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Can J Ophthalmol. 2012 Aug;47(4):333-8. doi: 10.1016/j.jcjo.2012.04.013. Epub 2012 Jun 27.

Eyelash alopecia areata: case series and literature review.

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  • 1Eye Center, University of California, Davis School of Medicine, Davis, Calif., USA.

Abstract

OBJECTIVES:

To characterize the clinical presentations, features, and outcomes of eyelash alopecia areata.

DESIGN:

Retrospective chart review of patients evaluated for eyelash loss and found to have eyelash alopecia areata. A 3-year follow-up was required.

PARTICIPANTS:

The study involved 15 patients.

METHODS:

Patients who presented at a tertiary care eye clinic for evaluation of eyelash loss and were found to have eyelash alopecia areata were reviewed. Demographic considerations were categorized; they included age at presentation, areas of other hair loss, other relevant history, and treatment responses.

RESULTS:

Patients were young (mean age 18 years) and had a large female predominance (female-to-male ratio, 14:1). Concurrent scalp and brow involvement, either in isolation (20% and 13%, respectively) or together (13%), were seen in half of the patients (46%). Upper eyelid involvement was more common and severe than lower eyelid involvement, and 40% of patients experienced complete regrowth of lashes, with a mean time to regrowth of 28 months (range, 6 to 60 months). Of these, 13% experienced partial regrowth. Younger age at presentation was associated with regrowth, whereas presence or absence of other involved sites, personal or family histories of atopy, family history of alopecia, other autoimmune diseases, or the use of topical steroids did not appear to affect prognosis.

CONCLUSIONS:

Eyelash alopecia areata is a unique entity, although it remains potentially underdiagnosed. The key differential diagnosis is trichotillomania, which is commonly associated with obsessive-compulsive disorders. The presence of exclamation-mark hairs in alopecia areata plays an important role in differentiating the 2 diagnoses.

Copyright © 2012 Canadian Ophthalmological Society. Published by Elsevier Inc. All rights reserved.

PMID:
22883840
[PubMed - indexed for MEDLINE]
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