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A Novel Case of Mammary-Type Myofibroblastoma With Sarcomatous Features
- Source :
- International Journal of Surgical Pathology. 29:308-313
- Publication Year :
- 2020
- Publisher :
- SAGE Publications, 2020.
-
Abstract
- Mammary-type myofibroblastoma (MFB) is a benign spindle cell tumor of the breast and soft tissue characterized by 13q14 alterations leading to loss of Rb-1 protein expression, a feature shared among spindle cell lipoma and cellular angiofibroma. In this article, we present a novel case of MFB arising in the left breast of a 70-year old man that microscopically showed an abrupt transition from classic MFB morphology to an area with cytologic atypia and mitotic activity, akin to sarcomatous transformation described in cellular angiofibromas. A thorough workup of the molecular underpinnings of both components using chromosomal microarray and next-generation sequencing platforms supported a clonal relationship. Nearly identical copy number changes, including a single copy loss of 13q14, were found in both components; in addition, the sarcomatous component harbored biallelic TP53 alterations. It is important for pathologists to recognize that sarcomatous features can occur in mammary-type MFB to arrive at the correct diagnosis.
- Subjects :
- Male
0301 basic medicine
Pathology
medicine.medical_specialty
DNA Copy Number Variations
Microarray
Breast Neoplasms, Male
Pathology and Forensic Medicine
Diagnosis, Differential
Neoplasms, Muscle Tissue
03 medical and health sciences
0302 clinical medicine
Biomarkers, Tumor
medicine
Humans
Breast
Mammary-Type Myofibroblastoma
Mitosis
Aged
Chromosomes, Human, Pair 13
biology
Retinoblastoma protein
medicine.disease
Neoplasms, Complex and Mixed
Angiofibromas
030104 developmental biology
030220 oncology & carcinogenesis
Spindle cell lipoma
biology.protein
Surgery
Sarcoma
Anatomy
Myofibroblastoma
Subjects
Details
- ISSN :
- 19402465 and 10668969
- Volume :
- 29
- Database :
- OpenAIRE
- Journal :
- International Journal of Surgical Pathology
- Accession number :
- edsair.doi.dedup.....4c39639b59a0cc8deba559e4a4b96bcd
- Full Text :
- https://doi.org/10.1177/1066896920947465