Blaschkoid lichen planus occurring in childhood systemic lupus erythematosus

Sil, Abheek; Chakraborty, Sayantani; Panigrahi, Avik; Mondal, Satarupa

doi:10.1111/pde.14130

Cited by 5 publications

(2 citation statements)

References 4 publications

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“…Besides celiac disease, the literature reports the association of LP with other autoimmune disorders, such as lupus erythematosus, Sjögren syndrome, psoriasis, Chron disease, and vitiligo. [27][28][29][30][31][32][33][34][35][36] It remains unclear whether LP and these autoimmune disorders are etiologically related or patients with LP are more likely to develop other autoimmune diseases. 35 Celiac disease is one of the most common autoimmune diseases in individuals with OLP, 35 with a prevalence of 14%.…”

Section: Discussionmentioning

confidence: 99%

Oral Lichen Planus Associated With Lichen Planus Pigmentosus and Lichen Sclerosus in Monozygotic Twins

Marques¹,

Santos²,

Silva³

et al. 2020

The American Journal of Dermatopathology

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Lichen planus (LP) is a mucocutaneous immunemediated disease of unknown etiology. It is more prevalent in women and usually occurs between the third and sixth decades of life. Oral lesions may or may not be associated with skin and genital lesions. Although the role of genetic factors is still undetermined, reports of LP in more than one family member are not uncommon. However, the occurrence of LP in monozygotic twins is rare. We report a rare case of 42-year-old female monozygotic twins presenting oral LP. This report is even rarer because one of the patients had cutaneous lesions of an unusual variant of LP (LP pigmentosus) and the other had an uncommon association with lichen sclerosus. The etiology and pathogenesis of LP are still uncertain. However, despite being rare, its occurrence in family members and monozygotic twins suggests that genetic factors are involved in its development.

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Section: Discussionmentioning

confidence: 99%

Oral Lichen Planus Associated With Lichen Planus Pigmentosus and Lichen Sclerosus in Monozygotic Twins

Marques¹,

Santos²,

Silva³

et al. 2020

The American Journal of Dermatopathology

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“…As lesões bucais do LE e LP manifestam-se com características clínicas semelhantes e os achados histológicos de ambas as doenças se sobrepõem (Sil et al, 2020). O histopatológico da biópsia da lesão do Líquen Plano Oral (LPO), apresenta-se como uma degeneração da camada basal, cristas epiteliais em formas de dentes de serra com infiltrado linfocitário e corpos apoptóticos, denominados de corpúsculos de Civatte, que podem ser vistos no tecido conjuntivo (Ribeiro et al, 2010).…”

Section: Introductionunclassified

Síndrome de sobreposição de Lúpus Eritematoso Sistêmico e Líquen Plano Oral: relato de caso

Lira

Oliveira

Kotovicz

et al. 2022

RSD

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A Síndrome de Sobreposição (SS) associada ao Lúpus Eritematoso Sistêmico (LES) e Líquen Plano (LP), entidade rara, é caracterizada por sinais clínicos e imuno-histopatológicos sincrônicos de ambos. Relatamos o caso de uma paciente do sexo feminino, 39 anos, com diagnóstico de LES, apresentando lesões intraorais cujas hipóteses diagnósticas foram Líquen Plano Oral (LPO) e LES. Neste cenário, o presente estudo teve como objetivo descrever as patologias citadas, assim como expor as dificuldades do processo diagnóstico da síndrome de sobreposição em questão, explanando as etapas da doença e o tratamento realizado. O trabalho foi realizado através de um estudo de caso com objetivos descritivos e abordagem qualitativa utilizando-se de conhecimentos clínicos da dermatologia, estomatologia e reumatologia, com base em pesquisa bibliográfica e revisão de literatura integrativa em bases de dados digitais juntamente com a análise de exames complementares, histopatológicos e de imunofluoerescência. Na biópsia de lesões clinicamente ambíguas, como no caso das lesões orais da paciente, características histopatológicas de um ou ambos os processos podem ser encontrados simultaneamente ou oscilando em períodos diferentes, dificultando o diagnóstico e complicando o prognóstico e tratamento. Assim, foi observado que a imunofluorescência direta (IFD) tornou-se uma ferramenta essencial para auxiliar no diagnóstico dessa condição. Este caso reforça que a SS possui um diagnóstico desafiador e seu tratamento envolve vários profissionais para gerenciá-la.

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A Review of Linear Lichen Planus Case Reports

Rousseau,

Nelson,

Rashid

2024

The American Journal of Dermatopathology

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Lichen linear planus is a rare variant of lichen planus that appears as pruritic, polygonal, purple papules in a blaschkoid distribution. This review critically assesses all reported cases of linear lichen planus (LLP) for proposed etiology, clinical and histologic traits, treatment options, and recurrence. A PubMed search from inception through March 2023, followed by article screening and full-text review, identified 51 unique cases of LLP. Data from each case including the sex of the patient, anatomic distribution of lesions, biopsy results, proposed etiology, treatment, and recurrence were recorded. LLP did not show a significant gender or age predilection, most frequently presented unilaterally with pruritus, and involved numerous anatomic regions. Various triggers including metal implants, vaccinations, infections, malignancy, and pregnancy were identified. The most common histopathologic descriptions included band-like lymphocytic or lichenoid infiltrate, basal liquefactive, vacuolar degeneration, hypergranulosis, hyperkeratosis, civatte or colloid bodies, melanin incontinence, and orthokeratosis. Treatment options, duration of treatment, and recurrence rate of LLP lesions were variable. Although LLP is rare, dermatologists should be aware of this presentation and appropriate diagnostic and treatment options because swift diagnosis can reduce patient morbidity.

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Blaschkoid lichen planus occurring in childhood systemic lupus erythematosus

Cited by 5 publications

References 4 publications

Oral Lichen Planus Associated With Lichen Planus Pigmentosus and Lichen Sclerosus in Monozygotic Twins

Oral Lichen Planus Associated With Lichen Planus Pigmentosus and Lichen Sclerosus in Monozygotic Twins

Síndrome de sobreposição de Lúpus Eritematoso Sistêmico e Líquen Plano Oral: relato de caso

A Review of Linear Lichen Planus Case Reports

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