Endometrial stromal sarcoma of twenty cases

Background. Endometrial stromal sarcoma is a rare neoplasm. We reviewed twenty cases to study the characteristics of this disease. Methods. Twenty cases of endometrial stromal sarcoma were treated at our hospital. The clinical stage, treatment and outcome were retrospectively analyzed. Results. Endo...

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Veröffentlicht in:Acta obstetricia et gynecologica Scandinavica 1996-06, Vol.75 (6), p.551-555
Hauptverfasser: Huang, Kuang-Ta, Chen, Chi-An, Tseng, Guan-Chin, Chen, Tzer-Ming, Cheng, Wen-Fang, Hsieh, Chang-Yao
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Sprache:eng
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Zusammenfassung:Background. Endometrial stromal sarcoma is a rare neoplasm. We reviewed twenty cases to study the characteristics of this disease. Methods. Twenty cases of endometrial stromal sarcoma were treated at our hospital. The clinical stage, treatment and outcome were retrospectively analyzed. Results. Endometrial stromal sarcoma comprised 4.3% of corpus cancers and 46.4 % of uterine sarcomas at our hospital. Seven cases were stage I, one was stage II, ten were stage III, and two were stage IV at the time of diagnosis. Histopathologically, seventeen cases were classified as low-grade sarcoma and three were high-grade sarcoma. Seven patients had recurrence and five of them had already died of disease. Among these recurrent patients, one was stage II and six were stage III. All three patients with high-grade sarcoma and four with low-grade sarcoma had recurrence. Conclusions. We think mitotic count is an important prognostic factor in low-grade endometrial stromal sarcoma and high-grade endometrial stromal sarcoma has a poor prognosis even with post-operative adjuvant treatment.
ISSN:0001-6349
1600-0412
DOI:10.3109/00016349609054670