{
  "schemaVersion": 2,
  "eyebrow": "Dermatology",
  "title": "Alopecia Areata",
  "summary": "Confirm nonscarring alopecia areata clinically and with trichoscopy, exclude infectious or inflammatory mimics when indicated, quantify scalp loss with SALT, and match localized disease to intralesional corticosteroids versus FDA-approved oral JAK inhibition for severe disease.",
  "seoDescription": "Physician guide to alopecia areata diagnosis, trichoscopy, targeted laboratory testing, SALT assessment, corticosteroid injections, and JAK inhibitors.",
  "clinicalQuestion": "How should physicians diagnose, stage, and select treatment for localized versus severe alopecia areata?",
  "specialty": "Dermatology",
  "audience": "U.S. physicians and medical trainees",
  "tags": [
    "alopecia areata",
    "SALT score",
    "trichoscopy",
    "intralesional triamcinolone",
    "baricitinib",
    "ritlecitinib",
    "JAK inhibitor"
  ],
  "keyTakeaways": [
    "Use scalp examination and trichoscopy to establish a nonscarring alopecia pattern; yellow dots are a characteristic trichoscopic finding in alopecia areata. [1]",
    "Record baseline Severity of Alopecia Tool (SALT) score to quantify scalp involvement and assess response longitudinally. [13]",
    "For active localized disease, intralesional triamcinolone acetonide is a first-line option; published consensus dosing is 2.5-10 mg/mL, with 10-20 mg maximum per session every 2-6 weeks. [18]",
    "Consider FDA-approved oral JAK inhibition for severe disease: baricitinib for adults and ritlecitinib for patients aged 12 years or older. [16][18]",
    "Laboratory testing should be targeted to diagnostic mimics, clinical suspicion of autoimmune comorbidity, and baseline or follow-up requirements for systemic treatment rather than performed reflexively in every patient. [9][11]"
  ],
  "sections": [
    {
      "id": "confirm-the-diagnosis",
      "eyebrow": "Initial assessment",
      "heading": "Confirm alopecia areata and identify diagnoses that change management",
      "intro": "Prioritize exclusion of scarring alopecia and infectious mimics before immunosuppression.",
      "paragraphs": [
        "Document distribution, extent, activity, eyebrow/eyelash and body-hair involvement, nail findings, and scalp symptoms. Alopecia areata is a nonscarring autoimmune alopecia; preservation of follicular openings supports this branch, whereas inflammatory follicular lesions, scale, or a clinically unexpected course should prompt reconsideration of infection, lupus erythematosus, lichen planopilaris, or another cicatricial alopecia. [7][16]",
        "Perform trichoscopy at the alopecic patch and active edge when the clinical diagnosis is uncertain. Yellow dots are characteristic of alopecia areata. Trichoscopy can also direct biopsy selection when lesions are follicular, atypical, or fail expected treatment, although overlapping dermoscopic findings prevent reliance on a single sign to exclude other scalp disorders. [1][6]",
        "Biopsy an active, representative lesion when scarring alopecia, cutaneous lupus, lichen planopilaris, folliculotropic mycosis fungoides, or another mimic remains plausible after examination and trichoscopy. Dermoscopy-guided biopsy is particularly useful for follicular lesions behaving unexpectedly or not responding to treatment. [6][24]"
      ],
      "bullets": [
        "Evaluate for tinea capitis, secondary syphilis, and lupus when morphology, symptoms, exposure history, or systemic findings suggest these mimics; each changes treatment away from alopecia-directed immunotherapy. [9]",
        "Do not interpret nonspecific vitamin, iron, or zinc abnormalities as proof of alopecia areata causation; expert testing practices vary substantially for potentially contributory abnormalities. [9][11]"
      ],
      "subsections": [],
      "table": {
        "caption": "Diagnostic branch points in patchy scalp alopecia. [1][6][9][24]",
        "columns": [
          "Finding",
          "Interpretation",
          "Next action"
        ],
        "rows": [
          [
            "Nonscarring patch with yellow dots on trichoscopy",
            "Supports alopecia areata. [1]",
            "Stage extent with SALT and select treatment by disease burden and patient goals. [13]"
          ],
          [
            "Scale, inflammatory follicular lesions, or clinical concern for infection",
            "Consider tinea capitis or other infectious follicular disease. [6][9]",
            "Pursue infection-directed evaluation before systemic immunomodulation. [9]"
          ],
          [
            "Loss of follicular ostia, perifollicular inflammatory change, or atypical persistent plaques",
            "Raises concern for cicatricial alopecia, lupus, lichen planopilaris, or folliculotropic mycosis fungoides. [6][24]",
            "Use trichoscopy to choose an active biopsy site. [6]"
          ],
          [
            "Unexpected course or no meaningful response to the presumed diagnosis",
            "Diagnostic reassessment is required because trichoscopic patterns overlap among follicular diseases. [6]",
            "Repeat examination and obtain a dermoscopy-guided biopsy when appropriate. [6]"
          ]
        ]
      }
    },
    {
      "id": "stage-and-risk-stratify",
      "eyebrow": "Disease burden",
      "heading": "Quantify severity and recognize patterns associated with greater treatment need",
      "intro": "Use a reproducible baseline measure before treating and at follow-up.",
      "paragraphs": [
        "Calculate and record the Severity of Alopecia Tool score at baseline; SALT has been validated for alopecia areata trials and routine practice. Use serial SALT measurements rather than an unstructured impression of density to determine whether localized therapy is adequate or whether severe disease warrants systemic discussion. [13]",
        "Classify complete scalp hair loss clinically as alopecia totalis and complete scalp and body hair loss as alopecia universalis. These phenotypes begin with SALT 100 and are represented among patients treated with ritlecitinib in long-term studies; severe baseline burden should prompt early discussion of systemic options rather than prolonged cycles of painful focal injections. [12]",
        "Ask directly about functional and psychosocial impact, including anxiety, depression symptoms, concealment burden, and occupational or social impairment. Alopecia areata is associated with lower quality of life and psychiatric comorbidity, and structured assessment can change the urgency of treatment escalation and behavioral-health referral. [7][14][21]"
      ],
      "bullets": [
        "Photograph scalp, brows, and lashes at baseline under consistent conditions to complement serial SALT assessment. [13]",
        "Reassess active disease and regrowth after each intralesional treatment cycle; historical reports describe regrowth within 4-6 weeks, but continued treatment for 3-4 months was needed in some patients. [3]",
        "Discuss that long-standing extensive disease may have a lower likelihood of satisfactory response than mild patchy disease; observational long-term data associate severe totalis/universalis patterns with poorer outcomes. [15]"
      ],
      "subsections": [],
      "table": {
        "caption": "Severity-directed treatment framing. [12][13][18]",
        "columns": [
          "Clinical pattern",
          "Measurement",
          "Treatment implication"
        ],
        "rows": [
          [
            "Limited patchy scalp involvement",
            "Baseline and serial SALT score; lesion photographs. [13]",
            "Localized intralesional triamcinolone is a first-line treatment option for active disease. [18]"
          ],
          [
            "Extensive scalp loss",
            "Serial SALT score to quantify burden and response. [13]",
            "Discuss systemic treatment options, including FDA-approved JAK inhibitors when disease is severe. [16][18]"
          ],
          [
            "Alopecia totalis or universalis",
            "SALT 100 at baseline in the clinical trial classification. [12]",
            "Prioritize counseling about lower response certainty and systemic therapy tradeoffs; focal injections alone are often impractical for large affected areas. [2][12]"
          ]
        ]
      }
    },
    {
      "id": "targeted-testing",
      "eyebrow": "Laboratory decisions",
      "heading": "Use targeted laboratory testing rather than an undifferentiated alopecia panel",
      "intro": "Testing should answer a specific diagnostic, comorbidity, or treatment-safety question.",
      "paragraphs": [
        "Order testing when it is triggered by a plausible mimic, symptoms or signs of an associated autoimmune disease, or intended systemic treatment. Expert consensus addresses laboratory evaluation in alopecia areata, but real-world testing remains variable and often extends to thyroid disease, coeliac disease, pernicious anemia, iron, zinc, and vitamin D assessment. [9][11]",
        "When secondary syphilis, tinea capitis, or lupus is clinically plausible, direct testing toward that alternative diagnosis rather than labeling the patient with alopecia areata on morphology alone. A positive mimic workup changes treatment selection and may preclude or defer immunosuppressive therapy. [9]",
        "Before prescribing a systemic JAK inhibitor, obtain the baseline and ongoing safety evaluation required for that drug and follow current U.S. product labeling. The literature identifies screening and monitoring for contraindications and adverse effects of JAK inhibitors as a distinct indication for laboratory testing in alopecia areata. [9]"
      ],
      "bullets": [
        "Use autoimmune testing selectively when history, examination, or symptoms suggest thyroid disease, coeliac disease, pernicious anemia, vitiligo, lupus, or another autoimmune condition. [9][16]",
        "Do not allow normal laboratory findings to override a convincing clinical and trichoscopic diagnosis; laboratory testing is principally used for mimics, associations, contributory factors, and systemic-therapy safety. [9][11]"
      ],
      "subsections": [],
      "table": {
        "caption": "Laboratory testing should be linked to the clinical question. [9][11]",
        "columns": [
          "Clinical trigger",
          "Testing purpose",
          "Result changes"
        ],
        "rows": [
          [
            "Morphology or history suggests tinea capitis, secondary syphilis, or lupus",
            "Evaluate an infectious or inflammatory mimic. [9]",
            "Treat the alternative diagnosis rather than escalating alopecia areata therapy. [9]"
          ],
          [
            "Symptoms or signs suggest autoimmune comorbidity",
            "Assess thyroid disease, coeliac disease, pernicious anemia, or another suspected autoimmune condition. [9]",
            "Initiate disease-specific evaluation or co-management if confirmed. [9]"
          ],
          [
            "Considering or receiving a JAK inhibitor",
            "Screen and monitor for systemic-treatment contraindications or adverse effects. [9]",
            "Determine eligibility and whether treatment can be continued safely. [9]"
          ]
        ]
      }
    },
    {
      "id": "localized-treatment",
      "eyebrow": "Localized disease",
      "heading": "Treat active limited alopecia areata with intralesional corticosteroids",
      "intro": "Use focal injection therapy when affected area and patient tolerance make local treatment practical.",
      "paragraphs": [
        "For active patchy alopecia areata, intralesional triamcinolone acetonide is regarded as first-line treatment. Use concentrations of 2.5-10 mg/mL, limit total dose to 10-20 mg per session, and repeat at 2-6-week intervals. The cited consensus identifies 10 mg/mL on the scalp as producing an optimal response with acceptable adverse reactions, but concentration and cumulative exposure should be individualized to site and atrophy risk. [18]",
        "Assess for regrowth and local toxicity at each visit. Pain, bleeding, headache, systemic absorption, dyschromia, and reversible local cutaneous atrophy are recognized adverse effects; repeated injections may also produce transient rather than durable responses. [2][18]",
        "Stop a nonresponsive injection strategy after 6 months and reassess the diagnosis, disease extent, treatment feasibility, and systemic options. This threshold also prevents indefinite exposure to injection pain and local atrophy in a patient who is unlikely to benefit from continued focal treatment. [18]"
      ],
      "bullets": [
        "Avoid using intralesional treatment as the sole strategy for very large areas when repeated injections become painful or impractical. [2]",
        "Topical corticosteroids may be used in practice, but evidence summarized in an evidence-based review characterizes topical and intralesional corticosteroids as moderately effective short-term treatments for patchy disease. [17]",
        "Explain that topical corticosteroids and topical macrolide immunomodulators may have limited efficacy because of insufficient penetration to the hair bulb. [2]"
      ],
      "subsections": [],
      "table": {
        "caption": "Intralesional triamcinolone treatment parameters for active alopecia areata. [18]",
        "columns": [
          "Parameter",
          "Practical specification",
          "Decision point"
        ],
        "rows": [
          [
            "Agent",
            "Triamcinolone acetonide. [18]",
            "Use for active localized alopecia areata. [18]"
          ],
          [
            "Concentration",
            "2.5-10 mg/mL; 10 mg/mL is reported as optimal for scalp response with acceptable adverse reactions. [18]",
            "Use lower exposure where local atrophy risk is a concern. [18]"
          ],
          [
            "Maximum session dose",
            "10-20 mg. [18]",
            "Do not exceed the cited session range. [18]"
          ],
          [
            "Interval",
            "Every 2-6 weeks. [18]",
            "Assess regrowth and adverse effects before reinjection. [18]"
          ],
          [
            "Stopping rule",
            "Discontinue if no improvement within 6 months. [18]",
            "Reassess diagnosis and escalate or change treatment strategy. [18]"
          ]
        ]
      }
    },
    {
      "id": "severe-disease-systemic-therapy",
      "eyebrow": "Severe disease",
      "heading": "Use FDA-approved JAK inhibitors when severe alopecia areata warrants systemic treatment",
      "intro": "Select systemic therapy by age, severity, patient priorities, and safety eligibility.",
      "paragraphs": [
        "For adults with severe alopecia areata, baricitinib is FDA approved. In the BRAVE-AA1 and BRAVE-AA2 phase 3 trials, SALT scores of 20 or less at week 52 occurred in 40.9% and 21.2% of patients receiving 4 mg and 2 mg, respectively, in BRAVE-AA1 and in 36.8% and 24.4%, respectively, in BRAVE-AA2. These results support expectation-setting: meaningful scalp regrowth occurs in a subset, not all treated patients. [7][16]",
        "For severe alopecia areata in patients aged 12 years or older, ritlecitinib is an FDA-approved option. In ALLEGRO, 23% receiving ritlecitinib 50 mg achieved SALT 20 or less at week 24 versus 1.5% with placebo; continued daily 50-mg treatment was associated with progressive improvement in SALT distribution through 24 months. [7][12][18]",
        "Use current U.S. prescribing information for agent-specific contraindications, pretreatment screening, dose modification, and adverse-effect monitoring. Do not substitute off-label JAK inhibitors or conventional systemic immunosuppressants for an approved agent without documenting the rationale, because evidence quality and optimal dosing for agents such as methotrexate and sulfasalazine remain limited. [9][15]"
      ],
      "bullets": [
        "Choose baricitinib only for adults with severe disease; its FDA approval for severe alopecia areata dates to 2022. [16]",
        "Ritlecitinib provides an approved systemic option beginning at age 12 years for severe disease. [7][18]",
        "Frame response using serial SALT rather than photographs alone; the key trial outcome was SALT 20 or less. [7][12][13]",
        "Avoid relying on systemic cyclosporine as a routine equivalent to approved JAK therapy; small case series reported cosmetically acceptable results in only 25%-50% and systemic toxicity constrains use. [2]"
      ],
      "subsections": [],
      "table": {
        "caption": "FDA-approved systemic JAK inhibitor evidence for severe alopecia areata. [7][12][16][18]",
        "columns": [
          "Agent",
          "Eligible population",
          "Efficacy benchmark",
          "Clinical use"
        ],
        "rows": [
          [
            "Baricitinib",
            "Adults with severe alopecia areata. [16][18]",
            "SALT ≤20 at week 52: 40.9% with 4 mg and 21.2% with 2 mg in BRAVE-AA1; 36.8% and 24.4%, respectively, in BRAVE-AA2. [7]",
            "Discuss expected benefit, safety screening, monitoring, and need for serial SALT assessment. [7][9][13]"
          ],
          [
            "Ritlecitinib",
            "Patients aged ≥12 years with severe alopecia areata. [7][18]",
            "Ritlecitinib 50 mg: SALT ≤20 at week 24 in 23% versus 1.5% with placebo in ALLEGRO. [7]",
            "Use daily 50 mg as studied; follow current U.S. labeling for safety management. [12][9]"
          ]
        ]
      }
    },
    {
      "id": "follow-up-and-escalation",
      "eyebrow": "Monitoring",
      "heading": "Monitor response, toxicity, and diagnostic fidelity",
      "intro": "Follow-up should have a predefined measurement and an escalation trigger.",
      "paragraphs": [
        "At each follow-up, repeat SALT scoring, compare standardized photographs, inspect for active new patches and regrowth, and document local adverse effects when injections are used. For systemic therapy, incorporate the treatment-specific safety monitoring required by current labeling alongside clinical response assessment. [9][13][18]",
        "Escalate from local to systemic discussion when disease is extensive, totalis/universalis is present, injections are impractical, patient burden is high, or there is no improvement after 6 months of intralesional therapy. Re-biopsy rather than merely escalating immunosuppression if the morphology becomes inflammatory, follicular, scarring, or otherwise discordant with alopecia areata. [6][18]",
        "Include mental-health screening and referral when distress, anxiety, depression symptoms, or impaired function is identified. Psychiatric comorbidity and reduced quality of life are documented in alopecia areata and should be managed as treatment-relevant disease burden rather than an incidental reaction to cosmetic change. [7][14][21]"
      ],
      "bullets": [
        "Local injection toxicity: look specifically for cutaneous atrophy and dyschromia before reinjection. [18]",
        "Systemic-treatment monitoring: follow the selected JAK inhibitor's current U.S. labeling and laboratory safety requirements. [9]",
        "Diagnostic failure trigger: unexpected lesions or failure to respond should prompt trichoscopy-guided biopsy consideration. [6]"
      ],
      "subsections": [],
      "table": {
        "caption": "Follow-up actions by treatment pathway. [6][9][13][18]",
        "columns": [
          "Pathway",
          "Monitor",
          "Escalate or change course when"
        ],
        "rows": [
          [
            "Intralesional triamcinolone",
            "SALT, regrowth, pain, bleeding, dyschromia, and local atrophy at treatment visits. [13][18]",
            "No improvement by 6 months, clinically meaningful toxicity, or disease becomes too extensive for practical injection treatment. [18][2]"
          ],
          [
            "Oral JAK inhibitor",
            "Serial SALT plus agent-specific safety testing and adverse effects per current labeling. [9][13]",
            "Safety evaluation changes eligibility or response and patient priorities no longer justify ongoing systemic exposure. [9]"
          ],
          [
            "Atypical or refractory presentation",
            "Clinical morphology and trichoscopic findings. [6]",
            "Obtain a dermoscopy-guided biopsy when mimic or scarring process remains a concern. [6][24]"
          ]
        ]
      }
    }
  ],
  "faq": [],
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  "citations": [
    {
      "number": 1,
      "title": "Reflectance Confocal Microscopy of the Yellow Dot Pattern in ...",
      "detail": "jamanetwork.com",
      "url": "https://jamanetwork.com/journals/jamadermatology/fullarticle/426451",
      "authors": "jamanetwork.com",
      "host": "jamanetwork.com",
      "snippet": "The presence of yellow dots is a characteristic dermoscopic finding in alopecia areata. scalp dermoscopy, s showed the yellow dot pattern in",
      "score": 0.3701121
    },
    {
      "number": 2,
      "title": "Alefacept for Alopecia Areata",
      "detail": "jamanetwork.com",
      "url": "https://jamanetwork.com/journals/jamadermatology/fullarticle/401021",
      "authors": "jamanetwork.com",
      "host": "jamanetwork.com",
      "snippet": "Title: Alefacept for Alopecia Areata\nImage 4: Posterior scalp of patient 3 at 15-week follow-up demonstrating extensive regrowth of terminal hair. Posterior scalp of patient 3 at 15-week follow-up demonstrating extensive regrowth of terminal hair. For the next 9 years, the patient received intralesi",
      "score": 0.6786044
    },
    {
      "number": 3,
      "title": "Alopecia Areata - JAMA Network",
      "detail": "jamanetwork.com",
      "url": "https://jamanetwork.com/journals/DERM/articlepdf/554546/archderm_128_11_016.pdf",
      "authors": "jamanetwork.com",
      "host": "jamanetwork.com",
      "snippet": "alopecia areata treated with intralesional triamcinolone ace- tonide. Regrowth, within 4 to 6 weeks. Continuous treatment for 3 to 4 months was necessary for",
      "score": 0.5232017
    },
    {
      "number": 4,
      "title": "Selectivity, efficacy and safety of JAKinibs: new evidence for a still ...",
      "detail": "ard.bmj.com",
      "url": "https://ard.bmj.com/content/83/2/139",
      "authors": "ard.bmj.com",
      "host": "ard.bmj.com",
      "snippet": ". Topical Janus kinase inhibitors for the treatment of pediatric Alopecia Areata. J Am Acad Dermatol 2017;77:167–70. doi:10.1016/j.jaad.2017.03.024pmid:28619556\n\nOpenUrlPubMed\n\n187.   ↵\n\n    2.   Bissonnette R, \n    3.   Papp KA, \n    4.   Poulin Y, et al\n\n. Topical tofacitinib for Atopic dermatitis",
      "score": 0.5737984
    },
    {
      "number": 5,
      "title": "Trichoscopy criteria for diagnosing female androgenic alopecia.",
      "detail": "www.nature.com",
      "url": "https://www.nature.com/articles/npre.2008.1913.1.pdf",
      "authors": "www.nature.com",
      "host": "www.nature.com",
      "snippet": "which over time may become cosmetically unacceptable and psychologically frustrating.4 Differences in natural history, prognosis and emerging new therapeutic possibilities 5 make differential diagnosis and early diagnosis of FAGA especially important. Currently the diagnosis of FAGA is usually based",
      "score": 0.49348235
    },
    {
      "number": 6,
      "title": "Clinical and trichoscopic features in 18 cases of Folliculotropic Mycosis Fungoides with scalp involvement | Scientific Reports",
      "detail": "www.nature.com",
      "url": "https://www.nature.com/articles/s41598-021-90168-9",
      "authors": "www.nature.com",
      "host": "www.nature.com",
      "snippet": "involving the scalp examined in two dermatology tertiary referral centres. The identification of specific dermoscopic patterns could be helpful in the differential diagnosis with other dermatoses with scalp involvement and alopecia (lupus, lichen planopilaris, alopecia areata) together with the foll",
      "score": 0.46570396
    },
    {
      "number": 7,
      "title": "‌Global burden of alopecia areata from 1990 to 2019 and emerging treatment trends analyzed through GBD 2019 and bibliometric data | Scientific Reports",
      "detail": "www.nature.com",
      "url": "https://www.nature.com/articles/s41598-025-07224-x",
      "authors": "www.nature.com",
      "host": "www.nature.com",
      "snippet": "(2022).\"). Based on these findings, as of June 2022, both the EMA and FDA have granted approval for a JAKis as the first and currently sole labeled therapy for adult AA. In the two subsequent Phase III trials (BRAVE-AA1 and BRAVE-AA2), patients treated with Baricitinib at doses of 4 mg and 2 mg, res",
      "score": 0.3584434
    },
    {
      "number": 8,
      "title": "Alopecia areata | Nature Reviews Disease Primers",
      "detail": "www.nature.com",
      "url": "https://www.nature.com/articles/s41572-025-00664-9",
      "authors": "www.nature.com",
      "host": "www.nature.com",
      "snippet": "# Alopecia areata. Demographic and clinical features of 1,641 patients with alopecia areata, alopecia totalis, and alopecia universalis: a single-center retrospective study. Prevalence, comorbidities, and treatment patterns of Japanese patients with alopecia areata: a descriptive study using Japan m",
      "score": 0.70287734
    },
    {
      "number": 9,
      "title": "COLLAB: A Global Survey of Clinical and Laboratory Assessment in Alopecia Areata by Hair Specialists - O'Connor - 2025 - JEADV Clinical Practice - Wiley Online Library",
      "detail": "onlinelibrary.wiley.com",
      "url": "https://onlinelibrary.wiley.com/doi/full/10.1002/jvc2.70067",
      "authors": "onlinelibrary.wiley.com",
      "host": "onlinelibrary.wiley.com",
      "snippet": "Thirty hair experts from 14 countries and six continents contributed to develop a 24-item survey collecting demographic information on respondents; methods of severity assessment; and laboratory testing practices in AA for mimics, contributory factors, associations, and workup for systemic therapy. ",
      "score": 0.5815176
    },
    {
      "number": 10,
      "title": "Trichoscopy pattern and evaluation of serum vitamin D status in alopecia areata - ScienceDirect",
      "detail": "www.sciencedirect.com",
      "url": "https://www.sciencedirect.com/science/article/abs/pii/S1572100023002387",
      "authors": "www.sciencedirect.com",
      "host": "www.sciencedirect.com",
      "snippet": "### Trichoscopy: a new method for diagnosing hair loss\n\n### J. Drugs Dermatol.\n\n### Clinical significance of trichoscopy in common causes of hair loss in children: analysis of 134 cases\n\n### Int. J. Trichol.\n\n### Investigative guidelines for alopecia areata\n\n### Dermatol. Ther.\n\n### Comparison of vi",
      "score": 0.51662046
    },
    {
      "number": 11,
      "title": "The Alopecia Areata Consensus of Experts (ACE) study part II: Results of an international expert opinion on diagnosis and laboratory evaluation for alopecia areata - ScienceDirect",
      "detail": "www.sciencedirect.com",
      "url": "https://www.sciencedirect.com/science/article/pii/S0190962220326141",
      "authors": "www.sciencedirect.com",
      "host": "www.sciencedirect.com",
      "snippet": "Title: The Alopecia Areata Consensus of Experts (ACE) study part II: Results of an international expert opinion on diagnosis and laboratory evaluation for alopecia areata - ScienceDirect\n# Original article The Alopecia Areata Consensus of Experts (ACE) study part II: Results of an international expe",
      "score": 0.5041753
    },
    {
      "number": 12,
      "title": "SALT score distribution with ritlecitinib treatment up to 24 months in alopecia areata - Reguiai - Journal of the European Academy of Dermatology and Venereology - Wiley Online Library",
      "detail": "onlinelibrary.wiley.com",
      "url": "https://onlinelibrary.wiley.com/doi/10.1111/jdv.20698",
      "authors": "onlinelibrary.wiley.com",
      "host": "onlinelibrary.wiley.com",
      "snippet": "# SALT score distribution with ritlecitinib treatment up to 24 months in alopecia areata. **SALT score distribution for participants who received daily ritlecitinib 50 mg without a loading dose in ALLEGRO-2b/3 and ALLEGRO-LT.**. Ritlecitinib, an oral JAK3/TEC family kinase inhibitor, demonstrated ef",
      "score": 0.49919498
    },
    {
      "number": 13,
      "title": "Objective outcome measures: Collecting meaningful data on alopecia areata - ScienceDirect",
      "detail": "www.sciencedirect.com",
      "url": "https://www.sciencedirect.com/science/article/abs/pii/S0190962217326142",
      "authors": "www.sciencedirect.com",
      "host": "www.sciencedirect.com",
      "snippet": "### J Am Acad Dermatol\n\n### Ringworm and Alopecia Areata. Their Pathology, Diagnosis and Treatment\n\n### Evaluation of disturbed hair growth in alopecia areata and other alopecias\n\n### Ann N Y Acad Sci\n\n### Clinical tools for assessing hair loss\n\n### Exclamation marks and other trichoscopic signs of ",
      "score": 0.49157855
    },
    {
      "number": 14,
      "title": "Lifetime prevalence of psychiatric disorders in patients with alopecia areata - ScienceDirect",
      "detail": "www.sciencedirect.com",
      "url": "https://www.sciencedirect.com/science/article/pii/0010440X9190045E",
      "authors": "www.sciencedirect.com",
      "host": "www.sciencedirect.com",
      "snippet": "# Lifetime prevalence of psychiatric disorders in patients with alopecia areata. Thirty-one patients with alopecia areata were administered a structured psychiatric interview (the Diagnostic Interview Schedule; DIS). Patients with patchy alopecia areata were more likely to have a diagnosis of genera",
      "score": 0.3699755
    },
    {
      "number": 15,
      "title": "Real-world evidence in alopecia areata treatment:... : Dermatologica Sinica",
      "detail": "journals.lww.com",
      "url": "https://journals.lww.com/ders/fulltext/2026/01000/real_world_evidence_in_alopecia_areata_treatment_.3.aspx",
      "authors": "journals.lww.com",
      "host": "journals.lww.com",
      "snippet": "Title: Real-world evidence in alopecia areata treatment:... : Dermatologica Sinica\nTraditional treatments like such as corticosteroids, systemic immunosuppressives, and contact immunotherapy are commonly used but are often associated with high relapse rates and inconsistent efficacy. Off-label medic",
      "score": 0.8058924
    },
    {
      "number": 16,
      "title": "Dual improvement of alopecia areata and immune thrombocytopenia with baricitinib: a case report | Skin Health and Disease | Oxford Academic",
      "detail": "academic.oup.com",
      "url": "https://academic.oup.com/skinhd/article/5/1/66/7972527",
      "authors": "academic.oup.com",
      "host": "academic.oup.com",
      "snippet": "The oral Janus kinase (JAK) inhibitor baricitinib is approved by the U.S. Food and Drug Administration for the treatment of alopecia areata (AA). We report a case of dual improvement of AA and immune thrombocytopenia (ITP) with oral baricitinib monotherapy, which may suggest linked autoimmune pathop",
      "score": 0.76951396
    },
    {
      "number": 17,
      "title": "What is the most effective treatment for alopecia areata? - Ovid",
      "detail": "journals.lww.com",
      "url": "https://journals.lww.com/ebp/fulltext/2015/05000/what_is_the_most_effective_treatment_for_alopecia.17.aspx",
      "authors": "journals.lww.com",
      "host": "journals.lww.com",
      "snippet": "Intralesional and topical corticosteroids are moderately effective in the short term (12 weeks) for patchy hair loss in alopecia areata.",
      "score": 0.55796635
    },
    {
      "number": 18,
      "title": "Taiwanese Dermatological Association consensus on... : Dermatologica Sinica",
      "detail": "journals.lww.com",
      "url": "https://journals.lww.com/ders/_layouts/15/oaks.journals/downloadpdf.aspx?an=00701581-202501000-00004",
      "authors": "journals.lww.com",
      "host": "journals.lww.com",
      "snippet": "Intralesional corticosteroid injection is regarded as the first-line treatment for patients with active AA.[23][41][43][47] The most commonly used corticosteroid is triamcinolone acetonide (TA), typically prepared at a concentration of 2.5–10 mg/mL, with a maximum dose of 10–20 mg per treatment session",
      "score": 0.46687052
    },
    {
      "number": 19,
      "title": "A Comprehensive Overview on Alopecia Areata with Review on ...",
      "detail": "journals.lww.com",
      "url": "https://journals.lww.com/ijd/_layouts/15/oaks.journals/downloadpdf.aspx?an=00076423-990000000-00329",
      "authors": "journals.lww.com",
      "host": "journals.lww.com",
      "snippet": "Various treatment options, including corticosteroids, immunotherapy, and emerging biologic therapies, aim to manage symptoms and promote hair regrowth, but",
      "score": 0.45304462
    },
    {
      "number": 20,
      "title": "Comparison of Current International Guidelines for the Management of Alopecia Areata—Comprehensive Review",
      "detail": "pmc.ncbi.nlm.nih.gov",
      "url": "https://pmc.ncbi.nlm.nih.gov/articles/PMC12429261",
      "authors": "pmc.ncbi.nlm.nih.gov",
      "host": "pmc.ncbi.nlm.nih.gov",
      "snippet": "97..Messenger A.G., McKillop J., Farrant P., McDonagh A., Sladden M., Hughes J., McLelland J., Punjabi S., Buckley D., Nasr I., _et al_. British Association of Dermatologists’ guidelines for the management of alopecia areata 2012. _Br. J. Dermatol._. 2012. 166:916-926. doi: 10.1111/j.1365-2133.2012.",
      "score": 0.72254705
    },
    {
      "number": 21,
      "title": "Alopecia Areata: Pathogenesis, Diagnosis, and Therapies",
      "detail": "pmc.ncbi.nlm.nih.gov",
      "url": "https://pmc.ncbi.nlm.nih.gov/articles/PMC12010142",
      "authors": "pmc.ncbi.nlm.nih.gov",
      "host": "pmc.ncbi.nlm.nih.gov",
      "snippet": "18. A. G. Messenger ,  J. McKillop ,  P. Farrant ,  A. J. McDonagh , and  M. Sladden , “British Association of Dermatologists' Guidelines for the Management of Alopecia Areata 2012,” _British Journal of Dermatology_ 166, no. 5 (2012): 916–926. doi: 10.1111/j.1365-2133.2012.10955.x  [DOI] [PubMed] [G",
      "score": 0.7156829
    },
    {
      "number": 22,
      "title": "Interventions for alopecia areata",
      "detail": "pmc.ncbi.nlm.nih.gov",
      "url": "https://pmc.ncbi.nlm.nih.gov/articles/PMC13287352",
      "authors": "pmc.ncbi.nlm.nih.gov",
      "host": "pmc.ncbi.nlm.nih.gov",
      "snippet": "#### Juni 2001\n\n1.   Juni P, Altman DG, Egger M. Assessing the quality of controlled clinical trials. BMJ 2001;323:42-6. [DOI] [PMC free article] [PubMed] [Google Scholar]\n\n#### MacDonald Hull 2003\n\n1.   MacDonald Hull SP, Wood ML, Hutchinson PE, Sladden M, Messenger AG, British Association of Derma",
      "score": 0.69697046
    },
    {
      "number": 23,
      "title": "Real World Evidence in Alopecia Areata: Current Management, Emerging Therapies and Future Challenges – A Narrative Review",
      "detail": "pmc.ncbi.nlm.nih.gov",
      "url": "https://pmc.ncbi.nlm.nih.gov/articles/PMC13264305",
      "authors": "pmc.ncbi.nlm.nih.gov",
      "host": "pmc.ncbi.nlm.nih.gov",
      "snippet": "29..Messenger AG, McKillop J, Farrant P, McDonagh AJ, Sladden M. British Association of Dermatologists’ guidelines for the management of alopecia areata 2012. _\\_Br J Dermatol\\__. 2012;166(5):916–926. doi: doi: 10.1111/j.1365-2133.2012.10955.x  [DOI] [PubMed] [Google Scholar]\n   30..Harries MJ, Ahme",
      "score": 0.6783488
    },
    {
      "number": 24,
      "title": "[PDF] Dermoscopy in selected disorders of scarring alopecia",
      "detail": "applications.emro.who.int",
      "url": "https://applications.emro.who.int/imemrf/J_Pak_Assoc_Dermatol/J_Pak_Assoc_Dermatol_2018_28_4_449_451.pdf",
      "authors": "applications.emro.who.int",
      "host": "applications.emro.who.int",
      "snippet": "Dermoscopy thus is helpful in differentiating LPP, DLE and PB and obviating the need of biopsy in all cases.",
      "score": 0.49553296
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  ],
  "publishedAt": "2026-09-15T23:13:06.607946+00:00",
  "updatedAt": "2026-09-15T23:13:06.607946+00:00",
  "readingMinutes": 6,
  "slug": "alopecia-areata"
}