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首页> 外文期刊>International Journal of Reproduction, Contraception, Obstetrics and Gynecology >Embryonal rhabdomyosarcoma of the uterine cervix: a rare case report
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Embryonal rhabdomyosarcoma of the uterine cervix: a rare case report

机译:子宫颈胚胎横纹肌肉瘤:罕见病例报告

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Embryonal rhabdomyosarcoma of the female genital tract is a rare tumour. It tends to occur during childhood in the vagina and, rarely, it can arise in the uterine cervix, with a peak incidence in the second decade. We report a case of a 18-year-old female with an embryonal rhabdomyosarcoma (sarcoma botryoides) presenting himself as a cervical polyp. This tumour consisted of rhabdomyoblasts with miscellaneous differentiation surrounded by a loose, myxoid stroma. The patient was successfully treated with cervical conization and adjuvant chemotherapy. She is now disease-free at the 28th month follow-up. Awareness of this uncommon lesion in the cervix and its clinical implications is important to prevent misdiagnosis. Therapy has recently inclined to conservative and fertility-sparing treatment.
机译:女性生殖道的胚性横纹肌肉瘤是一种罕见的肿瘤。它倾向于在童年时期的阴道中发生,很少发生在子宫颈中,在第二个十年中发病率最高。我们报告了一例一名18岁女性,患有胚胎性横纹肌肉瘤(肉瘤性葡萄胎),表现为宫颈息肉。该肿瘤由横纹肌母细胞组成,其具有杂种分化,周围是疏松的粘液样基质。该患者已成功接受宫颈锥切术和辅助化疗。现在她在第28个月的随访中没有疾病。意识到子宫颈的这种罕见病变及其临床意义对于防止误诊很重要。近来,治疗倾向于保守和节约生育的治疗。

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