Ayas Selçuk, Uygur Lutfiye, Bostanci Evrim, Gürbüz Ayşe
Department of Obstetrics and Gynecology, Zeynep Kamil Women and Children Diseases Research and Training Hospital, Turkey.
Department of Gynecology, Kadıköy Florence Nightingale Hospital, Turkey.
Iran J Reprod Med. 2015 Feb;13(2):113-6.
Sarcoma botryoides of cervix is a rare variant of rhabdomyosarcomas (RMS) of female genital tract. It is usually diagnosed in first or second decade of life. In this case report, we aimed to present a 21 year-old nulligravid patient who was diagnosed with embryonal RMS of the cervix, to discuss the treatment options that have been stated in the literature, and to highlight the advantage of fertility sparing management in these young patients.
We report a 21-year-old nulligravid woman complaining about a mass protruding from introitus, which was represented with a 8×7 cm "grape-like" cervical polyp on speculum examination. The histopathologic examination of the biopsy taken was combined with immunohistochemical staining with desmin, myogenin, S100, vimentin, and myoglobin. Colposcopy, second biopsy, and positron emission tomography were used during the follow-up. The histopathologic examination revealed embryonal RMS of cervix. She received three cycles of combination chemotherapy, doxorubicin and ifosfamide. She refused to have a surgery because of an unplanned, desired pregnancy at two months after the chemotherapy. She was lost during the follow-up. After having an uneventful pregnancy and a successful delivery, she reapplied at postpartum 6(th) month. Colposcopic evaluation revealed a local polypoid area, the histopathologic examination of biopsy suggested recurrence even though positron emission tomography scans were unremarkable. Therefore complementary treatment was planned as conization and pelvic lymphadenectomy. The histopathology revealed no residual tumor on the conization material and no involvement of pelvic lymph nodes.
Fertility sparing management, including doxorubicin and ifosfamid combination in chemotherapy step, can be management option. Pregnancy and successful delivery is possible during the treatment. Colposcopy has importance for early detection of recurrences.
宫颈葡萄状肉瘤是女性生殖道横纹肌肉瘤(RMS)的一种罕见变体。通常在生命的第一个或第二个十年被诊断出来。在本病例报告中,我们旨在介绍一名21岁未孕患者,她被诊断为宫颈胚胎性RMS,讨论文献中所述的治疗选择,并强调在这些年轻患者中保留生育功能管理的优势。
我们报告一名21岁未孕女性,主诉有肿物自阴道口突出,窥器检查显示为一个8×7 cm的“葡萄样”宫颈息肉。对所取活检组织进行组织病理学检查,并结合结蛋白、肌细胞生成素、S100、波形蛋白和肌红蛋白的免疫组化染色。随访期间进行了阴道镜检查、再次活检和正电子发射断层扫描。组织病理学检查显示为宫颈胚胎性RMS。她接受了三个周期的联合化疗,即阿霉素和异环磷酰胺。化疗两个月后,由于意外的、期望的妊娠,她拒绝接受手术。随访期间她失访了。在经历了一次顺利的妊娠和成功分娩后,她在产后第6个月再次就诊。阴道镜评估显示局部有息肉样区域,尽管正电子发射断层扫描无异常,但活检的组织病理学检查提示复发。因此,计划进行补充治疗,即锥切术和盆腔淋巴结切除术。组织病理学检查显示锥切标本无残留肿瘤,盆腔淋巴结未受累。
保留生育功能的管理,包括化疗步骤中使用阿霉素和异环磷酰胺联合治疗,可作为一种管理选择。治疗期间妊娠和成功分娩是可能的。阴道镜检查对于早期发现复发很重要。