Synovial sarcoma of the stomach

Definition

Synovial sarcoma most commonly occurs in soft tissues of the extremities. Rarely, an identical tumour has been reported as occurring as a primary neoplasm in the stomach.

Epidemiology

This is a tumour of adults with a wide age range.

Clinical features

Patients present with upper gastrointestinal haemorrhage, dysphagia, or an abdominal mass.

Macroscopic appearances

The tumour may form a polypoidal mass or ulcer. There may be calcification.

Histopathology

Tumours extend from the mucosa into muscualris propria. In the monophasic fibrous type of synovial sarcoma, the spindle cells form haphazard sheets with variable amounts of collagen. Poorly differentiated tumours show round cells with a high mitotic rate. Biphasic tumours include an epithelial components composed of cuboidal cells forming glands and solid sheets. There may be osseous metaplasia.

Immunohistochemistry

 

 

spindle cell component

epithelial cells

 

AE1/AE3

9/91

1/11

Cytokeratin 7

5/51

1/11

EMA

9/91

1/11

vimentin

4/41

 

SMA

1/41

 

CD56

1/11

 

CD99

9/91

 

S100

0/41

 

CD34

0/51

 

CD117

0/81

 

Desmin

0/41

 

     

Molecular studies

All seven cases (6 monophasic, 1 biphasic) tested showed SYT-SSX fusion transcripts1.

Differential diagnosis

Management

Surgical excision.

Prognosis

Early plaque-like tumours may have a relatively good prognosis1.

References

1 Makhlouf HR, Ahrens W, Agarwal B, et al. Synovial sarcoma of the stomach: a clinicopathologic, immunohistochemical, and molecular genetic study of 10 cases. Am J Surg Pathol 2008; 32:275-81

This page last revised 22.3.2008

©SMUHT/PW Bishop