Evidence map›Paper›PMID 41625830›Full record

ArticleCureus2025

Omalizumab Therapy for Bullous Pemphigoid: A Case Report.

Adel Alsantali, Reema S AlZaidi, Bader Alharbi, Ahmed K Bakhsh, Anhar K Zahrani, Mohammed I Alturkistani

Abstract readCase Reports
In one paragraph

Article in Cureus, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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.

2 · The registry

The trial behind it

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.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Adel AlsantaliDermatology, King Fahad Armed Forces Hospital, Jeddah, SAU.
Reema S AlZaidiDermatology, King Fahad Armed Forces Hospital, Jeddah, SAU.
Bader AlharbiDermatology, King Fahad Armed Forces Hospital, Jeddah, SAU.
Ahmed K BakhshDermatology, King Fahad Armed Forces Hospital, Jeddah, SAU.
Anhar K ZahraniDermatology, King Fahad Armed Forces Hospital, Jeddah, SAU.
Mohammed I AlturkistaniCollege of Medicine, Umm Al-Qura University, Makkah, SAU.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Bullous pemphigoid (BP) is a chronic autoimmune blistering disease characterized by the presence of autoantibodies that target hemidesmosomal proteins, specifically BP180 and BP230. This immune response leads to the formation of subepidermal blisters and inflammation. The primary treatment for BP involves systemic corticosteroids; however, long-term use can result in significant adverse effects, and some patients may experience resistance to steroid therapy. We report the case of a 62-year-old male with multiple comorbidities who developed progressive, itchy blisters and extensive skin erosions affecting more than 50% of his body surface. Although he initially showed improvement with intravenous corticosteroids, new blister formation continued, and Staphylococcus aureus bacteremia prevented further use of immunosuppressive therapy. The patient was managed with targeted antibiotics, intravenous immunoglobulin (IVIG), and omalizumab. This treatment resulted in significant clinical improvement, the resolution of new blister formation, and a successful tapering of corticosteroids. Omalizumab has demonstrated promising efficacy in treating BP, especially in refractory cases. Given its favorable safety profile, further clinical trials are needed to determine its long-term role in the management of BP.

Indexed as

autoimmune blistering diseasebullous pemphigoidige-targeted therapyomalizumabsteroid resistance

Identifiers

PMID41625830
PMCPMC12854155

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.