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  • Presentation

Trichoscopy in Alopecia: Distinguishing Scarring and Non-Scarring Hair Loss with Case-Based Findings

Description

The talk reviewed how trichoscopy helps distinguish normal scalp from scarring and non-scarring alopecia and identify specific disease patterns. Normal pigmented scalp shows an intact honeycomb pigment network, translucent follicular openings, and regularly distributed white dots. In non-scarring alopecia, the follicular openings and pigment network are preserved, while scarring alopecia shows loss of follicular ostia, disruption of the network, white patches, stellate macules, and irregular white dots. Case examples illustrated alopecia areata with broken hairs, black dots, exclamation point hairs, yellow dots, circle/pigtail hairs, short vellus hairs, and upright regrowth, with trichoscopy also helping gauge disease activity and recovery. Tinea capitis was distinguished by atypical hairs such as comma, corkscrew, zigzag, and Morse code hairs, plus white sheets; trichoscopy can even guide empiric treatment choices while cultures are pending. Discoid lupus showed scarring changes with keratotic plugs, erythema, blue-gray dots, and branching vessels. Traction alopecia featured hair casts and the flambeau sign, indicating chronic traction and risk of scarring. Psoriasis was contrasted with seborrheic dermatitis by silvery-white scale, red dots, twisted loops, and nail pitting, while CCCA and LPP showed scarring features including pigment loss and blue-gray halos. The speaker concluded that dermatoscopy is invaluable for diagnosis, management, and patient education, and noted emerging UV-induced fluorescence trichoscopy for identifying active follicles and infections.

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Conclusions

  • Trichoscopy is a valuable first-line tool for diagnosing hair loss because it can distinguish normal scalp anatomy from scarring and non-scarring alopecias.
  • Preserved follicular openings and an intact honeycomb pigment network favor non-scarring alopecia, whereas loss of follicular ostia, white patches, and asterisk-like macules indicate scarring alopecia.
  • Alopecia areata is suggested by black dots, broken hairs, exclamation point hairs, yellow dots, and regrowing pigtail or circle hairs.
  • The pattern of trichoscopic findings in alopecia areata can help estimate disease activity, with broken hairs and exclamation point hairs indicating active disease and pigtail or vellus regrowth signaling recovery.
  • Tinea capitis can be recognized by atypical hair-shaft shapes such as comma, corkscrew, zigzag, and Morse code hairs, often with scale or white sheath.
  • Trichoscopy can guide empiric treatment choice in tinea capitis before cultures return, with Trichophyton features favoring terbinafine and Microsporum features favoring griseofulvin.
  • Discoid lupus erythematosus presents trichoscopically with loss of the honeycomb pattern, keratotic plugs, follicular red dots, branching vessels, and blue-gray dots.
  • Traction alopecia shows early signs such as hair casts and preserved vellus hairs, while chronic traction can progress to scarring and be marked by the flambeau sign.
  • Frontal fibrosing alopecia and CCCA are scarring alopecias that can be distinguished from androgenetic alopecia by loss of vellus hairs, peripollicular scale, and follicular fibrosis patterns.
  • Psoriasis of the scalp is suggested by white or silvery scale, erythema, twisted red loop vessels, and red dots, while seborrheic dermatitis more often shows yellow waxy scale and lacks red dots.
  • Androgenetic alopecia is characterized by hair miniaturization, reduced shaft thickness, increased diameter variability, and fewer hairs per follicular unit.
  • UV-induced fluorescence trichoscopy appears to improve visualization of active follicular openings and may help in both diagnosis and monitoring of alopecia and tinea capitis.
  • Showing trichoscopy images to patients can improve understanding, reinforce counseling, and support adherence to hairstyle or treatment recommendations.
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