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Atypical esophageal granular cell tumor: Case report
Zineb Benchekroun1, Amal Akammar1, Hajar Bennani1
1Department of radiology, CHU HASSAN II FES, Morocco.
Radiology Case Reports
|November 8, 2021
Summary
Esophageal granular cell tumors (GCTs), rare benign neoplasms, can rarely transform into malignant forms. This case highlights an uncommon esophageal GCT presentation, emphasizing vigilance for potential malignant changes.
Area of Science:
- Gastroenterology
- Oncology
- Pathology
Background:
- Esophageal granular cell tumors (GCTs), also known as Abrikossoff's tumors, are rare neoplasms originating from Schwann cells.
- While typically benign, a small percentage (2-3%) of GCTs can undergo malignant transformation.
- GCTs most commonly occur in the skin, subcutaneous tissue, and tongue, with 5-8% arising in the gastrointestinal tract, and one-third of these in the esophagus.
Observation:
- A 70-year-old male presented with a 3-month history of dysphagia.
- Diagnostic workup involving endoscopy and CT scans presented challenges in diagnosis.
- Histopathology and immunohistochemistry confirmed the presence of granular cells, establishing the diagnosis of esophageal GCT.
Findings:
- The case involved an uncommon presentation of an Abrikossoff's tumor in the esophagus.
- The histopathological and immunohistochemical analyses were crucial for confirming the diagnosis.
- The tumor's evolution served as a clinical observation for potential malignant transformation.
Implications:
- This case underscores the importance of considering malignant transformation in esophageal GCTs, even though they are typically benign.
- Early and accurate diagnosis through histopathology and immunohistochemistry is critical for appropriate patient management.
- Further literature review and case reporting are valuable for understanding the behavior and potential risks associated with esophageal GCTs.
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