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Small-Cell Neuroendocrine Carcinoma of the Cervix Masquerading as a Cervical Fibroid: Report of a rare entity

机译:宫颈伪装成宫颈肌瘤的小细胞神经内分泌癌:罕见实体的报告

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摘要

Primary neuroendocrine tumours of the cervix are extremely rare, with an incidence of only 0.5–1%; as such, these entities can present a clinical and diagnostic challenge. Small-cell neuroendocrine carcinomas of the cervix are highly aggressive tumours that have a tendency to metastasise. We report a 44-year-old woman who presented to the Gynaecology Clinic of the Employees State Insurance Corporation Medical College & Hospital, Faridabad, India, in 2016 with menorrhagia. Based on a clinical examination, she was provisionally diagnosed with a cervical fibroid. However, a biopsy revealed features of a small-cell neuroendocrine carcinoma of the cervix which was subsequently confirmed via immunohistochemistry. An accurate diagnosis of a neuroendocrine carcinoma is vital as it forms the basis for treatment decisions as well as informing predictions for long-term survival.
机译:子宫颈的主要神经内分泌肿瘤极少数,发病率仅为0.5-1%;因此,这些实体可以提出临床和诊断挑战。子宫颈的小细胞神经内分泌癌是高度侵蚀性的肿瘤,具有转移的趋势。我们举报了一位4名44岁的女性,他们介绍了员工状态保险公司医学院和医院的妇科诊所,2016年,Metorragia。基于临床检查,她被临时诊断出颈椎肌瘤。然而,活检显示宫颈的小细胞神经内分泌癌的特征,随后通过免疫组织化学证实。准确的诊断神经内分泌癌是至关重要的,因为它形成了治疗决策的基础以及了解长期存活的预测。

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