Clinicopathological Features of Lupus Erythematosus Panniculitis (LEP): A Retrospective Analysis of 54 Cases

ABSTRACT Background Lupus Erythematosus Panniculitis (LEP) is a rare subtype of Cutaneous Lupus Erythematosus. It is a challenging disease to diagnose and treat due to limited understanding of its clinical and histopathological characteristics. Methods We conducted a retrospective review of 54 biopsy‐proven LEP cases evaluated at a dermatology referral center from 2016 to 2022. Demographic, clinical, laboratory, and treatment data were extracted from medical records, and histopathologic features were reassessed when slides required further characterization. Direct immunofluorescence and serologic results were recorded when available. Statistical analyses were performed using SPSS (v26), with significance defined as p < 0.05. Results Fifty‐four patients with LEP (female‐to‐male ratio 5:1; mean age 38.8 ± 14.7 years) were included. Coexistent systemic lupus erythematosus (SLE) was present in 24.1% of cases. Delayed diagnosis was significantly associated with lipoatrophy ( p < 0.001). Histopathologic findings most commonly included lymphocytic vasculitis (72.2%), histologic features of discoid lupus erythematosus (68.5%), and lobular panniculitis (63%). ANA, anti‐double‐stranded DNA, and direct immunofluorescence were positive in 24.1%, 16.6%, and 72.2% of patients, respectively. Overall, 85.2% of patients improved clinically. Hydroxychloroquine combined with corticosteroids and mycophenolate mofetil was associated with the highest improvement rates, whereas intralesional corticosteroid therapy appeared least effective, although differences were not statistically significant. Conclusion It is essential to evaluate the clinical and histopathologic features of patients accurately before diagnosis. Delay in diagnosis may be more common in patients without associated SLE or DLE, although these associations were not statistically significant in our cohort. Hydroxychloroquine‐based combination therapy, particularly with corticosteroids and mycophenolate mofetil, was associated with favorable clinical outcomes, although prospective studies are needed to establish optimal treatment strategies.

Authors

Institutions

Publication Details

Journal
Health Science Reports
Published
2026-07-25
DOI
https://doi.org/10.1002/hsr2.72871
Primary Topic
Systemic Lupus Erythematosus Research
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Clinicopathological Features of Lupus Erythematosus Panniculitis (LEP): A Retrospective Analysis of 54 Cases

Maryam Ghiasi, Kambiz Kamyab, Alireza Abdshah, Maryam Nasimi et al.
Health Science Reports
Systemic Lupus Erythematosus Research
article

Clinicopathological Features of Lupus Erythematosus Panniculitis (LEP): A Retrospective Analysis of 54 Cases

Maryam Ghiasi, Kambiz Kamyab, Alireza Abdshah, Maryam Nasimi, Sahar Montazeri, Hanie Babaie, Fatemeh Saberi, Narjes Ramezani
article en

Abstract

ABSTRACT Background Lupus Erythematosus Panniculitis (LEP) is a rare subtype of Cutaneous Lupus Erythematosus. It is a challenging disease to diagnose and treat due to limited understanding of its clinical and histopathological characteristics. Methods We conducted a retrospective review of 54 biopsy‐proven LEP cases evaluated at a dermatology referral center from 2016 to 2022. Demographic, clinical, laboratory, and treatment data were extracted from medical records, and histopathologic features were reassessed when slides required further characterization. Direct immunofluorescence and serologic results were recorded when available. Statistical analyses were performed using SPSS (v26), with significance defined as p < 0.05. Results Fifty‐four patients with LEP (female‐to‐male ratio 5:1; mean age 38.8 ± 14.7 years) were included. Coexistent systemic lupus erythematosus (SLE) was present in 24.1% of cases. Delayed diagnosis was significantly associated with lipoatrophy ( p < 0.001). Histopathologic findings most commonly included lymphocytic vasculitis (72.2%), histologic features of discoid lupus erythematosus (68.5%), and lobular panniculitis (63%). ANA, anti‐double‐stranded DNA, and direct immunofluorescence were positive in 24.1%, 16.6%, and 72.2% of patients, respectively. Overall, 85.2% of patients improved clinically. Hydroxychloroquine combined with corticosteroids and mycophenolate mofetil was associated with the highest improvement rates, whereas intralesional corticosteroid therapy appeared least effective, although differences were not statistically significant. Conclusion It is essential to evaluate the clinical and histopathologic features of patients accurately before diagnosis. Delay in diagnosis may be more common in patients without associated SLE or DLE, although these associations were not statistically significant in our cohort. Hydroxychloroquine‐based combination therapy, particularly with corticosteroids and mycophenolate mofetil, was associated with favorable clinical outcomes, although prospective studies are needed to establish optimal treatment strategies.

Health Science ReportsVol. 9(8)
Razi Hospital (IR), Tehran University of Medical Sciences (IR)
Good health and well-being
Openalex Percentile: Top 7%
Systemic Lupus Erythematosus Research
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.