Evidence map›Paper›PMID 42180729›Full record

ArticleFrontiers in medicine2026

Case Report: Successful treatment of dystrophic epidermolysis bullosa pruriginosa with upadacitinib in a patient with

Hao Li, Yu Zhang, Xuewen Lin, Tianmeng Yan, Xiaoyan Wu, Zhenying Zhang

Abstract readCase Reports
In one paragraph

Article in Frontiers in medicine, 2026. 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.

Hao LiDepartment of Dermatology, The University of Hong Kong-Shenzhen Hospital, Shenzhen, China.
Yu ZhangDepartment of Dermatology, The University of Hong Kong-Shenzhen Hospital, Shenzhen, China.
Xuewen LinDepartment of Dermatology, The University of Hong Kong-Shenzhen Hospital, Shenzhen, China.
Tianmeng YanDepartment of Dermatology, The University of Hong Kong-Shenzhen Hospital, Shenzhen, China.
Xiaoyan WuDepartment of Dermatology, The University of Hong Kong-Shenzhen Hospital, Shenzhen, China.
Zhenying ZhangDepartment of Dermatology, The University of Hong Kong-Shenzhen Hospital, Shenzhen, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Dystrophic epidermolysis bullosa pruriginosa (DEB-Pr) is a rare subtype of dystrophic epidermolysis bullosa (DEB) characterized by intensely pruritic blisters, prurigo-like nodules, and scarring on the extensor aspects of the extremities. We present a 43-year-old female patient with a 30-year history of recurrent erythematous plaques, nodules, and blisters, which was accompanied by severe pruritus affecting the scalp, back, and extremities. Whole-exome sequencing identified a heterozygous likely pathogenic variant in

Indexed as

CARD14case reportCOL7A1dystrophic epidermolysis bullosa pruriginosaG6PDgenetic variantJAK inhibitorupadacitinib

Identifiers

PMID42180729
PMCPMC13194394

What OpenQuestion holds

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Registered trials

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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.