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Paratesticular superficial angiomyxomas: A case report
1Department of Urology, People's Hospital of Pengshan District, Meishan, Sichuan, China.
Superficial angiomyxoma (SA) is a rare tumor. Complete surgical resection is recommended to prevent recurrence, as demonstrated by a successful paratesticular SA case with no recurrence after 3 years.
Area of Science:
- Dermatology
- Pathology
- Surgical Oncology
Background:
- Superficial angiomyxoma (SA) is a rare benign neoplasm originating in the superficial dermis or subcutaneous tissue.
- Characterized by abundant myxoid stroma and vascularity, SA typically presents as nodules on the trunk, head, or limbs.
- Literature review reveals a scarcity of reported cases, highlighting the rarity of this condition.
Purpose of the Study:
- To present a rare case of paratesticular superficial angiomyxoma in a 43-year-old male.
- To detail the diagnostic process and surgical management of this unusual presentation.
- To share therapeutic experience and emphasize strategies for preventing recurrence.
Main Methods:
- Surgical excision of the paratesticular mass.
- Histopathological analysis using hematoxylin and eosin staining for myxoid stroma.
- Immunohistochemical staining (CD34, desmin, estrogen receptor, vimentin, S-100) for differential diagnosis.
Main Results:
- Histopathology confirmed abundant myxoid stroma.
- Immunohistochemistry results supported the diagnosis of superficial angiomyxoma.
- The tumor was completely excised with a well-defined boundary.
- No recurrence was observed during a 3-year follow-up period.
Conclusions:
- Complete surgical resection, potentially including a margin of normal tissue, is crucial for preventing superficial angiomyxoma recurrence.
- This case underscores the importance of thorough histopathological and immunohistochemical evaluation for accurate diagnosis.
- Successful complete excision led to a favorable long-term outcome without recurrence.
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