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Diagnostic utility of PRAME expression by immunohistochemistry in subungual and non-subungual acral melanocytic lesions.
Rothrock, Aimi T; Torres-Cabala, Carlos A; Milton, Denái R; Cho, Woo Cheal; Nagarajan, Priyadharsini; Vanderbeck, Kaitlin; Curry, Jonathan L; Ivan, Doina; Prieto, Victor G; Aung, Phyu P.
Afiliação
  • Rothrock AT; Department of Pathology, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
  • Torres-Cabala CA; Department of Pathology, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
  • Milton DR; Department of Biostatistics, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
  • Cho WC; Department of Pathology, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
  • Nagarajan P; Department of Pathology, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
  • Vanderbeck K; Department of Pathology, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
  • Curry JL; Department of Pathology, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
  • Ivan D; Department of Pathology, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
  • Prieto VG; Department of Pathology, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
  • Aung PP; Department of Pathology, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
J Cutan Pathol ; 49(10): 859-867, 2022 Oct.
Article em En | MEDLINE | ID: mdl-35794643
ABSTRACT

BACKGROUND:

The immunohistochemical (IHC) marker PReferentially expressed Antigen in MElanoma (PRAME) has shown promise in the diagnosis of melanocytic lesions. A few studies have investigated PRAME IHC expression in acral melanomas, but PRAME expression in subungual melanomas is largely unknown. We evaluated the utility of PRAME IHC expression in distinguishing subungual melanomas (SUM) and non-subungual acral melanomas (AM) from acral nevi (AN).

METHODS:

Twenty-two SUM, 20 AM, and 14 AN were identified. IHC studies were performed using an anti-PRAME antibody. The percentage of lesional cells with PRAME expression was recorded and categorized as follows 0%, 0; 1%-25%, 1+; 26%-50%, 2+; 51%-75%, 3+; and >75%, 4+. Patient demographics and other relevant clinicopathologic parameters were recorded.

RESULTS:

Diffuse (4+) PRAME IHC expression was identified in 55% (12/22) SUM and 70% (14/20) AM, respectively. Any PRAME expression (1+ to 4+) was identified in 73% (16/22) SUMs and 95% (19/20) AM, respectively. One of 14 (7%) AN exhibited PRAME expression; interestingly, the pattern of expression was diffuse.

CONCLUSIONS:

In our study, PRAME IHC expression was useful in identifying AM, including SUM. However, there are exceptions of PRAME-negative melanomas and PRAME-positive nevi.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias Cutâneas / Nevo de Células Epitelioides e Fusiformes / Melanoma / Doenças da Unha / Nevo Tipo de estudo: Diagnostic_studies / Prognostic_studies Limite: Humans Idioma: En Revista: J Cutan Pathol Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias Cutâneas / Nevo de Células Epitelioides e Fusiformes / Melanoma / Doenças da Unha / Nevo Tipo de estudo: Diagnostic_studies / Prognostic_studies Limite: Humans Idioma: En Revista: J Cutan Pathol Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Estados Unidos