Evidence map›Paper›PMID 40385924›Full record

ArticleCureus2025

Acute Hemorrhagic Edema of Infancy: A Rare Cause of Bilateral Ear Erythema.

Naima Rasul, Russell Delaney

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.

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0citing papers in PubMed
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1 · What the graph read from it

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.

2 · The registry

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3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

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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

2 authors.

Naima RasulMedical School, Edward Via College of Osteopathic Medicine, Blacksburg, USA.
Russell DelaneyPediatrics Department, Lewis Gale Medical Center, Salem, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Acute hemorrhagic edema of infancy (AHEI) is a rare cutaneous leukocytoclastic small-vessel vasculitis presenting with purpuric skin plaques on the face, ears, and extremities, frequently associated with fever and edema. Although the condition usually self-resolves over one to three weeks, it can be mistaken for more serious conditions, leading to unnecessary procedures and treatments. This case involves a nine-month-old infant who developed bilateral ear erythema and edema two days after a viral illness and was hospitalized for clinical suspicion of relapsing polychondritis. Within a couple of hours, the infant's erythema and edema progressed, with the appearance of small papules scattered across the right half of the face. Over five days, the patient developed purpuric lesions on the cheeks, chin, bilateral extremities, and trunk. During the hospitalization, the infant received empiric antibiotics, steroids, and antihistamines. Based on the acute edema, scattered purpuric lesions in the setting of a recent viral illness, and negative infectious workup, the infant was diagnosed with AHEI and subsequently managed with steroids to reduce the inflammation rapidly and antihistamines to reduce corticosteroid-induced gastric complications. The ear erythema, ear edema, and purpuric lesions showed resolution 10 days after initial presentation at the outpatient pediatric follow-up. However, while the infant was in good health overall at the outpatient dermatology follow-up approximately three weeks after hospitalization, he did have residual macular spots on the cheeks and bilateral lower extremities. The macular spots disappeared, and the infant had no cutaneous lesions two months after the initial presentation. The resolution of symptoms after oral steroids confirmed the clinical diagnosis of AHEI rather than relapsing polychondritis. This case serves to illustrate an unusual presentation of AHEI to aid in the future diagnosis of infantile rashes and to differentiate this benign diagnosis from other, life-threatening conditions. Early recognition of AHEI could prevent unnecessary treatments or procedures in the future.

Indexed as

acute edemaear painhenoch-schönlein purpuraleukocytoclastic vasculitispalpable purpuraperichondritisrash in childrenrelapsing polychondritis clinical picturesteroid-induced hiccupssteroid treatment

Identifiers

PMID40385924
PMCPMC12081774

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