Background: Due to the rarity of gastric leiomyosarcomas, only little
is known on the results of diagnostics and therapy of these tumors. Ac
cording to literature, the problem of suitable criteria in determining
malignancy of these neoplasms is unsettled. Patients and Method: 21 p
atients (10 male, 11 female, aged 13 to 74 [53 +/- 13,9] years) with l
eiomyosarcomas of the stomach were treated from 1978 to 1993. In a ret
rospective study, the diagnostic and therapeutic results and the patho
logic features of these patients are compared with the results of lite
rature.Results: Diagnosis was rarely confined preoperatively. Potentia
lly curative resection was possible in 13/21 cases. Five year survival
was 44% overall (RD-resections: 60%, R1/2-resections 22%) with a wide
spread of individual cases. Pathologic examination of the tumors show
ed only half of the tumors classifiable according to the system of McG
rath. Some well differentiated tumors revealed unclear malignancy crit
eria. Analysis of prognostic factors showed no statistically significa
nt influence of surgical radicality but a significant influence of tum
or size, mitotic activity and nuclear grading on survival and recurren
ce. Conclusion: Because of their rare incidence, the treatment of gast
ric leiomyosarcomas remains non-standardized. Surgical radical removal
of the tumor seems to promise the largest benefit. The treatment of p
atients with a residual or recurrent tumors remains individual, no adj
uvant radio- or chemotherapeutical treatment can be generally recommen
ded.