ArticleCureus2024
Morphea and Extragenital Lichen Sclerosus Et Atrophicus Overlap.
Article in Cureus, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
2 citing papers in PubMed.
- Extragenital Lichen Sclerosus: A Review of the Literature.Dermatology and therapy · 2026Review
- Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
3 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Lichen sclerosus et atrophicus (LSA) is a chronic inflammatory condition that affects mainly the genital regions but can occur extragenitally. Extragenital LSA occurs far less often than the genitally located variety and in most cases has been reported in females. A 36-year-old male engineer presented with chronic itchy lesions on the right forearm for more than a year's duration. On clinical examination, he had hypopigmented atrophic patches with scaling, alopecia, and follicular plugging. Dermoscopy revealed white structureless areas with telangiectasia, comedo-like openings, and peripheral pigment network. Histopathologically, these findings corroborated the presence of hyperkeratosis, epidermal atrophy, thickened collagen, and chronic inflammation. Overlapping LSA with morphea was under consideration since clinical, dermoscopic, and histopathological features were similar between the two conditions. The diagnostic challenge for both disorders resides in their locality in the form of a spectrum of localised sclerosing disorders. This case clearly highlights the importance of combining clinical, dermoscopic, and histopathological assessments for the proper differentiation of LSA from other sclerosing diseases and thus ensuring proper management and care. This is a report on a case that has a unique dermoscopic presentation and may mimic other disorders, necessitating careful diagnostic consideration.
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.