Perilous polymers: a case of hydrophilic gel polymer embolism

Hydrophilic polymer embolism (HPE) is a rare complication of endovascular procedures caused by embolization of polymer coatings from vascular devices. We report a 72-year-old man with peripheral artery disease, diabetes, and chronic kidney disease who developed painful, nonhealing lower-extremity ulcers presenting shortly after vascular stenting. Initial biopsies and an extensive infectious and autoimmune workup were nondiagnostic, and the patient failed treatment for presumed pyoderma gangrenosum. Repeat biopsies later revealed amorphous blue material in dermal vessels, highlighted by Alcian blue staining, confirming HPE. Despite treatment with pentoxifylline and wound care, disease progression led to bilateral below-the-knee amputations. This case highlights the diagnostic challenge of HPE, which can present months after endovascular intervention and mimic other ulcerative disorders. Histologic findings are subtle, and early coordination with dermatopathology is key. Clinicians should maintain high suspicion for HPE in patients with unexplained ulcers and vascular procedure history, as early recognition may reduce morbidity.

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Publication Details

Journal
Baylor University Medical Center Proceedings
Published
2025-09-29
DOI
https://doi.org/10.1080/08998280.2025.2563487
Primary Topic
Geochemistry and Geologic Mapping
Type
article
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article

Perilous polymers: a case of hydrophilic gel polymer embolism

Baylor University Medical Center Proceedings
Geochemistry and Geologic Mapping
article

Perilous polymers: a case of hydrophilic gel polymer embolism

article en

Abstract

Hydrophilic polymer embolism (HPE) is a rare complication of endovascular procedures caused by embolization of polymer coatings from vascular devices. We report a 72-year-old man with peripheral artery disease, diabetes, and chronic kidney disease who developed painful, nonhealing lower-extremity ulcers presenting shortly after vascular stenting. Initial biopsies and an extensive infectious and autoimmune workup were nondiagnostic, and the patient failed treatment for presumed pyoderma gangrenosum. Repeat biopsies later revealed amorphous blue material in dermal vessels, highlighted by Alcian blue staining, confirming HPE. Despite treatment with pentoxifylline and wound care, disease progression led to bilateral below-the-knee amputations. This case highlights the diagnostic challenge of HPE, which can present months after endovascular intervention and mimic other ulcerative disorders. Histologic findings are subtle, and early coordination with dermatopathology is key. Clinicians should maintain high suspicion for HPE in patients with unexplained ulcers and vascular procedure history, as early recognition may reduce morbidity.

Baylor University Medical Center ProceedingsVol. 39(2)
Baylor College of Medicine (US), Kio University (JP), Baylor Medical Center at Garland (US)
Openalex Percentile: Top 25%
Geochemistry and Geologic Mapping
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Perilous polymers: a case of hydrophilic gel polymer embolism · Baylor University Medical Center Proceedings (2025) | TGRS Research Map | TGRS