High-risk human papillomavirus-associated vulvar neoplasia among women living with human immunodeficiency virus in Zambia.

HIV Zambia human papillomavirus virus vulvar cancer vulvar neoplasia

Journal

African journal of laboratory medicine
ISSN: 2225-2002
Titre abrégé: Afr J Lab Med
Pays: South Africa
ID NLM: 101603205

Informations de publication

Date de publication:
2022
Historique:
received: 21 02 2021
accepted: 24 02 2022
entrez: 24 6 2022
pubmed: 25 6 2022
medline: 25 6 2022
Statut: epublish

Résumé

Globally, women living with HIV have a higher risk of vulvar neoplasia than HIV-negative women. Vulvar neoplasia among women living with HIV has not previously been characterised in Zambia. This study determined the clinical and pathologic features of vulvar neoplasia among women living with HIV at the University Teaching Hospital, Lusaka, Zambia. We conducted a cross-sectional study of vulvar lesions among 53 women living with HIV who presented with vulvar lesions between July 2017 and February 2018. The study assessed clinical and histological characteristics and prevalence of high-risk human papillomavirus (HRHPV). Twenty-one patients were diagnosed with vulvar squamous cell carcinoma (VSCC), 20 with usual vulvar intraepithelial neoplasm (uVIN), and the rest with either benign lesions or non-neoplastic lesions (NNL). Participants' mean age was 40 years. Patients with VSCC were significantly older than those with NNL (mean (s.d.): 43 (21) vs 33 (10), VSCC was significantly more common among women aged ≥ 40 years. HRHPV in VSCC and high-grade squamous intraepithelial lesions was high. Women with vulvar lesions, especially those aged > 40 years, should be evaluated for vulvar cancer. Young girls should be vaccinated to prevent vulvar cancer.

Sections du résumé

Background UNASSIGNED
Globally, women living with HIV have a higher risk of vulvar neoplasia than HIV-negative women. Vulvar neoplasia among women living with HIV has not previously been characterised in Zambia.
Objective UNASSIGNED
This study determined the clinical and pathologic features of vulvar neoplasia among women living with HIV at the University Teaching Hospital, Lusaka, Zambia.
Methods UNASSIGNED
We conducted a cross-sectional study of vulvar lesions among 53 women living with HIV who presented with vulvar lesions between July 2017 and February 2018. The study assessed clinical and histological characteristics and prevalence of high-risk human papillomavirus (HRHPV).
Results UNASSIGNED
Twenty-one patients were diagnosed with vulvar squamous cell carcinoma (VSCC), 20 with usual vulvar intraepithelial neoplasm (uVIN), and the rest with either benign lesions or non-neoplastic lesions (NNL). Participants' mean age was 40 years. Patients with VSCC were significantly older than those with NNL (mean (s.d.): 43 (21) vs 33 (10),
Conclusion UNASSIGNED
VSCC was significantly more common among women aged ≥ 40 years. HRHPV in VSCC and high-grade squamous intraepithelial lesions was high. Women with vulvar lesions, especially those aged > 40 years, should be evaluated for vulvar cancer. Young girls should be vaccinated to prevent vulvar cancer.

Identifiants

pubmed: 35747556
doi: 10.4102/ajlm.v11i1.1563
pii: AJLM-11-1563
pmc: PMC9210187
doi:

Types de publication

Journal Article

Langues

eng

Pagination

1563

Subventions

Organisme : FIC NIH HHS
ID : D43 TW010354
Pays : United States
Organisme : NCI NIH HHS
ID : U54 CA221204
Pays : United States

Informations de copyright

© 2022. The Authors.

Déclaration de conflit d'intérêts

The authors declare that they have no financial or personal relationships that may have inappropriately influenced them in writing this article.

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Auteurs

Fred Maate (F)

Department of Pathology and Microbiology, Adult and Emergency Hospital, University Teaching Hospitals, Lusaka, Zambia.
Department of Pathology and Microbiology, School of Medicine, University of Zambia, Lusaka, Zambia.

Peter Julius (P)

Department of Pathology and Microbiology, School of Medicine, University of Zambia, Lusaka, Zambia.

Stepfanie Siyumbwa (S)

Department of Pathology and Microbiology, Adult and Emergency Hospital, University Teaching Hospitals, Lusaka, Zambia.

Leeya Pinder (L)

Department of Obstetrics and Gynecology, University of Washington, Seattle, Washington, United States.

Trevor Kaile (T)

Department of Pathology and Microbiology, School of Medicine, University of Zambia, Lusaka, Zambia.

Mulindi Mwanahamuntu (M)

Department of Obstetrics and Gynaecology, Women and Newborn Hospital, University Teaching Hospitals, Lusaka, Zambia.

Groesbeck Parham (G)

Department of Obstetrics and Gynecology, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, United States.

Classifications MeSH