PRAME and LEF1 in Combined Deep Penetrating Nevus and Combined Blue Nevus: Utility and Pitfalls.


Journal

The American Journal of dermatopathology
ISSN: 1533-0311
Titre abrégé: Am J Dermatopathol
Pays: United States
ID NLM: 7911005

Informations de publication

Date de publication:
01 08 2023
Historique:
pmc-release: 01 08 2024
medline: 19 7 2023
pubmed: 18 7 2023
entrez: 18 7 2023
Statut: ppublish

Résumé

Deep penetrating nevi (DPN), particularly those showing combined features, or combined deep penetrating nevi (CDPN), may show histopathological resemblance to blue nevus (BN) and melanoma. Preferentially Expressed Antigen in MElanoma (PRAME) is a marker that helps distinguish melanoma from benign melanocytic lesions. Lymphoid enhancer-binding factor 1 (LEF1) has been proposed to be used in conjunction with β-catenin for diagnosis of DPN. The immunohistochemical expression of PRAME and LEF1 was evaluated in 10 DPN (including 6 CDPN and 2 DPN-like proliferations with atypical features), 16 BN (including combined and cellular BN), and 2 melanomas with features of DPN or BN. PRAME was negative in most DPN (n = 10/10, n = 9/10, one case with discrepancy between readers) and all BN (n = 16/16), while the 2 melanomas included were positive (n = 2/2). All DPN were positive for LEF1 (n = 9/9) while only a subset of BN were positive (n = 6/16, P = 0.0028; n = 5/16, P = 0.001, per both readers). LEF1 seemed to be easier to interpret than β-catenin because of its nuclear pattern of expression. The expression of LEF1 in the regular nevus component of combined BN presents a potential pitfall in practice because it may lead to misinterpretation of LEF1 as positive in the BN component of the lesion. However, a subset (approximately one-third) of combined BN seemed to show true LEF1 expression. Taking into account pitfalls in interpretation, the combinatorial panel of PRAME and LEF1, in addition to conventional histopathological features, may be useful to distinguish CDPN from combined BN and other benign and malignant mimics.

Identifiants

pubmed: 37462205
doi: 10.1097/DAD.0000000000002488
pii: 00000372-202308000-00005
pmc: PMC10534018
mid: NIHMS1907293
doi:

Substances chimiques

beta Catenin 0
Lymphoid Enhancer-Binding Factor 1 0
Transcription Factors 0
PRAME protein, human 0
Antigens, Neoplasm 0
LEF1 protein, human 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

549-556

Subventions

Organisme : NCI NIH HHS
ID : P30 CA016672
Pays : United States

Informations de copyright

Copyright © 2023 Wolters Kluwer Health, Inc. All rights reserved.

Déclaration de conflit d'intérêts

The authors declare no conflicts of interest.

Références

J Cutan Pathol. 2020 Dec;47(12):1150-1154
pubmed: 32526042
Am J Surg Pathol. 1989 Jan;13(1):39-44
pubmed: 2909196
Am J Surg Pathol. 2020 Oct;44(10):1413-1418
pubmed: 32520758
Mod Pathol. 2013 Oct;26(10):1320-8
pubmed: 23599145
J Cutan Pathol. 2021 Apr;48(4):597-600
pubmed: 33094849
Cell. 2005 Sep 23;122(6):835-47
pubmed: 16179254
Eur J Dermatol. 2014 Sep-Oct;24(5):594-602
pubmed: 25118781
Immunity. 1997 Feb;6(2):199-208
pubmed: 9047241
Nat Commun. 2017 Sep 21;8(1):644
pubmed: 28935960
Am J Surg Pathol. 2022 Nov 1;46(11):1467-1476
pubmed: 35973038
Mod Pathol. 2020 Oct;33(10):2067-2074
pubmed: 32404956
Clin Sarcoma Res. 2017 Jun 15;7:11
pubmed: 28630682
J Thorac Oncol. 2016 Dec;11(12):2208-2217
pubmed: 27544054
J Cutan Pathol. 2020 Dec;47(12):1123-1131
pubmed: 32700786
Histopathology. 2021 Sep;79(3):291-305
pubmed: 33772838
J Am Acad Dermatol. 1994 May;30(5 Pt 1):724-9
pubmed: 8176011
Pigment Cell Melanoma Res. 2022 Mar;35(2):229-237
pubmed: 34633770
Oncotarget. 2016 Jul 19;7(29):45352-45369
pubmed: 27322684
Mod Pathol. 2022 Aug;35(8):1110-1120
pubmed: 35184152
Am J Dermatopathol. 2022 Jun 1;44(6):404-410
pubmed: 34991102
Biology (Basel). 2022 Mar 17;11(3):
pubmed: 35336833
Int J Cancer. 2020 Apr 15;146(8):2229-2242
pubmed: 31463973
Am J Cancer Res. 2017 Jun 01;7(6):1389-1406
pubmed: 28670499
Arch Pathol Lab Med. 2011 Mar;135(3):321-6
pubmed: 21366455
Histopathology. 1991 Mar;18(3):243-7
pubmed: 2045075
Virchows Arch. 2019 May;474(5):539-550
pubmed: 30756182
Appl Immunohistochem Mol Morphol. 2018 Oct;26(9):648-653
pubmed: 28027119
Am J Surg Pathol. 2018 Nov;42(11):1456-1465
pubmed: 30045064
Am J Dermatopathol. 2018 Jul;40(7):469-478
pubmed: 29923908
Proc Natl Acad Sci U S A. 2016 Mar 29;113(13):3545-50
pubmed: 26969725
Cancers (Basel). 2021 Jun 19;13(12):
pubmed: 34205480
Cancer Epidemiol Biomarkers Prev. 2017 Jul;26(7):1107-1113
pubmed: 28377414

Auteurs

Kaitlin Vanderbeck (K)

Departments of Department of Pathology.

Aimi T Rothrock (AT)

Departments of Department of Pathology.

Woo Cheal Cho (WC)

Departments of Department of Pathology.

Priyadharsini Nagarajan (P)

Departments of Department of Pathology.

Phyu P Aung (PP)

Departments of Department of Pathology.

Courtney Hudgens (C)

Translational Molecular Pathology.

Roland L Bassett (RL)

Biostatistics, and.

Doina Ivan (D)

Departments of Department of Pathology.

Victor G Prieto (VG)

Departments of Department of Pathology.
Dermatology, The University of Texas, MD Anderson Cancer Center, Houston, TX.

Jonathan L Curry (JL)

Departments of Department of Pathology.
Translational Molecular Pathology.

Carlos A Torres-Cabala (CA)

Departments of Department of Pathology.
Dermatology, The University of Texas, MD Anderson Cancer Center, Houston, TX.

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Classifications MeSH