# ‘Malignant granular cell tumor of the Appendiceal orifice: a rare case and review of literature’

## TL;DR

A rare case of malignant granular cell tumor at the appendiceal orifice is reported, highlighting the need for early detection and surgical intervention.

## Contribution

This paper presents a rare clinical case of malignant GCT in the colon and emphasizes its management.

## Key findings

- A 37-year-old woman was diagnosed with a malignant granular cell tumor at the appendiceal orifice.
- Surgical resection with clear margins was performed, and histopathology confirmed malignancy.
- The case underscores the importance of early detection to prevent severe outcomes in malignant GCTs.

## Abstract

Granular cell tumors (GCTs) are rare, mostly benign soft-tissue neoplasms, with only 8% occurring in the gastrointestinal tract, making the colon an uncommon location. We present the case of a 37-year-old Hispanic woman who underwent a screening colonoscopy due to a family history of colon cancer. A submucosal nodule at the appendiceal orifice was resected, and a biopsy revealed a malignant GCT, confirmed by S100-positive staining. The patient underwent a right hemicolectomy, with the resection showing a 2 mm focus of granular cell tumor with clear margins. Histopathology confirmed malignancy, with additional findings of reactive hyperplasia of mucosa-associated lymphoid tissue and focal ileitis. Although rare in the colon, malignant GCTs carry a high risk of mortality and recurrence. Small lesions (< 1 cm) can be monitored, but larger or malignant ones require surgical resection. Our case emphasizes the importance of early detection and intervention to prevent severe outcomes in malignant GCTs.