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A 23 yeat olf boy with ithcing and redness in scalp with hair shedding prev on prednisolone and metho trxate few years back the dr said disease has stopped but now the burning semsation and shedding reappears

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American Academy Dermatology scarring alopecia symptoms urgent dermatologist lichen planopilaris

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The symptoms are concerning for a return of an inflammatory scalp disease, particularly a type of scarring alopecia such as lichen planopilaris if that was his former diagnosis. Prednisolone and methotrexate are sometimes used when this condition is active.
Burning, itching, scalp redness, scaling around hairs, and renewed shedding can indicate active inflammation. In lichen planopilaris, burning, pain, or itching are often linked with active hair loss. - Dermatology, 2-Volume Set, 5e, p. 1404
He should see a dermatologist, ideally one who treats hair/scalp disorders, promptly, preferably within 1-2 weeks. The purpose is to stop further follicle damage, not just treat dandruff. A doctor may use scalp dermoscopy and, if needed, take a biopsy from the active red/scaly edge, not the smooth bald center. - Fitzpatrick's Dermatology, p. 1554
Important points:
  • Do not restart prednisolone or methotrexate on his own. Both need a diagnosis, monitoring, and prescription supervision.
  • Permanent regrowth is unlikely in areas where follicles have already been destroyed by scarring, but treating active inflammation can preserve remaining hair. - Fitzpatrick's Dermatology, p. 1555
  • Other possibilities must be ruled out, including seborrheic dermatitis, fungal scalp infection, bacterial folliculitis, discoid lupus, psoriasis, or non-scarring shedding.
  • Take photos of the scalp now and weekly in the same lighting. Bring old prescriptions, biopsy reports, and the name of the previous diagnosis to the appointment.
Seek same-day medical care if there are pus-filled bumps, crusting, fever, rapidly spreading painful redness, or swollen lymph nodes, as these can suggest infection.
I could not reliably assess the attached HEIC scalp photos in this chat because the image files could not be opened by the image-analysis service. The history alone, however, is enough to warrant prompt dermatology review. Recent treatment evidence for lichen planopilaris remains limited and specialist-directed, as reflected in a 2024 systematic review.

Treatment

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"lichen planopilaris" AND treatment

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lichen planopilaris treatment patient information diagnosis scalp biopsy

Treatment depends on confirming whether this is a relapse of lichen planopilaris or another scarring alopecia, versus dandruff, psoriasis, or a fungal/bacterial infection. Because he previously needed prednisolone and methotrexate, he should be assessed by a dermatologist before treatment is restarted.

What the dermatologist may use if inflammatory scarring alopecia is confirmed

  1. Anti-inflammatory scalp treatment
    • Strong prescription corticosteroid lotion/foam/solution for the scalp
    • Steroid injections into actively inflamed patches in some cases
    • Sometimes tacrolimus or pimecrolimus as a steroid-sparing topical treatment
  2. Oral treatment for active or spreading disease
    • Hydroxychloroquine or doxycycline are commonly considered initial systemic options.
    • If disease is more severe, progressive, or resistant, a specialist may consider methotrexate, mycophenolate, ciclosporin, retinoids, or a short supervised course of oral corticosteroid.
    • The aim is to stop burning, redness, itching, and further permanent follicle damage. It cannot reliably regrow hair from smooth, scarred areas where follicles are already gone. - Dermatology, 2-Volume Set, 5e, p. 1404
  3. Hair-growth support
    • Topical minoxidil can sometimes help the remaining viable follicles and may be used as an add-on, but it does not control the inflammation or cure scarring alopecia.
    • Do not rely on minoxidil alone if the scalp is burning, red, or actively shedding.
  4. Rule out infection before immunosuppressants
    • The dermatologist may perform dermoscopy, fungal testing/culture, and possibly a scalp biopsy from the red, scaly, hair-bearing edge. Treating an undiagnosed fungal infection with steroids or methotrexate can make it worse. A biopsy from an active margin is preferred in suspected scarring alopecia. - Fitzpatrick's Dermatology, p. 1554

Until he is seen

  • Do not restart old prednisolone or methotrexate without a dermatologist. Methotrexate requires blood monitoring and folic-acid planning; steroids can mask infection and have important adverse effects.
  • Avoid hair oils, harsh anti-dandruff products, chemical treatments, hair dye, scratching, tight headwear, and hot hair drying on inflamed areas.
  • Use a gentle fragrance-free shampoo. If there is obvious greasy flaking, a clinician may suggest an antifungal shampoo, but that does not replace evaluation for scarring alopecia.
  • Take clear weekly photos of the same scalp areas.
  • Bring previous biopsy reports and old prescriptions. Knowing the exact former diagnosis changes treatment.
Arrange a dermatology visit within 1-2 weeks, or sooner if there is rapidly expanding hair loss, pain, pus/crusting, fever, or boggy swollen areas. The DermNet treatment overview similarly emphasizes confirming activity with scalp examination or biopsy and using specialist-directed anti-inflammatory treatment.

Whats the mehotrexate dosw for scarring alopecia perticulary lpp

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lichen planopilaris methotrexate dose monitoring guideline

For lichen planopilaris (LPP), published dermatology experience commonly uses methotrexate 15 to 20 mg once weekly. - Fitzpatrick's Dermatology, systemic therapies section
It is never taken daily for LPP. A daily dosing error can cause life-threatening bone-marrow suppression, severe mouth ulcers, liver injury, and infection.
For this 23-year-old, the actual starting dose and route must be chosen by a dermatologist after confirming active LPP and checking for infection. A specialist may start lower and increase based on response, body factors, kidney/liver function, prior tolerance, and blood tests. Treatment often also includes prescription anti-inflammatory scalp therapy.
Before and during methotrexate, clinicians typically arrange:
  • Baseline CBC/platelets, liver tests, kidney function, hepatitis B/C and other infection-risk assessment as indicated
  • Regular CBC, liver and renal tests, especially after starting or changing dose
  • Folic acid supplementation, prescribed separately
  • Review of alcohol use, other medicines, vaccinations, and pregnancy/fertility counseling where relevant
He should not restart leftover methotrexate from an old prescription, even at his former dose, until the dermatologist has examined the scalp and reviewed current blood tests. LPP can resemble fungal scalp infection or other causes of hair loss, and immunosuppression would be unsafe if infection is present. The current evidence base for LPP treatments is limited and specialist-directed, as noted in this 2024 systematic review.

For how many days

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lichen planopilaris methotrexate treatment duration weeks

Methotrexate for LPP is usually prescribed in weeks to months, not for a fixed number of days.
  • A common initial assessment period is about 12 weeks.
  • Published LPP experience includes treatment courses of roughly 4 to 24 weeks.
  • If it is helping and blood tests are safe, the dermatologist may continue it for 6 months or longer, then reassess and reduce/stop gradually if the disease is inactive.
It is taken once a week only, never daily.
The exact duration depends on whether redness, burning, itching, shedding, and scalp inflammation have settled, plus regular CBC, liver, and kidney test results. Do not start, stop, or extend it without the prescribing dermatologist. - Fitzpatrick's Dermatology, systemic therapies section

I am a doctor so

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methotrexate dermatology monitoring guideline baseline CBC LFT renal folic acid weekly

Understood. For a confirmed active LPP relapse, a practical methotrexate course is generally:
  • MTX 15 mg once weekly orally or SC
  • Reassess clinically and trichoscopically at 12 weeks
  • Continue to 24 weeks (6 months) if there is improvement and safety labs remain acceptable
  • At 6 months, if symptoms, perifollicular erythema/scale, pull test, and photographic progression are quiet, decide whether to stop, taper, or continue a maintenance strategy based on relapse risk.
So, not “days”: the usual meaningful trial is 24 weekly doses, with an early assessment after 12 doses. Published LPP data include 15-20 mg weekly for 4-24 weeks. - Fitzpatrick's Dermatology, systemic therapies section
A concise regimen would be:
  • MTX 15 mg PO/SC weekly
  • Folic acid per local protocol, commonly 5 mg once weekly on a non-MTX day, or 1 mg daily except MTX day
  • Concurrent anti-inflammatory scalp therapy, such as potent topical steroid or intralesional triamcinolone for active margins
  • CBC, AST/ALT, albumin, creatinine/eGFR at baseline, then every 1-2 weeks during initiation/dose change, and every 2-3 months once stable, consistent with SPS methotrexate monitoring guidance
I would not judge efficacy by density alone at 12 weeks. In LPP, the principal endpoint is arrest of activity: burning/pruritus, perifollicular erythema and casts/scale, spread of patches, and pull-test positivity. Hair-density response is slower and scarred areas will not recover. The LPP evidence base remains limited, as summarized in this 2024 systematic review.

Starting dose for mtx

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lichen planopilaris methotrexate starting dose 10 mg 15 mg weekly clinical study

For active confirmed LPP, a defensible starting regimen is:
  • Methotrexate 10-15 mg once weekly PO or SC.
  • In a young, otherwise healthy adult with clearly active/progressive disease and normal baseline screening, 15 mg once weekly is commonly used.
  • If you prefer a cautious escalation, start 10 mg once weekly, then increase to 15 mg once weekly after 2-4 weeks if tolerated and activity persists.
  • Never daily.
LPP-specific data include an RCT using 15 mg/week for 6 months, while a retrospective LPP series used an initial 10-15 mg/week with gradual tapering. Published broader lichen-planus series report 15-20 mg/week. The LPP RCT abstract and the LPP MTX series support that range.
Typical co-prescribing/monitoring:
  • Folic acid, per local protocol, commonly 5 mg weekly on a non-MTX day or 1 mg daily except MTX day
  • Baseline CBC, LFTs including albumin, creatinine/eGFR, hepatitis B/C screening, and infection/TB risk assessment as appropriate
  • CBC, LFTs, creatinine/eGFR every 1-2 weeks after initiation or dose escalation, then every 2-3 months when stable, per SPS monitoring guidance
Given the possibility of scalp infection or another cicatricial alopecia, I would document activity with trichoscopy and exclude tinea/folliculitis before immunosuppression.

Can i start with 2.5 mg mtx

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methotrexate low dose dermatology 2.5 mg weekly starting dose monitoring

2.5 mg once weekly can be used as a cautious test/start dose, but it is generally subtherapeutic for active LPP and should not be the intended treatment dose.
For a healthy 23-year-old with normal baseline CBC, LFTs, and renal function, a reasonable escalation approach is:
  • 2.5 to 5 mg once weekly for the first dose only if you want to assess tolerance or reduce dosing-error risk
  • then 10 mg once weekly
  • escalate to 15 mg once weekly after 2-4 weeks if tolerated and disease remains active
For LPP, published regimens are generally 10-15 mg/week initially, with an RCT using 15 mg/week. The 15-20 mg/week range is also reported in lichen planus/LPP experience. - Fitzpatrick's Dermatology, systemic therapies section
A 2.5 mg/week dose may be appropriate longer term only in a very frail patient, major renal impairment, marked low body weight, or prior toxicity, but is unlikely to suppress a clearly inflammatory LPP relapse.
Use folate and safety monitoring as usual. Most importantly: MTX once weekly only, with the day explicitly written on the prescription.

Prp in scarring lpp

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"lichen planopilaris" AND "platelet-rich plasma"

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platelet rich plasma lichen planopilaris scarring alopecia randomized trial systematic review

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PMID: 38525908

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PMID: 41081974

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PMID: 37852211

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https://pmc.ncbi.nlm.nih.gov/articles/PMC13425247

PRP can be considered as an adjunct in LPP, including scarring LPP, but not as a substitute for controlling active lymphocytic inflammation.

Evidence

The best direct study is a small single-blind RCT of 24 LPP patients:
  • Both groups used clobetasol 0.05% nightly
  • PRP arm received 3 intradermal PRP sessions, one month apart
  • PRP plus clobetasol had lower LPPAI at months 2 and 6, better patient satisfaction, and no serious adverse effects. Behrangi et al., 2024 RCT, PMID 38525908
A 2025 systematic review of procedures for LPP/FFA/DLE found platelet-derived products had the most consistent procedural evidence for reducing activity scores and symptoms, but emphasized that studies are few, protocols vary, and procedures remain adjuncts to medical therapy. Systematic review, PMID 41081974

Practical approach

For a patient with active LPP:
  • First document activity: LPPAI, symptoms, perifollicular erythema/scale/casts, pull test, serial standardized photos and trichoscopy.
  • Treat inflammation with your chosen medical regimen.
  • Add PRP if active symptoms/signs persist, if systemic treatment is unsuitable, or as an adjunct where there are still viable follicles.
A pragmatic protocol based on the RCT is:
  • 3 monthly sessions of intradermal autologous PRP, while continuing topical anti-inflammatory therapy.
  • Review at months 3 and 6 using symptoms plus trichoscopy/photographs, not density alone.

Set expectations

  • PRP may reduce burning, itch, perifollicular erythema/scale, and shedding.
  • It may improve thickness/density only where follicles remain viable.
  • It will not regrow hair in smooth shiny scarred scalp with absent follicular ostia.
  • I would avoid calling it monotherapy for progressing LPP, especially in someone previously needing prednisolone/methotrexate.
The recent EADV LPP position statement describes PRP as potentially improving signs, symptoms, and hair thickness with few adverse effects, while the overall LPP evidence base remains limited. EADV position statement
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