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A huge abdominal mass mimicking ovarian cancer: p53-negative but aneuploid myxoid leiomyosarcoma of the uterus.
Kaleli, S; Calay, Z; Ceydeli, N; Aydýnlý, K; Kösebay, D.
  • Kaleli S; Department of Obstetrics and Gynecology, Cerrahpapa Medical School, Ystanbul University, P.O. Box 11, Cerrahpapa, Fatih, Ystanbul, Turkey. semihkaleli@yahoo.com
Eur J Obstet Gynecol Reprod Biol ; 100(1): 96-9, 2001 Dec 10.
Article en En | MEDLINE | ID: mdl-11728667
ABSTRACT

OBJECTIVE:

Less than 20 myxoid leiomyosarcoma cases were reported in literature. Since, these tumors are very rare and may exhibit highly malignant behavior despite their low mitotic index, clinical course and optimum type of therapy of myxoid variant of leiomyosarcoma were not well understood. The goal of this report is to contribute the better understanding of this rare type of tumor.

METHODS:

A 39-year-old woman presented with a huge abdominal cystic mass. Laparotomy was performed and frozen section diagnosis was low-grade uterine leiomyosarcoma. TAH-BSO, omentectomy, pelvic lymph node and peritoneal samplings were carried out. No chemotherapy was performed after surgical therapy.

RESULTS:

Final histopathological diagnosis was uterine myxoid leiomyosarcoma. The tumor was p53-negative and had aneuploid DNA content. The patient tolerated well the operation and she is alive and free of disease after 24 months of primary surgical treatment.

CONCLUSION:

Uterine myxoid leiomyosarcoma may present a huge abdominal cystic mass and can be treated successfully with surgery alone.
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Banco de datos: MEDLINE Asunto principal: Neoplasias Ováricas / Neoplasias Uterinas / Proteína p53 Supresora de Tumor / Aneuploidia / Leiomioma Tipo de estudio: Diagnostic_studies Límite: Adult / Female / Humans Idioma: En Año: 2001 Tipo del documento: Article
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Banco de datos: MEDLINE Asunto principal: Neoplasias Ováricas / Neoplasias Uterinas / Proteína p53 Supresora de Tumor / Aneuploidia / Leiomioma Tipo de estudio: Diagnostic_studies Límite: Adult / Female / Humans Idioma: En Año: 2001 Tipo del documento: Article