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Arch Pathol Lab Med ; 143(9): 1119-1125, 2019 09.
Artigo em Inglês | MEDLINE | ID: mdl-30838879

RESUMO

CONTEXT.­: Metastatic mucinous tumors present a diagnostic challenge for pathologists as tumor histomorphology is often nonspecific and optimal immunoprofiles are still under investigation. OBJECTIVE.­: To present a head-to-head comparison of special AT-rich sequence-binding protein 2 (SATB2) and caudal type homeobox 2 (CDX2) expression in a diverse array of primary mucinous tumors. DESIGN.­: SATB2 and CDX2 immunohistochemical stains were performed on whole sections from 44 mucinous colorectal carcinomas and 175 noncolorectal mucinous tumors. A nuclear scoring system measuring intensity (0-3+) and percentage staining (0 = <5%, 1 = 5%-49%, 2 = ≥50%) was implemented, producing an additive histologic score (H-score). RESULTS.­: SATB2 demonstrated acceptable accuracy at low to moderate expression levels (H-scores of 1-4). With these H-score cutoffs, overall accuracy was greater than 90%. In contrast, CDX2's accuracy rivaled that of SATB2 only at an H-score of 5 (89.0%), as its specificity suffered at lower expression levels (<70.0% at H-scores of 1-4). Using a moderate H-score cutoff of 3 or higher, significant differences for both sensitivity and specificity were identified between SATB2 and CDX2 (P = .01 for sensitivity and P < .001 for specificity), though these stains were near equivalent when each was interpreted as positive at its respective optimal H-score (SATB2 ≥ 3 and CDX2 = 5). CONCLUSIONS.­: SATB2 is a more accurate marker of colorectal origin across a variety of expression levels compared with CDX2 when applied to mucinous tumors from a host of primary sites. However, these stains are near equivalent when each is interpreted at its optimal expression level.


Assuntos
Adenocarcinoma Mucinoso/diagnóstico , Fator de Transcrição CDX2/análise , Neoplasias Colorretais/diagnóstico , Proteínas de Ligação à Região de Interação com a Matriz/análise , Metástase Neoplásica/diagnóstico , Fatores de Transcrição/análise , Adenocarcinoma Mucinoso/patologia , Neoplasias Colorretais/patologia , Diagnóstico Diferencial , Humanos , Imuno-Histoquímica/métodos , Metástase Neoplásica/patologia , Sensibilidade e Especificidade
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