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Alopecia areata

Essential points for quick revision.

Synopsis

Recognise immune-mediated non-scarring hair loss, exclude infection and follicular destruction, grade extent and impact, and use topical or systemic treatment with realistic relapse and safety counselling.

  • Alopecia areata causes sharply defined smooth patches of non-scarring hair loss; follicular openings remain visible and the scalp is usually neither markedly inflamed nor scaly.
  • Exclamation-mark hairs, black dots, broken hairs, yellow dots and short tapered regrowth support active disease but no single dermoscopic feature is mandatory.
  • Examine eyebrows, eyelashes, beard, body hair and nails; pitting or rough trachyonychia supports the diagnosis and extensive loss changes prognosis and treatment eligibility.

Key red flags

Loss of follicular openings, scalp pain, perifollicular scale, pustules, boggy inflammation, a rapidly enlarging mass or systemic illness is not uncomplicated alopecia areata and requires urgent infection, scarring-alopecia or tumour assessment.

Follicular-destruction warning

Absent openings, perifollicular erythema or scale, pustules, pain and shiny atrophy point away from alopecia areata toward scarring disease.

Investigation priorities

01
Scalp, body-hair and nail examinationFirst step

Confirm non-scarring loss and measure anatomic extent beyond the reported patch.

Management branches

New limited patchConfirm non-scarring disease and agree a goal

One or a few smooth patches are present without infection or scarring features.

  1. Examine scalp, brows, lashes, body hair and nails, use trichoscopy where available and sample fungus only when scale or exposure supports it.
  2. Explain spontaneous regrowth, variable recurrence and prognostic factors, then offer observation, camouflage or a defined topical corticosteroid course according to age, site and preference.

Key medicines

Potent topical corticosteroid for limited scalp diseaseApply the prescribed scalp formulation thinly once daily for a defined course, commonly reviewed after six to twelve weeks before any continuation or break.
BaricitinibEligible adults take the specialist-selected oral dose once daily, usually 4 mg or 2 mg when age, risk, interactions or tolerability favour the lower dose.
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Sources and review status4 sources · checked 27 Aug 2026 · clinical review pending
Sources

Sources and review status

National guidance is shown before implementation-dependent detail. Typical adult dose examples remain subject to patient factors, contraindications and the live BNF or specialist protocol. Source check completed 27 Aug 2026; clinical approval remains outstanding.

Authoring stateRapid draftClinical stateAwaiting reviewJurisdictionUnited Kingdom