Comparison of clinical and serological differences among juvenile-, adult-, and late-onset systemic lupus erythematosus in Korean patients

Choi, Jong-il; Park, D J; Kang, Ji-Hyoun; Yim, Yi-Rang; Lee, K E; Lee, J W; Wen, Lihui; Kim, Tae‐Jong; Park, Y W; Lee, J K; Lee, S S

doi:10.1177/0961203315591024

Cited by 66 publications

(76 citation statements)

References 39 publications

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“…Recently, a study showed that ANA was present in 99.8% of 552 patients with SLE from South China; 81.3% of these subjects also displayed anti‐dsDNA antibodies . Interestingly, a study from Korea showed that anti‐dsDNA was found more frequently in juvenile SLE patients under 18 years old and less frequently in SLE patients over 50 years old ( P < 0.05) . However, the differential diagnosis between OLP and LE is difficult because they have similar oral manifestations .…”

Section: Discussionmentioning

confidence: 99%

Correlation of serum ANA and direct immunofluorescence studies in elderly Thai patients with red and white oral lesions

Thongprasom

Prapinjumrune

Kanjanabuch

et al. 2016

J Oral Pathology Medicine

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Section: Discussionmentioning

confidence: 99%

Correlation of serum ANA and direct immunofluorescence studies in elderly Thai patients with red and white oral lesions

Thongprasom

Prapinjumrune

Kanjanabuch

et al. 2016

J Oral Pathology Medicine

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“…Sicca syndrome, 4 pericarditis, and lung involvement are more common as initial manifestations of LO-SLE. Choi et al 5 reported that decreased complement levels are more common in juvenile SLE. Webb et al 6 reported that doublestranded deoxyribonucleic acid antibody results can be heterogeneous.…”

Section: Discussionmentioning

confidence: 99%

Coexistence of Late-Onset Systemic Lupus Erythematosus With Focal Segmental Glomerulosclerosis and Lichen Planus: A Case Report

Sargın

Gürer

2017

Arch Rheumatol

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Late-onset systemic lupus erythematosus (LO-SLE) is defined when SLE develops after the age of 50 years and occurs in 3 to 18% of SLE patients. This late onset age has a strong modifying effect on the clinical presentation, disease course, response to treatment, and prognosis of SLE. LO-SLE often has delayed diagnosis and less common occurrence of severe manifestations. Arnaud et al. 1 suggests that pulmonary involvement and serositis are more frequent in LO-SLE, whereas malar rash, photosensitivity, arthritis, and nephropathy occur less commonly.In this article, we report a male patient presenting with lichen planus (LP) and focal segmental glomerulosclerosis (FSGS) who was subsequently diagnosed with LO-SLE. Our literature scan did not reveal any report on FSGS and LP as an initial manifestation in LO-SLE. CASE REPORTA 57-year-old male patient presented with complaints of pain in both hands and skin lesions in the left ankle for the last one year (Figure 1). He described symmetric joint pain and morning stiffness for longer than one hour. He had a two-year history of arthralgia and of using topical steroid and nonsteroidal anti-inflammatory drugs. He did not have any history of cutaneous lesions, oral or nasal ulcers, alopecia, pleural effusion, neuropathy, psychosis, seizures or myelitis. He did not have previous laboratory analyses. He had no history of smoking or alcohol consumption, or hypertension. His general condition was moderate, oriented, and cooperated. His blood pressure was 160/80 mmHg, and heart rate and temperature were normal. Locomotor system ABSTRACT Lichen planus and lupus nephritis with late-onset systemic lupus erythematosus (LO-SLE) may occur concomitantly. However, coexistence of LO-SLE with focal segmental glomerulosclerosis and lichen planus has not been defined. In this article, we report a 57-year-old male patient presenting with lichen planus and focal segmental glomerulosclerosis who was subsequently diagnosed with LO-SLE. To the best of our knowledge, this is the first case of LO-SLE presenting with lichen planus and focal segmental glomerulosclerosis.

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“…This study was prospective case-control study carried out in the period from August 2016 to August 2017 after approval from the research ethical committee of the faculty of Medicine of Tanta University and informed written or verbal consents from parents of included patients on 50 Lupus patients with ages ranged from 10-18 years who were selected from outpatient clinic and inpatient wards of Pediatric Nephrology Unit of Pediatric Department of Tanta University Hospital who fulfilled the revised criteria of American College of Rheumatology (ACR) for diagnosis of SLE [8,9]. They were subdivided into 2 groups, group 1 included 50 known cases of SLE during renal disease activity (Active lupus nephritis) and group 2 included 30 known cases of SLE without activity (inactive SLE).…”

Section: Methodsmentioning

confidence: 99%

Sleep Architecture in Pediatric patients with Lupus Nephropathy

El-Gamasy¹

2017

Ped Health Res

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Comparison of clinical and serological differences among juvenile-, adult-, and late-onset systemic lupus erythematosus in Korean patients

Cited by 66 publications

References 39 publications

Correlation of serum ANA and direct immunofluorescence studies in elderly Thai patients with red and white oral lesions

Correlation of serum ANA and direct immunofluorescence studies in elderly Thai patients with red and white oral lesions

Coexistence of Late-Onset Systemic Lupus Erythematosus With Focal Segmental Glomerulosclerosis and Lichen Planus: A Case Report

Sleep Architecture in Pediatric patients with Lupus Nephropathy

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