A primary gastric synovial sarcoma A case report and literature review
- Author(s)
- In Tae So; Kwang Bum Cho; Ju Yup Lee; Sang Jin Kim; Hye In Jung; Jong Hwan Choi; Yoo Jin Lee; Hyun Jik Lee; Kyung Sik Park; Seung Wan Ryu; Yu Na Kang
- Keimyung Author(s)
- Cho, Kwang Bum; Park, Kyung Sik; Ryu, Seung Wan; Lee, Yoo Jin; Kang, Yu Na; Lee, Ju Yup
- Department
- Dept. of Internal Medicine (내과학)
Dept. of Surgery (외과학)
Dept. of Pathology (병리학)
- Journal Title
- Medicine
- Issued Date
- 2017
- Volume
- 96
- Issue
- 49
- Keyword
- endoscopy; gastric neoplasm; synovial sarcoma
- Abstract
- RATIONALE:
When a gastric spindle cell tumor is observed, the possibility of synovial carcinoma, besides common mesenchymal tumor, should also be considered.
PRESENTING CONCERNS OF THE PATIENT:
The patient is a 51-year-old American woman who underwent medical check-up at a general hospital. Upper endoscopy showed a 2-cm sized mass covered with intact mucosa, and a central depression located on the posterior wall of the mid body. Biopsy of the mass showed focal atypical cells proliferation in mucosa on hematoxylin & eosin (H&E) staining. Endoscopic ultrasound showed a 17-mm homogenously hypoechoic mass within the submucosal layer.
INTERVENTIONS:
After diagnostic endoscopic submucosal dissection was performed, H&E and immunohistochemical staining showed synovial sarcoma (SS). To confirm the diagnosis, reverse transcriptase-polymerase chain reaction was performed, revealing a chimeric transcript of the SYT-SSX1 fusion gene. The diagnosis of primary gastric SS was confirmed because no evidence of possible primary lesions or metastatic lesions was observed. Therefore, the patient underwent distal gastrectomy.
OUTCOMES:
After surgery, the surgical specimen demonstrated no residual tumor cells. The patient received no adjuvant therapy, and there has been no evidence of local recurrence or distant metastasis for 2 months after the operation.
LESSONS:
When gastric subepithelial tumor is suspicious, we should also consider gastric SS.
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