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Uterine alveolar rhabdomyosarcoma in an elderly patient manifesting extremely poor prognosis; a rare subtype of rhabdomyosarcoma

机译:在一名老年患者中的子宫肺泡横纹肌肉瘤表现出极差的预后极差; rhabdomyosarcoma的罕见亚型

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摘要

Alveolar rhabdomyosarcoma (ARMS) arising in the corpus uteri is an extremely rare condition with exceptionally rapid progression and poor prognosis. Furthermore, ARMS is primarily diagnosed in the pediatric population. Due to rarity of the disease, there are no standard treatment guidelines. A 90-year-old woman was presented with a huge pelvic mass causing dyspnea and abdominal distension. The patient underwent debulking surgery and was diagnosed with uterine ARMS by fresh specimen biopsy. Despite intensive postoperative care, the patient died on the eighth postoperative day. Here, we report a case of uterine ARMS that will add to our understanding of this exceptionally rare type of tumor.
机译:在语料库中产生的肺泡横纹肌肉瘤(武器)是一种极其罕见的病症,进展迅速,预后差。此外,臂主要被诊断为儿科人群。由于遗憾的疾病,没有标准治疗指南。一个90岁的女性患有巨大的盆腔肿块,导致呼吸困难和腹胀。患者接受了脱脂手术,并通过新鲜标本活组织检查诊断患有子宫臂。尽管术后密切关心,但患者在术后第八天死亡。在这里,我们举报了子宫武器的情况,这将增加我们对这种异常罕见的肿瘤的理解。

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