子宫颈横纹肌肉瘤1例报告及文献复习

IF 0.2 Q4 PHARMACOLOGY & PHARMACY Asian Journal of Pharmaceutical Research and Health Care Pub Date : 2022-11-29 DOI:10.55561/ajhr.v2i2.118
T. Nurseta, Ayu Rizky Widowati
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引用次数: 0

摘要

子宫颈胚胎横纹肌肉瘤(RMS)是一种罕见的间质肿瘤,在所有宫颈癌中发生率不到1%。这些恶性肿瘤发生在青少年和年轻人身上。它起源于胚胎肌肉组织或多能间充质细胞。本病例报告一例罕见的33岁女性胚胎性横纹肌肉瘤。病例介绍:一位33岁的女性来到妇产科就诊。她主诉宫颈外生性肿块和阴道出血。病理组织学证实为子宫胚胎性横纹肌肉瘤(肉样肉瘤)。本病例采用根治性子宫切除术和辅助化疗相结合的治疗方案。结论:虽然成人宫颈横纹肌肉瘤的发病率很低,但为了获得良好的预后,多模式治疗是必要的。
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Rhabdomyosarcoma of The Uterine Cervix: Case Report and Literature Review
Introduction: Embryonal rhabdomyosarcoma (RMS) of the uterine cervix is a  rare mesenchymal tumor that occurs in less than 1% of all cervical cancers. These malignant tumors occur in adolescents and young adults. It starts from embryonic muscle tissue or pluripotent mesenchymal cells. This case reports an unusual case of embryonal rhabdomyosarcoma in a 33-year-old woman. Case Presentation: A 33-year-old woman came to the Obstetrics and Gynecology Department. She complained with exophytic cervical masses and vaginal bleeding. There were no remarkable findings about medical, family, and social history Histopathology confirms embryonal rhabdomyosarcoma (sarcoma botryoides) of the uterine cervix. A combination of radical hysterectomy and adjuvant chemotherapy was chosen as the therapeutic option in this case. Conclusion: Although the prevalence of cervical rhabdomyosarcoma in adults is very low, a multimodality approach is necessary for favorable prognostic.
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