Clinicopathologic and molecular spectrum of testicular sex cord-stromal tumors not amenable to specific histopathologic subclassification.


Journal

Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc
ISSN: 1530-0285
Titre abrégé: Mod Pathol
Pays: United States
ID NLM: 8806605

Informations de publication

Date de publication:
12 2022
Historique:
received: 20 05 2022
accepted: 27 07 2022
revised: 25 07 2022
pubmed: 1 10 2022
medline: 2 12 2022
entrez: 30 9 2022
Statut: ppublish

Résumé

A subset of testicular sex cord-stromal tumors (SCST), which includes neoplasms with mixed histology, cannot be classified into a specific histologic subtype. This study evaluated the clinicopathologic, immunophenotypic and molecular features of 26 SCST not amenable to specific classification by expert uropathologists. Median age at diagnosis was 43 years and median tumor size was 2.4 cm. Follow-up information was available for 18 (69%) patients, with evidence of an aggressive clinical course in 6 patients (4 alive with disease, 2 dead of disease 3 months and 6 months after orchiectomy). Microscopically, SCST not amenable to specific classification demonstrated monophasic epithelioid (9/26, 35%), monophasic spindle cell (5/26, 19%), and biphasic or mixed histology (12/26, 46%). One or more aggressive histopathologic features were seen in 11 cases. DNA sequencing was successful in 22 tumors. Pathogenic CTNNB1 and APC alterations were seen in 7 (33%) and 2 (10%) cases, respectively, with additional variants (e.g., CDKN2A, RB1, TP53, BRCA2) being identified in individual cases. Combined evaluation of morphology, sequencing data and beta-catenin immunohistochemistry resulted in reclassification of 6 (23%) tumors as Sertoli cell tumor, not otherwise specified. This was supported by comparing the methylation profiles of a subset of these tumors and those of typical Sertoli cell tumors. Additionally, a subset of 5 neoplasms (19%) with spindle cell or biphasic histology and SMA expression was characterized by hyperdiploid genomes with recurrent chromosomal gains and absence of driver mutations, possibly representing a distinct tumor type. The SCST that remained not amenable to specific histologic classification (15/26, 58%) were enriched for aggressive histologic features and malignant clinical behavior. In conclusion, this study demonstrated that a subset of testicular SCST that were originally not amenable to specific classification could be reclassified by combined evaluation of morphology, immunohistochemistry and molecular data.

Identifiants

pubmed: 36180576
doi: 10.1038/s41379-022-01155-y
pii: S0893-3952(22)05506-5
doi:

Substances chimiques

Biomarkers, Tumor 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1944-1954

Informations de copyright

© 2022. The Author(s), under exclusive licence to United States & Canadian Academy of Pathology.

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Auteurs

Stephanie E Siegmund (SE)

Department of Pathology, Brigham and Women's Hospital/Harvard Medical School, Boston, MA, USA.

Lynette M Sholl (LM)

Department of Pathology, Brigham and Women's Hospital/Harvard Medical School, Boston, MA, USA.

Harrison K Tsai (HK)

Department of Pathology, Brigham and Women's Hospital/Harvard Medical School, Boston, MA, USA.

Yiying Yang (Y)

Department of Pathology, NYU Langone Health, New York, NY, USA.

Varshini Vasudevaraja (V)

Department of Pathology, NYU Langone Health, New York, NY, USA.

Ivy Tran (I)

Department of Pathology, NYU Langone Health, New York, NY, USA.

Matija Snuderl (M)

Department of Pathology, NYU Langone Health, New York, NY, USA.

Christopher D M Fletcher (CDM)

Department of Pathology, Brigham and Women's Hospital/Harvard Medical School, Boston, MA, USA.

Kristine M Cornejo (KM)

Department of Pathology, Massachusetts General Hospital/Harvard Medical School, Boston, MA, USA.

Muhammad T Idrees (MT)

Department of Pathology, Indiana University School of Medicine, Indianapolis, IN, USA.

Khaleel I Al-Obaidy (KI)

Department of Pathology, Indiana University School of Medicine, Indianapolis, IN, USA.

Katrina Collins (K)

Department of Pathology, Indiana University School of Medicine, Indianapolis, IN, USA.

Jennifer B Gordetsky (JB)

Department of Pathology, Vanderbilt University Medical Center/Vanderbilt University, Nashville, TN, USA.

Sara E Wobker (SE)

Department of Pathology, University of North Carolina Medical Center/University of North Carolina, Chapel Hill, NC, USA.

Michelle S Hirsch (MS)

Department of Pathology, Brigham and Women's Hospital/Harvard Medical School, Boston, MA, USA.

Kiril Trpkov (K)

Department of Pathology, Rockyview General Hospital/University of Calgary, Calgary, AB, Canada.

Asli Yilmaz (A)

Department of Pathology, Rockyview General Hospital/University of Calgary, Calgary, AB, Canada.

William J Anderson (WJ)

Department of Pathology, Brigham and Women's Hospital/Harvard Medical School, Boston, MA, USA.

Gabriela Quiroga-Garza (G)

Department of Pathology, University of Pittsburgh Medical Center Shadyside, Pittsburgh, PA, USA.

Cristina Magi-Galluzzi (C)

Department of Pathology, The University of Alabama at Birmingham, Birmingham, Alabama, UK.

Sofia Canete-Portillo (S)

Department of Pathology, The University of Alabama at Birmingham, Birmingham, Alabama, UK.

Andres M Acosta (AM)

Department of Pathology, Brigham and Women's Hospital/Harvard Medical School, Boston, MA, USA. aacosta4@bwh.harvard.edu.

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