MRI features of cellular angiomyofibroma with pathologic correlation
Phillip J Koo1, Igor Goykhman, Larissa Lembert
1Department of Radiology, Pennsylvania Hospital of the University of Pennsylvania Health System, Philadelphia, Pennsylvania 19107, USA. koop@uphs.upenn.edu
Journal of Magnetic Resonance Imaging : JMRI
|April 24, 2009
Summary
Cellular angiofibroma, a rare tumor, was found in a 60-year-old male's scrotum. This case details the first reported MRI findings for this extratesticular mesenchymal tumor.
Area of Science:
- Oncology
- Radiology
- Pathology
Background:
- Cellular angiofibroma (CAF), also known as angiomyofibroblastoma-like tumor, is a rare mesenchymal neoplasm.
- Historically, CAF has been described predominantly in the female vulva, perineum, and pelvis.
- Extratesticular mesenchymal tumors encompass a range of rare lesions within the scrotum and perineum.
Observation:
- This report details a rare case of a 60-year-old male presenting with a firm, palpable scrotal mass.
- The mass was diagnosed as a cellular angiofibroma, occurring adjacent to a scrotal lipoma.
- This represents a unique presentation of CAF in a male extratesticular location.
Findings:
- The study presents the magnetic resonance imaging (MRI) features of a cellular angiofibroma in a male patient.
- These MRI findings are correlated with the known pathological characteristics of CAF.
- The imaging demonstrates a benign cellular and fibrous tumor with significant vascularity.
Implications:
- This case expands the known anatomical distribution of cellular angiofibroma to include the male scrotum.
- The presented MRI findings are novel and contribute to the radiological understanding of this rare tumor.
- Accurate radiological characterization is crucial for the diagnosis and management of extratesticular masses.
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