.
Nails: Patients may notice fine pitting, ridging, or trachyonychia (rough sandpaper nails), which is a sign of more severe disease and a poor prognostic indicator.
Autoimmune History: Patients should be asked about personal or family history of Thyroid disease, Vitiligo, Atopic Dermatitis, or Lupus.
Crucial Note for Darker Skin Tones:
Differential Diagnosis: The disease pattern is the same, but you must rule out Traction Alopecia and Central Centrifugal Cicatricial Alopecia (CCCA), which are particularly common in people of African descent.
Psychosocial Impact: The emotional and psychological burden (anxiety, depression, social avoidance) is often greater where hair is culturally central to identity.
Image Sourced From Skin Sight
What will it look like? (Examination)
1. Scalp / Hair Examination:
Patches: Non-scarring, well-demarcated patches of hair loss. The skin within the patch is smooth and normal (not shiny or atrophic). Follicular openings are visible.
Pathognomonic Sign: Exclamation-mark hairs at the patch margins (hairs tapered proximally, thicker distally).
Hair Pull Test: A positive test (pulling >10% of grasped hairs away) at the margin indicates active disease.
2. Key Findings in Darker Skin Tones:
Regrowing Hair: Regrowing hairs may be hypopigmented or white, creating a high contrast against the surrounding pigmented skin.
Pigment Change: Look for hypopigmented streaks or patches left by prior intralesional steroid injections.
3. Excluding Scarring Alopecias (Essential in Darker Skin):
The absence of follicular openings or the presence of perifollicular scale, erythema, or hyperpigmentation suggests a scarring alopecia (like CCCA or Discoid Lupus) rather than AA.
Look closely for the central, circular spreading pattern typical of CCCA (usually on the crown/vertex) or the distinct hairline loss of Traction Alopecia.
How can you help? (Treatment)
Management involves controlling disease activity, minimizing treatment side effects, and providing crucial psychological support.
1. General Principles:
Prognosis: Counsel patients about the unpredictable course. Prognosis is worse with childhood onset, ophiasis pattern, or coexistent nail dystrophy.
Psychosocial Care: Screen for anxiety/depression. Provide camouflage options (wigs, hair fibres) and signpost to support organizations.
2. Mild to Moderate Disease (<50% Scalp):
First-line: Intralesional Corticosteroids (ILCS): Triamcinolone acetonide (2.5–10 mg/mL) injected into the dermis every 4–6 weeks. This has a high success rate (60–67% regrowth).
Adjunctive: Topical Minoxidil (5%) or potent topical steroids (e.g., Clobetasol) for needle-averse patients.
3. Severe or Extensive Disease ( >50% Scalp, Totalis, Universalis):
Referral: These cases require specialist care.
Oral JAK Inhibitors: Medications like Baricitinib are now approved for severe AA, showing significant regrowth but require long-term monitoring for serious side effects (e.g., infections, VTE).
Topical Immunotherapy (Sensitization): Use of DPCP or SADBE to induce an allergic contact dermatitis.
Darker Skin Tones – Specific Treatment Risks:
ILCS Technique: Use the lowest effective concentration and ensure shallow injections to reduce the risk of local atrophy and hypopigmentation, which is highly visible and distressing.
Immunotherapy: Topical immunotherapy can cause hypo- and hyperpigmentation that must be carefully discussed, as the color change can be highly visible.
Hair Practices: Advise low-tension styles and cautious use of chemical relaxers to prevent traction damage that can mimic or worsen AA.
Sources
DermNet NZ – Alopecia Areata: https://dermnetnz.org/topics/alopecia-areata
StatPearls / NCBI Bookshelf – Alopecia Areata (2024 update): https://www.ncbi.nlm.nihim.gov/books/NBK537000/
The Pharmaceutical Journal – Common dermatological conditions in skin of colour (Belmo et al., 2021): https://pharmaceutical-journal.com/article/ld/common-dermatological-conditions-in-skin-of-colour
Skinsight – Alopecia Areata: https://skinsight.com/skin-conditions/alopecia-areata/