ArticleCureus2024
Use of Intravenous Immunoglobulin in the Treatment of Pemphigoid Gestationis: A Case Report.
Article in Cureus, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
What it found
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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.
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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
1 citing paper in PubMed.
- An Unusual Case of Refractory Pemphigoid Gestationis with Neonatal Involvement: An Intricate Therapeutic Challenge.Indian dermatology online journal · 2026Article
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Authors and funding
3 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Gestational pemphigoid is a rare autoimmune skin condition specific to pregnancy and the postpartum period, with a variable course. There are currently no standardized guidelines referring to evidence-based therapeutic strategies. Intravenous immunoglobulin (IVIG) has recently emerged as a safe and effective steroid-sparing option as a second-line treatment for cases refractory to conventional steroid therapy and for managing relapses. We present the case of a 36-year-old primigravida patient diagnosed with gestational pemphigoid who initially had a difficult clinical course despite treatment with high-dose oral steroids. A first cycle of IVIG combined with steroids (with a gradual dose tapering regimen) was administered, showing initial clinical improvement. However, the patient experienced a relapse that required a new increase in steroid dose and interruption of pregnancy due to fetal growth restriction. Given persistent disease activity at the first outpatient follow-up, a combination of oral steroids with a gradual dose tapering regimen, along with a new cycle of IV immunoglobulin and azathioprine, was initiated, leading to complete resolution by the 19th week of outpatient follow-up. No adverse effects associated with IVIG were reported during the course of follow-up.
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Registered trials
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