Symptomatic Vulvar Primary Cutaneous Amyloidosis Associated With Low–Risk <scp>HPV</scp> : A Case Report

Primary localized cutaneous amyloidosis (PCLA) of the vulva is an infrequent diagnosis. Its clinical presentation may mimic neoplastic or inflammatory lesions and could even be associated with human papillomavirus (HPV) of low or high oncogenic risk, making accurate diagnosis and exclusion of systemic involvement essential. A 73-year-old woman presented with a flat, macular, solitary vulvar lesion. Histologic evaluation revealed amyloid deposits in the papillary dermis, confirmed by Congo red staining and apple-green birefringence. HPV genotyping identified type 40, a low-risk genotype, with no evidence of intraepithelial neoplasia. The diagnosis of systemic amyloidosis was ruled out by a multidisciplinary team evaluation. A complete local excision was performed. After 33 months of follow-up, the patient remains in remission. This case highlights the importance of including PCLA in the differential diagnosis of vulvar lesions and suggests a potential role of HPV as a possible trigger for vulvar localized amyloidogenesis.

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Publication Details

Journal
Clinical Case Reports
Published
2026-01-28
DOI
https://doi.org/10.1002/ccr3.71966
Primary Topic
Amyloidosis: Diagnosis, Treatment, Outcomes
Type
article
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article

Symptomatic Vulvar Primary Cutaneous Amyloidosis Associated With Low–Risk HPV : A Case Report

Jorge Hoegl, Daniel Marquez, Ysleyer Silva
Clinical Case Reports
Amyloidosis: Diagnosis, Treatment, Outcomes
article

Symptomatic Vulvar Primary Cutaneous Amyloidosis Associated With Low–Risk HPV : A Case Report

Jorge Hoegl, Daniel Marquez, Ysleyer Silva
article en

Abstract

Primary localized cutaneous amyloidosis (PCLA) of the vulva is an infrequent diagnosis. Its clinical presentation may mimic neoplastic or inflammatory lesions and could even be associated with human papillomavirus (HPV) of low or high oncogenic risk, making accurate diagnosis and exclusion of systemic involvement essential. A 73-year-old woman presented with a flat, macular, solitary vulvar lesion. Histologic evaluation revealed amyloid deposits in the papillary dermis, confirmed by Congo red staining and apple-green birefringence. HPV genotyping identified type 40, a low-risk genotype, with no evidence of intraepithelial neoplasia. The diagnosis of systemic amyloidosis was ruled out by a multidisciplinary team evaluation. A complete local excision was performed. After 33 months of follow-up, the patient remains in remission. This case highlights the importance of including PCLA in the differential diagnosis of vulvar lesions and suggests a potential role of HPV as a possible trigger for vulvar localized amyloidogenesis.

Clinical Case ReportsVol. 14(2)
Universidad Autónoma del Carmen (MX), Hospital Clínico Universitario de Caracas (VE), Petroleum of Venezuela (Venezuela) (VE), Universidad Central de Venezuela (VE)
Reduced inequalities, Gender equality
Openalex Percentile: Top 75%
Amyloidosis: Diagnosis, Treatment, Outcomes
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