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Diagnostic utility of SOX11 immunohistochemistry in differentiating cutaneous spread of mantle cell lymphoma from primary cutaneous B-cell lymphomas.
Hsi, Andy C; Hurley, M Yadira; Lee, Sena J; Rosman, Ilana S; Pang, Xiaofan; Gru, Alejandro; Schaffer, András.
Afiliação
  • Hsi AC; Department of Pathology and Immunology, Washington University School of Medicine, Saint Louis, MO, USA.
  • Hurley MY; Department of Dermatology, Saint Louis University School of Medicine, Saint Louis, MO, USA.
  • Lee SJ; Division of Dermatology, Washington University School of Medicine, Saint Louis, MO, USA.
  • Rosman IS; Department of Pathology and Immunology, Washington University School of Medicine, Saint Louis, MO, USA.
  • Pang X; Division of Dermatology, Washington University School of Medicine, Saint Louis, MO, USA.
  • Gru A; Department of Biology, Washington University in St. Louis, Saint Louis, MO, USA.
  • Schaffer A; Department of Pathology, The Ohio State University Medical Center, Columbus, OH, USA.
J Cutan Pathol ; 43(4): 354-61, 2016 Apr.
Article em En | MEDLINE | ID: mdl-26762898
ABSTRACT

BACKGROUND:

Mantle cell lymphoma (MCL) is associated with the worst prognosis among low-grade B-cell lymphomas. While cutaneous involvement by nodal or systemic MCL is uncommon, its differentiation from primary cutaneous B-cell lymphoma (CBCL) or cutaneous involvement by other extra-cutaneous BCL is challenging as neither histomorphology nor immunophenotype can be absolutely specific. We analyzed the diagnostic utility of SOX11 immunohistochemistry in differentiating secondary cutaneous MCL from other low-grade CBCL.

METHODS:

Immunohistochemical staining with anti-SOX11 antibody was performed on 8 cases of secondary cutaneous MCL, 16 secondary cutaneous CLL, 20 primary cutaneous MZL, 12 cutaneous FCL (6 primary, 6 secondary), 7 primary cutaneous DLBCL, leg type, 5 systemic DLBCL and 3 B-ALL. SOX11 and cyclin D1 staining were compared in secondary cutaneous MCL.

RESULTS:

Nuclear SOX11 staining was seen in seven of eight cases (88%) of secondary cutaneous MCL, including a case with minimal cyclin D1 expression. All other CBCL lacked detectable nuclear SOX11 expression. The sensitivity and specificity for SOX11 in MCL were 87.5 and 100%, respectively. Both the sensitivity and specificity for combined SOX11 and cyclin D1 immunohistochemistry were 100%.

CONCLUSION:

SOX11 immunohistochemistry could be a useful adjunct in distinguishing secondary cutaneous MCL from other CBCL.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias Cutâneas / Núcleo Celular / Linfoma de Células B / Linfoma de Célula do Manto / Fatores de Transcrição SOXC / Proteínas de Neoplasias Tipo de estudo: Diagnostic_studies / Prognostic_studies Limite: Adolescent / Adult / Aged / Aged80 / Child / Child, preschool / Female / Humans / Male / Middle aged Idioma: En Revista: J Cutan Pathol Ano de publicação: 2016 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias Cutâneas / Núcleo Celular / Linfoma de Células B / Linfoma de Célula do Manto / Fatores de Transcrição SOXC / Proteínas de Neoplasias Tipo de estudo: Diagnostic_studies / Prognostic_studies Limite: Adolescent / Adult / Aged / Aged80 / Child / Child, preschool / Female / Humans / Male / Middle aged Idioma: En Revista: J Cutan Pathol Ano de publicação: 2016 Tipo de documento: Article País de afiliação: Estados Unidos