Evidence map›Paper›PMID 39881923›Full record

ArticleCureus2024

A Case of Purpuric Papulopustular Eruption on the Extremities Developed During Erlotinib and Ramucirumab Combination Treatment, Resulting in Complete Regression Without Oral Prednisone or Discontinuing Chemotherapy.

Yoshihito Mima, Tsutomu Ohtsuka, Akihiro Tsujita, Yoshimasa Nakazato, Yuta Norimatsu

Abstract readCase Reports
In one paragraph

Article in Cureus, 2024. 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

5 authors.

Yoshihito MimaDepartment of Dermatology, Tokyo Metropolitan Police Hospital, Tokyo, JPN.
Tsutomu OhtsukaDepartment of Dermatology, International University of Health and Welfare Hospital, Tochigi, JPN.
Akihiro TsujitaDepartment of Respiratory Medicine, International University of Health and Welfare Hospital, Tochigi, JPN.
Yoshimasa NakazatoDepartment of Diagnostic Pathology, International University of Health and Welfare Hospital, Tochigi, JPN.
Yuta NorimatsuDepartment of Dermatology, International University of Health and Welfare Narita Hospital, Narita, JPN.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A 53-year-old woman undergoing combination therapy with epidermal growth factor receptor (EGFR) and vascular endothelial growth factor receptor (VEGFR) inhibitors for advanced lung cancer with brain metastases developed pustules and punctate purpura on both lower extremities. Histopathological examination revealed neutrophilic infiltration around the hair follicles and erythrocyte extravasation in the perivascular regions near the hair roots, leading to a diagnosis of purpuric papulopustular eruptions. The rash improved with oral doxycycline (100 mg/day) and topical corticosteroids. This case demonstrates that extensive purpuric drug eruptions without symptoms of vasculitis can be effectively managed with oral antibiotics, without the need for chemotherapy discontinuation or systemic corticosteroids. EGFR inhibitors can induce purpuric papulopustular eruptions through follicular occlusion and damage to vascular endothelial cells via inflammatory cells. In our case, the treatment duration was longer than previously reported, suggesting that VEGFR inhibitors delay wound healing and endothelial cell repair, potentially contributing to the development of purpuric papulopustular eruptions. As combination therapy with EGFR and VEGFR inhibitors was only introduced in 2022, to the best of our knowledge, the present case is the first of purpuric papulopustular eruptions occurring during this treatment regimen.

Indexed as

chemotherapy discontinuationcombination treatmentcomplete regressiondrug eruptionerlotinibpurpuric papulopustular eruptionramucirumab

Identifiers

PMID39881923
PMCPMC11775495

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