Evidence map›Paper›PMID 42200754›Full record

ArticleThe American Journal of dermatopathology2026

Diagnostic and Prognostic Values of PRAME Immunohistochemistry in Acral Lentiginous Melanoma.

Korn Triyangkulsri, Namthong Wittayabusarakam, Supachak Smitthisakda, Nawara Sakpuwadol, Kunlawat Thadanipon, Bantita Phruttinarakorn, Suthinee Rutnin

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Article in The American Journal of dermatopathology, 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

7 authors.

Korn TriyangkulsriDivision of Dermatology, Department of Medicine, Faculty of Medicine, Ramathibodi Hospital, Mahidol University, Bangkok, Thailand.ORCID 0000-0001-8552-9277
Namthong WittayabusarakamDivision of Dermatology, Department of Medicine, Faculty of Medicine, Ramathibodi Hospital, Mahidol University, Bangkok, Thailand.
Supachak SmitthisakdaDivision of Dermatology, Department of Medicine, Faculty of Medicine, Ramathibodi Hospital, Mahidol University, Bangkok, Thailand.
Nawara SakpuwadolDivision of Dermatology, Department of Medicine, Faculty of Medicine, Ramathibodi Hospital, Mahidol University, Bangkok, Thailand.
Kunlawat ThadaniponDivision of Dermatology, Department of Medicine, Faculty of Medicine, Ramathibodi Hospital, Mahidol University, Bangkok, Thailand.
Bantita PhruttinarakornDepartment of Pathology, Faculty of Medicine, Ramathibodi Hospital, Mahidol University, Bangkok, Thailand .
Suthinee RutninDivision of Dermatology, Department of Medicine, Faculty of Medicine, Ramathibodi Hospital, Mahidol University, Bangkok, Thailand.ORCID 0000-0001-8268-8790

Funding

Faculty of Medicine Ramathibodi Hospital, Mahidol University, Bangkok, Thailand
6 · The paper itself

Abstract

backgroundPReferentially Expressed Antigen in MElanoma (PRAME) was introduced as an ancillary tool for confirming the diagnosis of cutaneous melanoma, including the acral lentiginous melanoma (ALM). However, its standardized cut-off values and prognostic performance remain inconclusive. This study assessed the diagnostic performance of PRAME immunohistochemistry (IHC) in ALM across different thresholds and explored its prognostic associations.

methodsThis retrospective cohort study reviewed 90 acral melanocytic lesions, including 60 cases of acral benign nevi and 30 cases of primary ALM. PRAME immunohistochemistry was performed on the biopsy specimens. Sensitivity and specificity were calculated at varying cut-offs. The optimal threshold was applied to link PRAME expression with the outcome and features of ALM.

resultsA PRAME staining threshold of 50% (score ≥3) provided the optimum cut-off for differentiating ALM, with a high specificity of 98.3% and sensitivity of 53.3%. Positive PRAME was significantly associated with higher TNM stages (ordinal odds ratio [95% confidence interval], 13.11 [2.55-67.27]) and higher rates of recurrence (hazard ratio, 6.62 [1.42-30.94]) but not with any unfavorable histopathological features or mortality.

conclusionPRAME can be used as an adjunctive diagnostic tool to differentiate malignant from benign acral melanocytic lesions. It may serve as a prognostic marker for poor ALM outcomes.

Indexed as

Antigens, NeoplasmBiomarkers, TumorMelanomaSkin NeoplasmsAdolescentAdultAgedAged, 80 and overCutaneous Malignant MelanomaFemaleHumansImmunohistochemistryMaleMiddle AgedPredictive Value of TestsPrognosisAntigens, NeoplasmBiomarkers, TumorPRAME protein, humanlentiginesmelanocytemelanonychianailnevus

Identifiers

PMID42200754
PMCPMC13489763

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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.