BCOR Expression in Mullerian Adenosarcoma: A Potential Diagnostic Pitfall.


Journal

The American journal of surgical pathology
ISSN: 1532-0979
Titre abrégé: Am J Surg Pathol
Pays: United States
ID NLM: 7707904

Informations de publication

Date de publication:
06 2020
Historique:
pubmed: 6 2 2020
medline: 21 10 2020
entrez: 4 2 2020
Statut: ppublish

Résumé

Adenosarcoma can mimic high-grade endometrial stromal sarcoma with ZC3H7B-BCOR fusion that may show entrapped glands and often exhibits diffuse BCOR expression. We encountered diffuse BCOR expression in rare adenosarcomas and sought to define its frequency among a larger cohort of these tumors. BCOR immunohistochemistry was performed on archival formalin-fixed paraffin-embedded tumor tissue in 13 of 14 adenosarcomas with and without stromal overgrowth arising in the uterus or ovary. The staining intensity and percentage of positive tumor nuclei in the mesenchymal component were evaluated. Eleven cases with sufficient tumoral tissue were subjected to fluorescence in situ hybridization for the detection of BCOR, BCORL1, NUTM1, ZC3H7B, and JAZF1 rearrangement. Three cases were subjected to targeted RNA sequencing. BCOR was expressed in 9 of 13 (70%) tumors, including 6 with and 3 without stromal overgrowth. Moderate to strong staining in >70% of cells was seen throughout in 1 low-grade and 6 high-grade tumors, 5 of which had stromal overgrowth. No staining was seen in 3 low-grade and 1 high-grade tumors with stromal overgrowth. One tumor demonstrating extensive sex cord-like differentiation and diffuse BCOR expression harbored JAZF1 and BCORL1 rearrangements. No BCOR or BCORL1 rearrangement was identified in the remaining tumors. BCOR expression is seen in most adenosarcomas with and without stromal overgrowth. BCORL1 rearrangement is seen in rare tumors with diffuse BCOR expression. Assessment of BCOR or BCORL1 rearrangement status is required in adenosarcomas demonstrating BCOR expression.

Identifiants

pubmed: 32011345
doi: 10.1097/PAS.0000000000001445
pii: 00000478-202006000-00006
pmc: PMC10189887
mid: NIHMS1548644
doi:

Substances chimiques

BCOR protein, human 0
Biomarkers, Tumor 0
Proto-Oncogene Proteins 0
Repressor Proteins 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

765-770

Subventions

Organisme : NCI NIH HHS
ID : P30 CA008748
Pays : United States

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Auteurs

Vidarshi Muthukumarana (V)

Department of Pathology, University of Texas Medical Branch, Galveston, TX.

Daniel J Fix (DJ)

Department of Pathology, Hackensack University Medical Center, Hackensack, NJ.

Simona Stolnicu (S)

Department of Pathology, University of Medicine, Pharmacy, Sciences and Technology of Targu Mures, Targu Mures, Romania.

Kay J Park (KJ)

Department of Pathology, Memorial Sloan Kettering Cancer Center, New York City, NY.

Robert A Soslow (RA)

Department of Pathology, Memorial Sloan Kettering Cancer Center, New York City, NY.

Ryma Benayed (R)

Department of Pathology, Memorial Sloan Kettering Cancer Center, New York City, NY.

Marc Ladanyi (M)

Department of Pathology, Memorial Sloan Kettering Cancer Center, New York City, NY.

Cristina R Antonescu (CR)

Department of Pathology, Memorial Sloan Kettering Cancer Center, New York City, NY.

Sarah Chiang (S)

Department of Pathology, Memorial Sloan Kettering Cancer Center, New York City, NY.

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Classifications MeSH