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Synchronous subcutaneous granular cell tumours, a rare presentation.
1Department of Surgery, Albert Einstein Healthcare Network , Philadelphia, PA , United States.
This case highlights a rare, multifocal granular cell tumor presentation in a 36-year-old woman. Surgical excision confirmed benign granular cell tumors, emphasizing the need for definitive pathology in diagnosis.
Area of Science:
- Oncology
- Pathology
- Dermatology
Background:
- Granular cell tumors (GCTs) are rare, typically benign neoplasms derived from Schwann cells.
- They most commonly occur in the head and neck region and are usually asymptomatic.
Observation:
- A 36-year-old woman presented with a large, symptomatic left flank mass and multiple synchronous subcutaneous masses on the breast, auricle, and cheek.
- Initial diagnosis was confirmed as granular cell tumor via core needle biopsy.
Findings:
- Histopathological and immunohistochemical analysis of excised masses confirmed non-malignant granular cell tumors.
- Multifocal GCTs are present in 5-16% of patients, though this presentation with extensive subcutaneous involvement is unique.
- Malignancy, rare in GCTs (approx. 2%), is indicated by high mitotic rate, necrosis, and pleomorphism.
Implications:
- Definitive histopathological diagnosis is crucial for granular cell tumors, as frozen section analysis is often unhelpful.
- Surgical resection is the primary treatment for symptomatic GCTs, followed by surveillance.
- This case expands the understanding of GCT presentation and multifocality.
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