Case Report Open Access
Copyright ©The Author(s) 2004. Published by Baishideng Publishing Group Inc. All rights reserved.
World J Gastroenterol. Aug 15, 2004; 10(16): 2452-2454
Published online Aug 15, 2004. doi: 10.3748/wjg.v10.i16.2452
Granular cell tumor of colon: Report of a case and review of literature
Dae-Kyung Sohn, Hyo-Seong Choi, Yeon-Soo Chang, Jin-Myeong Huh, Dae-Hyun Kim, Dae-Yong Kim, Young-Hoon Kim, Hee-Jin Chang, Kyung-Hae Jung, Seung-Yong Jeong, Research Institute and Hospital, National Cancer Center, Goyang, Gyeonggi 411-769, Korea
Author contributions: All authors contributed equally to the work.
Correspondence to: Dr. Seung-Yong Jeong, Center for Colorectal Cancer, Research Institute and Hospital, National Cancer Center, 809 Madu-dong, Ilsan-gu, Goyang, Gyeonggi 411-769, Korea. syjeong@ncc.re.kr
Telephone: +82-31-920-1632 Fax: +82-31-920-0002
Received: March 15, 2004
Revised: March 26, 2004
Accepted: April 9, 2004
Published online: August 15, 2004

Abstract

Granular cell tumor (GCT) is uncommon in the colon and rectum. Here we report a case of GCT in the transverse colon. A 48-year-old male patient underwent a screening colonoscopy. A yellowish sessile lesion, about 4 mm in diameter, was found in the transverse colon. An endoscopic snare resection was performed without complication. Histological examination revealed the tumor consisted of plump neoplastic cells with abundant granular eosinophilic cytoplasm containing acidophilic periodic acid Schiff-positive, diastase-resistant granules. Immunohistochemical analysis showed the tumor cells expressed S-100 protein and neuron-specific enolase. Thus, the resected tumor was diagnosed as a GCT. Since GCTs are usually benign, endoscopic resection constitutes an easy and safe treatment. Colonoscopists should consider the possibility of GCT in the differential diagnosis of submucosal tumors of the colon.




INTRODUCTION

Granular cell tumor (GCT) is relatively rare soft tissue tumor that can be located anywhere in the body. It commonly occurs in oral cavities and subcutaneous tissues, but is uncommon in the colon and rectum[1,2]. In the gastrointestinal tract, the most common site for GCT is the esophagus, followed by the duodenum, anus and stomach[3,4]. This usually benign tumor appears as a submucosal nodule, measuring less than 2 cm in diameter, and is often found incidentally during colorectal examinations[2-6]. Here we report a case of a 48-year-old man diagnosed with a GCT arising in the transverse colon and treated by endoscopic resection.

CASE REPORT

A 48-year-old man was admitted for a screening colonoscopy. He had been healthy without specific complaints, family or past medical history. At the time of colonoscopy, a yellowish, hemispheric nodule 4 mm in diameter, was found in the transverse colon. It was a firm nodule covered by intact mucosa (Figure 1). The patient underwent an endoscopic snare resection, was observed for 30 min, and then discharged. There was no immediate or delayed complication.

Figure 1
Figure 1 A hemispheric, yellowish submucosal tumor with intact mucosa, about 4 mm in diameter in transverse colon revealed by endoscopy.

Histological examination of the resected tissue revealed a submucosal tumor composed of solid masses of plump histiocyte-like tumor cells with abundant granular eosinophilic cytoplasm containing acidophilic periodic acid Schiff (PAS)-positive, diastase-resistant granules (Figure 2). Immunohistochemical analysis showed the tumor cells expressed S-100 protein and neuron-specific enolase (NSE) (Figure 3), but were negative for desmin and cytokeratin. The resected tumor was diagnosed as a GCT occurring in the transverse colon.

Figure 2
Figure 2 A submucosal tumor revealed by histological examination in resected tissue. A: Resected lesion showing a submucosal tumor covered with normal mucosa (HE staining, × 40). B: Higher magnification view of the tumor (HE staining, left: × 100; right: × 200).
Figure 3
Figure 3 Diffuse and strong expression of S-100 protein in tumor shown by immunohistochemical examination (Original magnification: × 100).
DISCUSSION

GCT, first described by Abrikossoff in 1926[7], may arise virtually anywhere in the body, but was seldomly found in the gastrointestinal tract[1,2]. In most cases, gastrointestinal GCTs were found incidentally during endoscopy, and appeared as small, round submucosal nodules covered by normal mucosa[1-5,8-10]. GCTs have also been detected in the muscle layer of the gastrointestinal tract and in subserosal areas, although such findings were uncommon[2,4,11].

Endo et al[10] reported 33 cases of colorectal GCT in Japan, and Rossi et al[8] reported 55 patients diagnosed with GCTs of the colon. To date, 7 cases of colonic GCT have been reported in Korean literature (Table 1). This excludes two cases of perianal GCT which may have arisen from perianal skin rather than anal mucosa. Except for one rectal case, all 6 colonic GCTs reported in Korea were located in the proximal colon - ascending colon, transverse colon and cecum including the appendix. The male-to-female ratio was 1:1.3 and the mean age was 41.0 ± 6.5 years (range 31-49 years). Bowel resection was the treatment administered for the 2 cases diagnosed before 1985, while endoscopic removal of the tumor was performed in the later cases. Advances in endoscopic diagnosis and resection probably led to the alteration in treatment approach for the latter cases.

Table 1 Summary of 7 cases of colorectal granular cell tumor reported in Korea.
NYearAuthorSex/AgeLocationSize (cm)Treatment
11982Kim et al[12]F/44Cecum1.5 × 1.5Surgery
21983Lee et al[13]F/31Cecum1.0Surgery
31991Choi et al[14]F/39A-colon0.9 × 0.8Polypectomy
42000Kim et al [15]M/40Appendix0.7Polypectomy
52003Lee et al[16]F/36A-colon1.5 × 0.6Polypectomy
62003Kim et al[17]M/49Rectum0.7Polypectomy
7The present caseM/48T-colon0.4 × 0.3Polypectomy

GCT could seldomly be diagnosed based on macroscopic and endoscopic examination due to both its small size and its shape resembling a diminutive polyp[1]. Recently, endoscopic ultrasound has been frequently used for determining the depth of tumor invasion in the gastrointestinal wall, and is also useful for evaluating gastrointestinal submucosal tumors[9,10,18]. However, in the present case, it was difficult to suspect GCT because the endoscopic features of the tumor resembled those of a small sessile polyp. We performed one-stage endoscopic snare polypectomy during screening colonoscopy.

The final diagnosis of GCT depends on pathological findings. The histological markers for GCT are: (1) plump histiocyte-like, bland-looking neoplastic cells with abundant granular eosinophilic cytoplasm containing acidophilic, PAS-positive, diastase-resistant granules; (2) small, uniform nuclei, in which mitotic figures are absent; (3) neural markers, including S-100 protein or NSE expressed uniformly[10,19-22]. In the present patient, the histological findings on the resected specimen were typical of a GCT.

Although GCTs are usually benign, some malignant GCT cases have been reported. Malignancy has been found to correlate with tumor size, more than 60% of metastatic GCTs were larger than 4 cm in diameter[6,11,23]. However, in most colonic GCTs, the tumor size was less than 2 cm and the tumor was well separated from the muscularis propia. Since this tumor is considered to be usually benign, endoscopic removal has been the most appropriate choice of treatment for colonic GCT[2,8,10,24].

In conclusion, we report a case of GCT in the transverse colon. The tumor was removed by endoscopic resection and the patient was discharged without complication. GCTs of the colon can be found incidentally during colonoscopy, and endoscopic removal of the tumor is the safest and most feasible treatment. Colonoscopists should consider the possibility of GCT in the differential diagnosis of submucosal tumors of the colon.

Footnotes

Edited by Wang XL Proofread by Chen WW and Xu FM

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