Bilateral Phyllodes Giant Tumor. A Case Report Analyzed by Array-CGH.

array-CGH breast tumor phyllodes tumor

Journal

Diagnostics (Basel, Switzerland)
ISSN: 2075-4418
Titre abrégé: Diagnostics (Basel)
Pays: Switzerland
ID NLM: 101658402

Informations de publication

Date de publication:
15 Oct 2020
Historique:
received: 18 09 2020
revised: 07 10 2020
accepted: 09 10 2020
entrez: 20 10 2020
pubmed: 21 10 2020
medline: 21 10 2020
Statut: epublish

Résumé

The breast phyllodes tumor is a biphasic tumor that accounts for less than of 1% of all breast neoplasms. It is classified as benign, borderline, or malignant, and can mimic benign masses. Some recurrent alterations have been identified. However, a precise molecular classification of these tumors has not yet been established. Herein, we describe a case of a 43-year-old woman that was admitted to the emergency room for a significant bleeding from the breast skin. A voluminous ulcerative mass of the left breast and multiple nodules with micro-calcifications on the right side were detected at a physical examination. A left total mastectomy and a nodulectomy of the right breast was performed. The histological diagnosis of the surgical specimens reported a bilateral giant phyllodes tumor, showing malignant features on the left and borderline characteristics associated with a fibroadenoma on the right. A further molecular analysis was carried out by an array-Comparative Genomic Hybridization (CGH) to characterize copy-number alterations. Many losses were detected in the malignant mass, involving several tumor suppressor genes. These findings could explain the malignant growth and the metastatic risk. In our study, genomic profiling by an array-CGH revealed a greater chromosomal instability in the borderline mass (40 total defects) than in the malignant (19 total defects) giant phyllodes tumor, reflecting the tumor heterogeneity. Should our results be confirmed with more sensitive and specific molecular tests (DNA sequencing and FISH analysis), they could allow a better selection of patients with adverse pathological features, thus optimizing and improving patient's management.

Identifiants

pubmed: 33076253
pii: diagnostics10100825
doi: 10.3390/diagnostics10100825
pmc: PMC7602371
pii:
doi:

Types de publication

Case Reports

Langues

eng

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Auteurs

Francesco Fortarezza (F)

Department of Cardiac, Thoracic, Vascular Sciences and Public Health, Pathology Unit, University of Padova, 35121 Padova, Italy.

Federica Pezzuto (F)

Department of Cardiac, Thoracic, Vascular Sciences and Public Health, Pathology Unit, University of Padova, 35121 Padova, Italy.

Gerardo Cazzato (G)

Department of Emergency and Organ Transplantation (DETO), Pathology Section, Breast Unit Care, University of Bari, Medical School, 70124 Bari, Italy.

Clelia Punzo (C)

Department of Emergency and Organ Transplantation (DETO), Surgery Section, Breast Unit Care, University of Bari, Medical School, 70124 Bari, Italy.

Antonio d'Amati (A)

Department of Emergency and Organ Transplantation (DETO), Pathology Section, Breast Unit Care, University of Bari, Medical School, 70124 Bari, Italy.

Teresa Lettini (T)

Department of Emergency and Organ Transplantation (DETO), Pathology Section, Breast Unit Care, University of Bari, Medical School, 70124 Bari, Italy.

Mattia Gentile (M)

Medical Genetics, "Di Venere" Hospital, 70131 Carbonara (Bari), Italy.

Antonia Lucia Buonadonna (AL)

Medical Genetics, "Di Venere" Hospital, 70131 Carbonara (Bari), Italy.

Marta Mariano (M)

Department of Emergency and Organ Transplantation (DETO), Pathology Section, Breast Unit Care, University of Bari, Medical School, 70124 Bari, Italy.

Angela Pezzolla (A)

Department of Emergency and Organ Transplantation (DETO), Surgery Section, Breast Unit Care, University of Bari, Medical School, 70124 Bari, Italy.

Gabriella Serio (G)

Department of Emergency and Organ Transplantation (DETO), Pathology Section, Breast Unit Care, University of Bari, Medical School, 70124 Bari, Italy.

Classifications MeSH