Evidence map›Paper›PMID 41835772›Full record

ArticleCureus2026

Diagnostic Utility of PRAME and SOX10 Immunostaining for Vulvar Melanocytic Lesions.

Kridtin Jarutatsanangkoon, Phitsinee Purngpiputtrakul, Suchanan Hanamornroongruang, Vuthinun Achariyapota, Panitta Sitthinamsuwan

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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.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Kridtin JarutatsanangkoonPathology, Faculty of Medicine, Siriraj Hospital, Mahidol University, Bangkok, THA.
Phitsinee PurngpiputtrakulPathology, Faculty of Medicine, Siriraj Hospital, Mahidol University, Bangkok, THA.
Suchanan HanamornroongruangPathology, Faculty of Medicine, Siriraj Hospital, Mahidol University, Bangkok, THA.
Vuthinun AchariyapotaObstetrics and Gynecology, Faculty of Medicine, Siriraj Hospital, Mahidol University, Bangkok, THA.
Panitta SitthinamsuwanPathology, Faculty of Medicine, Siriraj Hospital, Mahidol University, Bangkok, THA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundVulvar melanoma (VM) is a rare type of malignant melanoma. Clinical presentations typically show mass or bleeding. Benign melanocytic lesions of the vulva include genital lentigines and genital melanocytic nevus. SOX10 is a marker commonly used in melanocytic lesions, and the preferentially expressed antigen in melanoma (PRAME) is a recent marker that shows high specificity for malignant melanoma.

objectivesThe study is to evaluate the histopathology and immunohistochemistry of SOX10 and PRAME in VM and benign vulvar melanocytic lesions (genital lentigine and genital melanocytic nevus). MATERIALS AND

methodsAll cases of VM and benign vulvar melanocytic lesions were recruited. Clinical and pathological data were reviewed. SOX10 and PRAME immunohistochemistry were performed and compared between VM and benign vulvar melanocytic lesions.

resultsOf the total nine cases with VM, 6 (66.7%) presented with mass, 2 (22.2%) had mass with bleeding, and one (11.1%) developed urinary discomfort. Histopathologically, mucosal lentiginous melanoma is the most common subtype. Thirteen cases with benign melanocytic lesions were found. In immunohistochemical studies, SOX10 showed positivity in all 9 (100%) VM and all 13 (100%) benign melanocytic lesions. PRAME showed positivity in 7 (77.8%) cases. All 13 (100%) benign melanocytic lesions show negative stains for PRAME. The sensitivity of SOX10 and PRAME in the diagnosis of VM was 100% and 88.9%, respectively. The specificity of SOX10 and PRAME in the diagnosis of VM was 0% and 100%, respectively.

conclusionsSOX10 and PRAME are nuclear staining markers that can be used for diagnostic purposes and as adjunct markers for the diagnosis of VM and benign melanocytic lesions. PRAME immunostaining shows high specificity for melanoma and melanoma in situ.

Indexed as

diagnosisgenital lentiginegenital melanocytic nevusimmunostainingmucosal lentiginous melanomapramepreferentially translated antigen in melanomasox10special site nevusvulvar melanoma

Identifiers

PMID41835772
PMCPMC12978960

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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.