Evidence map›Paper›PMID 41737082›Full record

ArticleCureus2026

Elephantiasis Nostra Verrucosa Complicated by Cellulitis and Hemorrhagic Bullae: A Rare and Severe Clinical Presentation.

Amna Nadeem, Iqra Choudhry

Abstract readCase Reports
In one paragraph

Article in Cureus, 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

2 authors.

Amna NadeemInternal Medicine, St. George's University School of Medicine, Saint George's, GRD.
Iqra ChoudhryPodiatry, Humboldt Park Health, Chicago, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Elephantiasis nostras verrucosa (ENV) is a rare and debilitating manifestation of chronic nonfilarial lymphedema characterized by progressive dermal fibrosis, hyperkeratosis, and papillomatous skin changes. It arises from long-standing lymphatic obstruction and is most commonly associated with risk factors such as obesity, venous insufficiency, recurrent soft tissue infections, and conditions impairing lymphatic drainage. The true prevalence of ENV is poorly defined due to its rarity, though limited institutional data suggest it is uncommon even among high-risk populations. While ENV typically presents as slowly progressive limb enlargement with characteristic skin changes, atypical features may indicate advanced disease or superimposed infection. We report the case of a 48-year-old male with chronic lower-extremity lymphedema complicated by recurrent cellulitis who developed progressive cutaneous changes consistent with evolving ENV and was further complicated by the appearance of hemorrhagic bullae. This uncommon finding raised concern for severe infection and potential vascular compromise. Management focused on treating acute bacterial cellulitis while addressing the underlying lymphatic dysfunction through aggressive conservative measures. This case highlights the importance of early recognition of atypical skin findings in chronic lymphedema and reinforces the central role of lymphedema control in preventing disease progression and serious complications.

Indexed as

case reportcellulitischronic lymphedemaelephantiasis nostras verrucosahemorrhagic bullae

Identifiers

PMID41737082
PMCPMC12926688

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.