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Chondrosarcoma of the uterus: case report and literature review.

作者信息

Namizato Claudia Sofia, Muriel-Cueto Pedro, Baez-Perez Jose Maria, Bartha Jose Luis, Hervias-Vivancos Blas

机构信息

Department of Obstetrics and Gynecology, University Hospital Puerta del Mar, Avenida Ana de Viya 21, 11009 Cádiz, Spain.

出版信息

Arch Gynecol Obstet. 2008 Oct;278(4):369-72. doi: 10.1007/s00404-008-0595-6. Epub 2008 Feb 20.

Abstract

BACKGROUND

Pure heterologous sarcomas of the uterine corpus are extremely rare, accounting for 4% of all uterine sarcomas. Primary chondrosarcoma, which is characterized by the absence of epithelial or other heterologous mesenchymal elements, is included in this group. To this date, only 17 cases, including the presenting case, have been reported.

CASE

A 55-year-old female presenting with post-menopausal bleeding was diagnosed with chondrosarcoma of the uterus, after abdominal hysterectomy and bilateral salpingoophorectomy. After 8 months of surgery, there is no evidence of recurrence after receiving external radiotherapy and brachytherapy.

CONCLUSION

Primary chondrosarcoma of the uterus is an extremely rare uterine tumour most frequently diagnosed by the pathologist. They are usually aggressive malignant tumours with an early relapse and metastases.

摘要

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