Kristo Alberto Nababan
Universitas Sumatera Utara & Adam Malik Hospital

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Relationship between High Sensitivity C-Reactive Protein Levels and the Severity of Vulgaris Psoriasis William Halomoan Francisco Purba; Kristo Alberto Nababan; Deryne Anggia Paramita
Indonesian Journal of Global Health Research Vol. 8 No. 3 (2026): Indonesian Journal of Global Health Research
Publisher : GLOBAL HEALTH SCIENCE GROUP

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.37287/ijghr.v8i3.1105

Abstract

Psoriasis vulgaris is a chronic immune-mediated inflammatory skin disease increasingly recognized as a systemic inflammatory condition. High-sensitivity C-reactive protein (hs-CRP) is a sensitive marker of systemic inflammation, but its relationship with psoriasis severity remains inconsistent. This research evaluate the association between serum hs-CRP levels and disease severity in patients with psoriasis vulgaris. To evaluate the association between serum hs-CRP levels and disease severity in patients with psoriasis vulgaris. A cross-sectional analytical study was conducted involving 30 patients with psoriasis vulgaris and 30 control subjects at a tertiary hospital in Indonesia. Samples were obtained using non-probability sampling with a consecutive sampling technique, in which subjects who met the inclusion criteria were recruited sequentially until the minimum required sample size was achieved. Psoriasis severity was assessed using the Psoriasis Area and Severity Index (PASI). Serum hs-CRP levels were measured using enzyme-linked immunosorbent assay. Correlations between hs-CRP levels and PASI scores were analyzed using Spearman’s rank test. Most psoriasis patients had mild disease (56.7%). The mean serum hs-CRP level in the psoriasis group was 1.23 mg/L. No significant correlation was found between hs-CRP levels and PASI scores (r = 0.128, p = 0.499) or categorical disease severity. Although hs-CRP levels were higher in psoriasis patients than controls, the difference was not statistically significant. Serum hs-CRP levels were not associated with clinical severity of psoriasis vulgaris, suggesting that hs-CRP reflects systemic inflammation rather than cutaneous disease severity alone.
Combination Therapy with Corticosteroids and Mycophenolate Mofetil in the Management of Pemphigus Vulgaris: A Case Report Ella Finarsih; Kristo Alberto Nababan
Indonesian Journal of Global Health Research Vol. 8 No. 4 (2026): Indonesian Journal of Global Health Research
Publisher : GLOBAL HEALTH SCIENCE GROUP

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.37287/ijghr.v8i4.1584

Abstract

Pemphigus vulgaris (PV) is a rare, potentially life-threatening autoimmune blistering disease caused by IgG autoantibodies against desmoglein proteins, leading to acantholysis and intraepidermal blister formation. The incidence of PV ranges from 0.76 new cases per million population per year in Finland to approximately 3.5 new cases per million population per year in other regions. Early diagnosis and appropriate immunosuppressive therapy are crucial to prevent disease progression and complications. This study aims to report the clinical presentation, diagnostic approach, and therapeutic outcome of combination therapy using systemic corticosteroids and mycophenolate mofetil in a patient with pemphigus vulgaris. This is a descriptive case report of a 40-year-old female diagnosed with pemphigus vulgaris. Clinical evaluation, histopathological examination, and therapeutic response were documented and analyzed. A 40-year-old woman who presented with a one-week history of painful, generalized flaccid bullae and erosions involving the face, scalp, trunk, and extremities. Histopathological examination revealed suprabasal intraepidermal blistering with a characteristic row of tombstones appearance, confirming the diagnosis of pemphigus vulgaris.Initial treatment with systemic corticosteroids resulted in partial clinical improvement; however, new lesions continued to develop. The addition of mycophenolate mofetil as a steroid-sparing agent led to significant disease control, with cessation of new blister formation and gradual healing of existing lesions. The patient showed marked clinical improvement with good functional and vital prognosis, although long-term remission remains uncertain. This case highlights a severe and extensive presentation of pemphigus vulgaris and emphasizes the importance of clinicopathological correlation for accurate diagnosis. Early combination therapy with systemic corticosteroids and mycophenolate mofetil may be effective in controlling refractory disease and minimizing corticosteroid-related adverse effects.