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Sigmoid colon Schwannoma simulating colon cancer
María de Armas Conde1, Ana Soto Sánchez2, Moisés Hernández Barroso2
1Cirugía General y del Aparato Digestivo, Hospital Universitario Nuestra Señora de la Candelaria, España.
Revista Espanola De Enfermedades Digestivas
|March 14, 2022
Summary
Gastrointestinal schwannomas are rare tumors. Diagnosis is challenging due to their submucosal location, often requiring S-100 immunohistochemistry for confirmation.
Area of Science:
- Gastroenterology
- Surgical Oncology
- Pathology
Background:
- Schwannomas are rare gastrointestinal tumors, accounting for 2-6% of all gastrointestinal tumors.
- Approximately 12% of gastrointestinal schwannomas occur in the small and large intestines.
Observation:
- An 87-year-old woman presented with epigastric pain and dyspepsia.
- CT scan and colonoscopy revealed a neoplastic process in the sigmoid colon.
- Laparoscopic sigmoidectomy was performed, with histological examination confirming a schwannoma.
Findings:
- Schwannomas are submucosal lesions, making endoscopic biopsy challenging as it typically samples only the mucosa.
- Differential diagnosis includes gastrointestinal stromal tumors (GIST) and leiomyomas.
- Immunohistochemistry is crucial: positive for S-100 and negative for C-KIT, CD-34, actin, and desmin aids in differentiating schwannoma from GIST and leiomyoma.
Implications:
- Accurate diagnosis of gastrointestinal schwannoma is difficult due to nonspecific radiological findings and challenges with endoscopic biopsies.
- S-100 positive immunohistochemistry in histological studies is essential for confirming schwannoma diagnosis.
- Understanding these diagnostic challenges is vital for appropriate patient management and treatment strategies.
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